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Senior Scientist, Immunoproteomics, Mass Spectrometry (BS/MS)
Novartis
location-iconCambridge MA

6000! This is the number of associates in the Novartis Institutes for BioMedical Research (NIBR). This division is the innovation engine of Novartis, focusing on new technologies that have the potential to help produce therapeutic breakthroughs for patients. The Biologics Center (NBC) is accommodated within the Novartis Institutes for BioMedical Research (NIBR). NBC, in collaboration with the disease areas and technical expert groups, builds the future biologics therapy pipeline of Novartis through the discovery and creation of new antibody, protein, nucleic acid and virus-based molecules.We are in search of a Senior Scientist with expertise in protein mass spectrometry/quantitative proteomics in our Cambridge, MA location. Join the immunoproteomics team committed to support innovative biological drug discovery efforts and make a difference in lives.What you’ll be doing: Your responsibilities include, but are not limited to:• Immunogenicity assessment and profiling of biologics and new modalities using LC-MS for the identification of naturally processed MHC associated peptides.• Supporting mechanistic investigations of immunogenicity observed in patients• Supporting mechanistic understanding of molecule mode of action.• Supporting biotherapeutics candidate design/selection and assessment of new formats.• Addressing target specific mechanistic questions and increasing internal knowledge base.• Collaborate extensively across functional groups and a matrixed, cross-functioning team setting.• Present results in team meetings and deliver presentations to both small and large groups.This position will be located at the Cambridge, MA site and will not have the ability to be located remotely. This position will require 0% travel as defined by the business (domestic and/ or international).EEO StatementThe Novartis Group of Companies are Equal Opportunity Employers and take pride in maintaining a diverse environment. We do not discriminate in recruitment, hiring, training, promotion or other employment practices for reasons of race, color, religion, gender, national origin, age, sexual orientation, gender identity or expression, marital or veteran status, disability, or any other legally protected status. We are committed to building diverse teams, representative of the patients and communities we serve, and we strive to create an inclusive workplace that cultivates bold innovation through collaboration and empowers our people to unleash their full potential.Minimum requirementsWhat you’ll bring to the role: (required)• B.Sc. or M.Sc. with 5+ years relevant experience in academia or industry.• Hands-on mass spec experience (both in sample prep and LC-MS) and some level analysis is needed.• Experience in developing and performing proteomics experiments, nano LC-MS/MS, and analysis and interpretation of LC-MS/MS data using public and commercially available software (PEAKs, Proteome Discoverer, others).• Translate key scientific questions to essential proteomics experiments; design the study jointly with project team collaborators.• Self-motivated to explore new research areas, learn presentation skills and report writing, to further independently conducting and critically analyzing own research with minimal supervision.• Strong organization skills, verbal and writing communication skills for documentation of experiments, data analyses and communication of progress to manager and other team members.Desirable• Experience with quantitative proteomics (TMT, SILAC, label free), protein post-translational modification analysis, protein-protein-interaction analysis.• Experience with protein isolation from cells, tissue and biofluids. Immunoprecipitation or chemical affinity enrichment to selectively enrich proteins from complex biological samples.Why Novartis766 million lives were touched by Novartis medicines in 2021, and while we’re proud of this, we know there is so much more we could do to help improve and extend people’s lives.We believe new insights, perspectives and ground-breaking solutions can be found at the intersection of medical science and digital innovation. That a diverse, equitable and inclusive environment inspires new ways of working.We believe our potential can thrive and grow in an unbossed culture underpinned by integrity, curiosity and flexibility. And we can reinvent what's possible, when we collaborate with courage to aggressively and ambitiously tackle the world’s toughest medical challenges. Because the greatest risk in life, is the risk of never trying!Imagine what you could do here at Novartis!Commitment to Diversity & Inclusion:Novartis is committed to building an outstanding, inclusive work environment and diverse teams representative of the patients and communities we serve.Accessibility and Reasonable Accommodations: The Novartis Group of Companies are committed to working with and providing reasonable accommodation to individuals with disabilities. If, because of a medical condition or disability, you need a reasonable accommodation for any part of the application process, or in order to perform the essential functions of a position, please send an e-mail to tas.nacomms@novartis.com call +1 (877)395-2339 and let us know the nature of your request and your contact information. Please include the job requisition number in your message.Vaccine Policy (customer-facing roles only): While Novartis does not require vaccination for Covid-19 or proof of a recent negative test result for Covid-19 at this time, employees working in customer-facing roles must adhere to and comply with customers’ (such as hospitals, physician offices, etc.) credentialing guidelines, which may require vaccination. As required by applicable law, Novartis will consider requests for reasonable accommodation for those unable to be vaccinated. This requirement is subject to applicable state and local laws and may not be applicable to employees working in certain jurisdictions. Please send accommodation requests to Eh.occupationalhealth@novartis.com.DivisionNIBRBusiness UnitBIOLOGICS NIBRCountryUSAWork LocationCambridge, MACompany/Legal EntityNIBRIFunctional AreaResearch & DevelopmentJob TypeFull TimeEmployment TypeRegularShift WorkNoEarly TalentNo

Part Time / Full Time
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Partnerships Manager
Leyton USA Inc
location-iconBoston MA

Description:About Leyton: Leyton is a global consultancy firm dedicated to helping companies of all sizes improve their business performance with innovation funding through underutilized tax strategies and incentives. Founded in 1997, we have grown to over 2000 employees in 13 countries, with US offices in Boston and San Francisco. Having a newer US presence gives us the feel of a startup with the financial stability of a larger company. We offer real career opportunities in a fast-growing, friendly firm with a dynamic and ambitious team. With diverse groups from sales to scientists, there is plenty to learn and collaborate on - ideal for those who are intellectually curious. Our compensation package is competitive and you will be rewarded on the basis of your personal performance, as well as on the basis of the company's overall achievements. For the right candidate, the extensive growth plans for the US offer the opportunity to progress quickly. Function of the Role: Leyton is seeking a sales and partnerships professional motivated to build a diverse portfolio of complex CPA and channel partnerships. You will bring practical experience working with CPAs and possess leadership qualities to own and grow key industry relationships with unique deal dynamics. You will source, build and structure strategic selling opportunities, while negotiating agreements and managing the relationship. The ideal candidate will be operationally minded, a natural team player and solutions-oriented. More information on our partnerships can be found at https://leyton.com/us/partnerships/ Main Responsibilities Will Include: Meet with potential partners and take them through the sales cycle up to and including partner Certification Identify and evaluate new strategic business opportunities Structure potentially complex deal scenarios that may incorporate a sell-to or sell-with scenario involving multiple parties across an ecosystem Work effectively in a team environment and develop creative alternatives Generate holistic partnerships that are compelling business cases Build financial models to support complex deal negotiations Achieve sales, revenue and profit goals and strategies that advance the partnership performance Lead meetings on negotiating agreements and execute partnership plans Identify internal opportunities to improve sales effectiveness Coordinate cross-functionally to deliver process improvements, playbooks, toolkits, and skills development Requirements: Desired Skills & Experience: Business Development/Channel Sales/Partnership experience - minimum 3 years. Ideally with B2B sales experience in a services industry. Proven and successful track record in establishing strong and long-term customer relationships, being able to retain existing business and develop new business. Demonstrated ability to grow share in an Enterprise account High attention to detail and ability to work independently and efficiently on tasks, escalating when needed. Ability to lead negotiations and create and deliver high impact pitches. Excellent commercial acumen. Strong verbal and written communication and presentation skills; ability to speak to stakeholders at varying levels in an organization, tailoring your key message and being able to listen to the needs of their business. Ability to lead, develop, and motivate a senior team, leading them to surpassing of goals/targets Strong Financial acumen and P&L management experience Demonstrated ability to oversee partnership programs and deliver on the Leyton promise Demonstrated ability to effectively translate customer needs (expressed and unexpressed) into a successful account plan that drives growth in share of market Demonstrate high proficiency in MS Word, PowerPoint, and MS Excel, which are necessary for the creation of visually and verbally engaging reports and presentations for key stakeholders Minimum Bachelor's degree preferred CPA a strong asset What we offer you: Competitive salary, base + uncapped commission - OTE can surpass $150K with the uncapped commission component Career Growth Opportunities – we're growing, fast! A voice in strategy, process, and your professional growth Extensive Training Initial onboarding is comprehensive and robust. We're going to equip you with the knowledge and expertise you need to feel confidence on all of your client meetings. Reinforcement –continue to refine your skills with our sales training team Flexible and autonomous work environment Volunteer Opportunities Exposure to executive thought leaders with a passion for living our values Comprehensive Benefits including: Health Dental Vision Healthcare FSA HRA Generous vacation time 401k Pre-tax Transit & Parking plans Equal Employment Opportunity Policy Leyton provides equal employment opportunities to all employees and applicants for employment and prohibits discrimination and harassment of any type without regard to race, color, religion, age, sex, national origin, disability status, genetics, protected veteran status, sexual orientation, gender identity or expression, or any other characteristic protected by federal, state or local laws. This policy applies to all terms and conditions of employment, including recruiting, hiring, placement, promotion, termination, layoff, recall, transfer, leaves of absence, compensation and training. Physical Requirements: Prolonged periods of sitting at a desk and working on a computer. Must be able to lift 15 pounds at times. PM22PI202063169

Part Time / Full Time
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Medical Billing Specialist
LogixHealth
location-iconBedford MA

$5,000 Signing BonusThis Role:As a Billing Specialist at LogixHealth, you will work with a team of fellow medical billers, administrators, and coders to provide cutting edge solutions that will directly improve the healthcare industry. You’ll contribute to our fast-paced, collaborative environment and will bring your expertise to deliver exceptional third-party billing services.The ideal candidate will have strong technological skills, excellent interpersonal communication, and experience in third-party billing.Key Responsibilities:Review/work denials on an explanation of benefits (EOB) statementAnalyze A/R (Accounts Receivable) reports to follow up on unpaid claimsSend out appeals on claims that require an appealSubmit required documentation to insurance companies as requestedResearch claims for information in order to process bills in a timely mannerCommunicate with insurance companies, adjustors and patients on a regular basisCorrect errors and resubmit all unprocessed or returned claims to insurance companiesCreate UB92 and HCFA billsQualifications:To perform this job successfully, an individual must be able to perform each Key Responsibility satisfactorily. The following requirements are representative of the knowledge, skills, and/or ability required to perform this job successfully. Reasonable accommodation may be made to enable individuals with disabilities to perform the duties.Required:Ability to troubleshoot and remedy detailed documentsDemonstrated attention to detailAbility to perform data in billing softwareHigh School Diploma or equivalent combination of education and experiencePrior word processing, spreadsheet and internet software experience including proficiency with MS Excel and MS WordExcellent written and verbal communication skillsPreferred:Minimum of one year third party billing experienceHealthcare industry knowledgeAbility to read and interpret documents such as safety rules, operating and maintenance instructions and procedural manualsBenefits at LogixHealth:We offer a comprehensive benefits package including health, dental and vision, 401(k), PTO, paid holidays, life and disability insurance, on-site fitness center and company-wide social events.About LogixHealth:At LogixHealth we provide expert coding and billing services that allow physicians to focus on providing great clinical care. LogixHealth was founded in the 1990s by physicians to service their own practices and has grown to become the nation’s leading provider of unsurpassed software-enabled revenue cycle management services, offering a complete range of solutions, including coding and claims management and the latest business intelligence reporting dashboards for clients in 40 states.Since our first day, we have had a clear vision of a better healthcare system and have continually evolved to get there. In addition to providing expert revenue cycle services, we utilize proprietary software to provide valuable financial, clinical, and other data insights that directly improve the quality and efficiency of patient care.At LogixHealth, we’re committed to Making intelligence matter through our pillars of Physician-Inspired Knowledge, Unrivaled Technology and Impeccable Service.To learn more about us, visit our website https://www.logixhealth.com/.z2UdIfnjDF

Part Time / Full Time
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Volunteer Program and Training Coordinator
GTT, LLC
location-iconBoston MA

Volunteer Program and Training CoordinatorContract Duration 3-6 monthsHybrid (Mostly Onsite)Pay Range $23/Hr- $25/HrGeneral Summary Overview StatementWorking under the Direction of the Manager, The Program and Training Coordinator role is responsible for the recruitment, onboarding, and orientation of all new volunteers staff to the hospital.The role facilitates training for all hospital volunteers entering the Medical Career Exploration and department-specific training; Builds and maintains relationships with in-house departmental supervisors; Ensures ongoing communication with departments that are staffed with volunteers; and assists with hospital special events.Principal Duties And ResponsibilitiesVolunteer Program and Training Coordinator will conduct monthly New Volunteer Orientations (NVO).Conducts monthly Medical Career Exploration Program (MCEP) Orientations.Maintains Volunteer email box.Volunteer Program and Training Coordinator will conduct placement interviews for all volunteers to ensure eligibility and appropriate placement.Facilitates weekly Wayfinder training for Medical Career Exploration volunteers.Facilitates department-specific volunteer training such as the Emergency Department and the NICUVolunteer Program and Training Coordinator will provide support for assigned volunteers and department supervisors.Assists with the development of new volunteer programs and placements that align with HR and BWH strategic goals.Facilitates the process of eligible volunteers attending physician rounds.Oversees schedules and record keeping for volunteer programs.Oversees computer database in reference to relevant evaluations, demographic information, and statistical reports.Supports adherence to all required compliance and regulations (Joint Commission, DPH, PIPS, OHS, etc...)Assists with the coordination of hospital special events.Develops and maintains relationships with peer professionals and participants in local, regional, and national volunteer organizations.Skills And Abilities RequiredStrong interpersonal and organizational skills are essential.Strong presentation skillsAbility to work with people from diverse ethnic, cultural, educational, and socioeconomic backgrounds.Ability to work under pressure and in a busy office setting with many distractions.Experience in project coordination.Excellent listening and presentation skillsCustomer Service skills are essential.Writing skills are preferred.Creativity and an open-minded, professional attitudeQualificationsAt least two years of volunteer management or adult education.Competency in MS Word, PowerPoint, and ExcelBachelors preferredMust HavesVolunteer management or adult training experiencecompetency in MS Word, PowerPoint, and ExcelStrong customer service/ strong communication skillsWorking ConditionsProfessional, busy, office environment with limited privacy, many distractions, and a positive team-oriented atmosphere.Office Environment/HybridHours M-F 40 within business hoursAbout the CompanyOur client is a not-for-profit healthcare system that is committed to patient care, research, teaching, and service. The Company operates community and specialty hospitals, a managed care organization, a physician network, community health centers, home care, and other health-related entities. What sets our clients apart is their collaborative model of engagement. They work shoulder-to-shoulder with clients to continually improve their ability to deliver high-quality care and enhance their reputations. By developing long-term relationships, they are able to deliver targeted services and programs in strategy and planning, workforce training and education, quality improvement, and research development. The company has partnered with clients in more than 40 countries focusing on co-developing solutions that are tailored to the individual needs of their local healthcare systems.#ZR3#GTTDP

Part Time / Full Time
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Floating Community Manager
Bell Partners
location-iconBoston MA

We Care. We Deliver. Our purpose is to create communities our residents are proud to call home. We currently own or manage over 70,000 units in North America and continue to grow.Bell Partners, https://bellpartnersinc.com/overview/ a national leader in multi-family housing, our mission is to be the apartment company of choice by creating value and honoring commitments to our residents, partners, and associates.This position is responsible for leading and directing all community operations at a variety of locations throughout the region. The Community Manager leads and motivates community staff members to provide service to residents and maintain a high level of resident satisfaction.Essential Functions and Responsibilities:* Lead, direct, and control all facets of the community to ensure quality services and a high degree of customer satisfaction by to Bell Apartment Living standards and policies, while working within budgetary guidelines* Recruit, hire, manage and provide performance feedback to employees to ensure community performance and adequate staffing. Motivate associates through recognition programs, training, and team building* Train all staff members on proper leasing techniques and resident service* Conduct regular performance appraisals and address any associate concerns or employee relations issues. Maintain complete and accurate associate files and a high level of associate satisfaction, as measured by periodic surveys* Conduct weekly meetings with leasing and maintenance staff* Develop and administer the community budget* Evaluate unit prices in accordance with the market and budgeted goals* Develop an annual marketing plan and conduct marketing reviews on a monthly basis* Obtain bids for all contract services and oversee routine capital projects* Ensure that the onsite staff provides the highest level of service to residents* Responsible for 35% of leasing activitiesAdditional Functions and Responsibilities:* Additional duties as assignedKnowledge, Skills and Abilities:* Strong marketing skills required* Strong working knowledge of MS Office Suite to include MS Excel preferred* Yardi & Onesite knowledge preferred* Must demonstrate support of Bell Core Values* Must demonstrate ability to provide exceptional customer service* Must demonstrate ability to successfully work on a team* Must be able to clearly communicate both orally and in writing* Must be able to understand directives both orally and in writing* Must have superior interpersonal skills; ability to get along with diverse personalities; tactful; mature, flexible* Must present a professional image* Must be resourceful and well organized* Must be willing to travel as required within the assigned regionEducation and Background:* BA/BS in business, sales or related field, relevant experience or a combination* 3+ years’ experience in a property management role preferred#LI-DF1Bell Partners, Inc. (“BPI” or the “Company”) is an equal employment opportunity employer. BPI’s policy is not to discriminate against any applicant or employee based on race, color, sex, religion, national origin, age, disability, pregnancy, military/veteran status, marital status, genetic information, gender identity, sexual orientation or any other basis protected by applicable federal, state, or local laws. BPI also prohibits harassment of applicants or employees based on any of these protected categories. It is BPI’s policy to comply with all applicable state and federal laws respecting consideration of unemployment status in making hiring decisions.Note to Applicants: Smoking is prohibited in all indoor areas of Bell Partners Inc. unless designated smoking areas have been established by a particular location in accordance with applicable state and local law.Job Type: Full-time

Part Time / Full Time
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Project Manager - Hybrid
GTT, LLC
location-iconNorwood MA

Project Manager - HybridContract Duration 6+ monthsPay rate range $50 - $75/hrThe Role:The client is seeking an experienced Project Manager to join the team.In this role, the Project Manager will provide logistics support and oversight for a raw material shelf-life extension project.The individual will be responsible for coordinating activities and communication, both internally and with key suppliers, to ensure the timely completion of project milestones.The role requires a strong background in the management of cross-functional projects, attention to detail, and precise communication.Here's What You'll Do:Support a cross-functional team to ensure flawless execution of material shelf-life extension plans as stability studies complete key milestones.Collaborate with team members to create and maintain a detailed project plan.Coordinate recurring meetings with key suppliers to track progress toward key milestones.Proactively manage project risks and mitigation plans, and escalate when necessary.Maintain regular communication of progress with all project stakeholders.Prepare status updates for project review forums and communication to senior management.Initiate change controls and coordinate change action plans, ensuring that team members are held accountable for their actions.Coordinate change review board presentations with appropriate representation from the technical, supply chain, and quality team members.Manage shipment and tracking of raw materials to and from suppliers.Oversee re-labeling of materials and tracking of storage.Here's What You'll Bring to the Table:Education: University degree in an appropriate discipline (e.g., science, engineering, technology, business) Advanced degree (MS, Ph.D., MBA), and/or PMP is preferred.Minimum 5-10 years in pharmaceutical/biotechnology development and/or project management.The successful candidate will have demonstrated experience in leading cross-functional teams.Ability to work in a fluid environment and foster a strong collaborative spirit.Ability to negotiate and sustain networking relationships.Solid judgment with the ability to make good decisions.Excellent written and oral communication skills.Time management and organizational skills.Strong knowledge of project management tools/software (MS Project, SmartSheet, etc)About The Company:Our client is a globally diversified healthcare company with a central purpose to help people live their healthiest possible lives. They offer a broad portfolio of market-leading products that align with favorable long-term healthcare trends in both developed and developing markets. Working with this company, you'll tackle a wide array of problems including some of the world's greatest healthcare challenges while experiencing myriad cultures, geographies, and technologies. They are creating the future of healthcare through life-changing technologies and products that make you healthier and stronger, quickly identify when you have a medical need, and treat conditions to help you get back to doing what you love. It serves people in more than 160 countries with leading medical devices, diagnostics, nutrition products, and branded generic medicines.If you are looking for a great company to work for, look no further because our client has received an average of a four-star rating from its thousands of employees that have written positive reviews on Glassdoor and Indeed.#ZR1#GTTUS1

Part Time / Full Time
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Senior Research Programmer, Robotics Software Engineering
Boston Fusion
location-iconLexington MA

At Boston Fusion, we recognize diversity is the catalyst for limitless creativity. As a Senior Research Programmer in the Multi-Domain Systems directorate, you will utilize your knowledge of software engineering best practices and computer science skills to contribute and drive research efforts in development of autonomous and multi-agent distributed systems. This position requires a working knowledge of ROS (Robot Operating System) and 2-years experience with it. Every day, we go above and beyond to solve complex problems, making a difference for our nation. We do this by bringing together smart, curious people with diverse life experiences who collaborate creatively to achieve innovative technological breakthroughs. We are proudly building a work environment where you can bring your authentic self to work. Enjoy solving problems others think are unsolvable? Innovation and creative collaboration are at the center of everything we do. Working parent? We provide a hybrid work schedule and flexible working hours. Student? We offer education assistance and promote lifelong learning.   Due to the nature of our project work, we can only consider candidates with a current US Citizenship.   Featured Benefits: · Health Insurance: four plans to choose · Dental Insurance · LTD/STD · Relocation Assistance · Life Insurance · 401k 4% company match, vested immediately · Profit Sharing · Education Assistance · Hybrid Work Environment · Flexible Work Hours   Day-to-Day Responsibilities for Lead Scientist: Investigate fundamental topics in autonomous systems development, multi-agent distributed command and control, simulation to live drone software deployment, autonomous platform sensor fusion, and localized sensing Collaborate with the project team to provide technical and software design support to company research projects Collaborate with project/proposal team members to understand research direction and principles and provide guidance and input on technical design Provide technical leadership to several small or large project team(s) Provide technical mentorship to junior staff Utilize knowlede of current computer science theory, algorithms, and research to design solutions that meet the project requirements Utilize knowledge of a prefered domain area to design and implement the models developed by the scientists or others, as required Guide technical team on troubleshooting, debugging, and maintaining, existing software and provide solutions for improvement Maintain and advance knowledge of commercial and open-source off-the-shelf softwae packages, libraries, and frameworks that can be utilized in the software design Write software tests to validate code integrity Establish and maintain a professional rapport with all project stakeholders This job is right for you if you have (Minimum Qualifications): MS in Computer Science, Robotics Engineering, or related field, or equivalent work experience Expertise in Python, Java, and/or C++ 2+ years experience with ROS (Robot Operating System) Demonstrated successful experience on large-scale programming projects Ability to develp solutions to a variety of technical problems with limited guidance Excellent communication, writing, and presentation skills Ability to work under minimal direction Ability to work independently, as well as collaborate with team members Ability to multi-task, prioritize, and manage time effectively Excellent analytical and problem-solving skills Ability and desire to mentor junior staff PI202152483

Part Time / Full Time
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Biotransformation Sr Scientist, DMPK
Takeda
location-iconBoston MA

By clicking the "Apply" button, I understand that my employment application process with Takeda will commence and that the information I provide in my application will be processed in line with Takeda's Privacy Notice and Terms of Use . I further attest that all information I submit in my employment application is true to the best of my knowledge.Job DescriptionAbout the role:The DMPK department at Takeda, Cambridge, MA is seeking a highly motivated Sr Scientist to join the Drug Metabolism group. The primary responsibilities will be profiling and characterization of metabolites (small molecules, protein degrader, ASO, and/or siRNA)/catabolites (ADCs, proteins, and/or peptides) from complex biological matrices. A strong background in delineating biotransformation pathways and structural elucidation by LC-MS is required. A successful candidate must exhibit strong communication and interpersonal skills and desire to work in a fast-paced, flexible and dynamic environment. Experience with in vivo preclinical and clinical ADME studies and understanding of clearance route, mechanism and the role of metabolism/catabolism is essential.The position level will depend on the level of experience in the relevant areas.How you will contribute: ACCOUNTABILITIES Identification and structural elucidation of metabolites/catabolites of small molecules, protein degrader, ASO, siRNA, peptide, and protein drug candidates using LC-MS, NMR, and other structure elucidation tools.Hands on experience in operation, maintenance & trouble shooting of LC-MS, immune-capturing technology, and other instruments.Conduct in vitro drug metabolism studies of small molecules, protein degrader, payload release assays of ADCs, catabolism and stability assessment of peptide and protein drugs.,Conduct non-radio-labeled and radio-labeled metabolite profiling experiments from in vitro and in vivo studies (pre-clinical and clinical mass balance studies).Work independently, design experiments and report data in written reports and team presentations as required.Maintain accurate records of the study data.Minimum Requirements/Qualifications:Applicants should possess a PhD, MS, or BS in Organic/Analytical/Natural Products/Protein Chemistry with 3+ (PhD), 9+ years (MS) or 11+ years (BS) of pharmaceutical industry experience.Hands-on experience with HPLC and LC-MS are required. Familiarity with AB Sciex Q-TOF and/or Thermo Hybrid Orbitrap high resolution mass spectrometry instruments and metabolite identification is preferred.Good understanding of organic chemistry, structure elucidation and xenobiotic metabolismExperience in utilizing radiolabeled material in drug metabolism studies.Experience in analysis of protein degrader, ADC, ASO, and siRNA is a plus.Experience in immunocapture and protein/peptide analysis by LC-MS is a plus.Experience in metabolite/catabolite identification in in vitro systems (hepatocytes, microsome, etc.) and/or in vivo matrices (urine, feces, bile and plasma).The candidate must be able to analyze data and note significant deviations and maintain detailed, accurate and comprehensible study documentation.The individual is also expected to be highly organized, a team player, enthusiastic about drug discovery, and possess strong communication skills.Publications in peer-reviewed scientific journals are required.What Takeda can offer you:Comprehensive Healthcare: Medical, Dental, and VisionFinancial Planning & Stability: 401(k) with company match and Annual Retirement Contribution PlanHealth & Wellness programs including onsite flu shots and health screeningsGenerous time off for vacation and the option to purchase additional vacation daysCommunity Outreach Programs and company match of charitable contributionsFamily Planning SupportFlexible Work PathsTuition reimbursementMore about us:At Takeda, we are transforming patient care through the development of novel specialty pharmaceuticals and best in class patient support programs. Takeda is a patient-focused company that will inspire and empower you to grow through life-changing work.Certified as a Global Top Employer, Takeda offers stimulating careers, encourages innovation, and strives for excellence in everything we do. We foster an inclusive, collaborative workplace, in which our teams are united by an unwavering commitment to deliver Better Health and a Brighter Future to people around the world.In accordance with the CO Equal Pay Act, Colorado Applicants Are Not Permitted to Apply.EEO Statement Takeda is proud in its commitment to creating a diverse workforce and providing equal employment opportunities to all employees and applicants for employment without regard to race, color, religion, sex, sexual orientation, gender identity, gender expression, parental status, national origin, age, disability, citizenship status, genetic information or characteristics, marital status, status as a Vietnam era veteran, special disabled veteran, or other protected veteran in accordance with applicable federal, state and local laws, and any other characteristic protected by law. LocationsBoston, MAWorker TypeEmployeeWorker Sub-TypeRegularTime TypeFull time

Part Time / Full Time
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Biotransformation Sr Scientist, DMPK
Takeda Pharmaceutical
location-iconBoston MA

By clicking the “Apply” button, I understand that my employment application process with Takeda will commence and that the information I provide in my application will be processed in line with Takeda’s Privacy Notice and Terms of Use. I further attest that all information I submit in my employment application is true to the best of my knowledge.Job DescriptionAbout the role:The DMPK department at Takeda, Cambridge, MA is seeking a highly motivated Sr Scientist to join the Drug Metabolism group. The primary responsibilities will be profiling and characterization of metabolites (small molecules, protein degrader, ASO, and/or siRNA)/catabolites (ADCs, proteins, and/or peptides) from complex biological matrices. A strong background in delineating biotransformation pathways and structural elucidation by LC-MS is required. A successful candidate must exhibit strong communication and interpersonal skills and desire to work in a fast-paced, flexible and dynamic environment. Experience with in vivo preclinical and clinical ADME studies and understanding of clearance route, mechanism and the role of metabolism/catabolism is essential.The position level will depend on the level of experience in the relevant areas.How you will contribute:ACCOUNTABILITIESIdentification and structural elucidation of metabolites/catabolites of small molecules, protein degrader, ASO, siRNA, peptide, and protein drug candidates using LC-MS, NMR, and other structure elucidation tools.Hands on experience in operation, maintenance & trouble shooting of LC-MS, immune-capturing technology, and other instruments.Conduct in vitro drug metabolism studies of small molecules, protein degrader, payload release assays of ADCs, catabolism and stability assessment of peptide and protein drugs.,Conduct non-radio-labeled and radio-labeled metabolite profiling experiments from in vitro and in vivo studies (pre-clinical and clinical mass balance studies).Work independently, design experiments and report data in written reports and team presentations as required.Maintain accurate records of the study data.Minimum Requirements/Qualifications:Applicants should possess a PhD, MS, or BS in Organic/Analytical/Natural Products/Protein Chemistry with 3+ (PhD), 9+ years (MS) or 11+ years (BS) of pharmaceutical industry experience.Hands-on experience with HPLC and LC-MS are required. Familiarity with AB Sciex Q-TOF and/or Thermo Hybrid Orbitrap high resolution mass spectrometry instruments and metabolite identification is preferred.Good understanding of organic chemistry, structure elucidation and xenobiotic metabolismExperience in utilizing radiolabeled material in drug metabolism studies.Experience in analysis of protein degrader, ADC, ASO, and siRNA is a plus.Experience in immunocapture and protein/peptide analysis by LC-MS is a plus.Experience in metabolite/catabolite identification in in vitro systems (hepatocytes, microsome, etc.) and/or in vivo matrices (urine, feces, bile and plasma).The candidate must be able to analyze data and note significant deviations and maintain detailed, accurate and comprehensible study documentation.The individual is also expected to be highly organized, a team player, enthusiastic about drug discovery, and possess strong communication skills.Publications in peer-reviewed scientific journals are required.What Takeda can offer you:Comprehensive Healthcare: Medical, Dental, and VisionFinancial Planning & Stability: 401(k) with company match and Annual Retirement Contribution PlanHealth & Wellness programs including onsite flu shots and health screeningsGenerous time off for vacation and the option to purchase additional vacation daysCommunity Outreach Programs and company match of charitable contributionsFamily Planning SupportFlexible Work PathsTuition reimbursementMore about us:At Takeda, we are transforming patient care through the development of novel specialty pharmaceuticals and best in class patient support programs. Takeda is a patient-focused company that will inspire and empower you to grow through life-changing work.Certified as a Global Top Employer, Takeda offers stimulating careers, encourages innovation, and strives for excellence in everything we do. We foster an inclusive, collaborative workplace, in which our teams are united by an unwavering commitment to deliver Better Health and a Brighter Future to people around the world.In accordance with the CO Equal Pay Act, Colorado Applicants Are Not Permitted to Apply.EEO StatementTakeda is proud in its commitment to creating a diverse workforce and providing equal employment opportunities to all employees and applicants for employment without regard to race, color, religion, sex, sexual orientation, gender identity, gender expression, parental status, national origin, age, disability, citizenship status, genetic information or characteristics, marital status, status as a Vietnam era veteran, special disabled veteran, or other protected veteran in accordance with applicable federal, state and local laws, and any other characteristic protected by law.LocationsBoston, MAWorker TypeEmployeeWorker Sub-TypeRegularTime TypeFull time

Part Time / Full Time
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Scientist / Sr. Scientist, Bio Analytical Sciences
Omega Therapeutics
location-iconCambridge MA

Omega Therapeutics is a clinical-stage biotechnology company pioneering the first systematic approach to use mRNA therapeutics as a new class of programmable epigenetic medicines by leveraging its OMEGA Epigenomic Programming platform. The OMEGA platform harnesses the power of epigenetics, the mechanism that controls gene expression and every aspect of an organism's life from cell genesis, growth and differentiation to cell death. Using a suite of technologies, paired with Omega's process of systemic, rational and integrative drug design, the OMEGA platform enables control of fundamental epigenetic processes to correct the root cause of disease by returning aberrant gene expression to a normal range without altering native nucleic acid sequences. Omega's engineered, modular, and programmable mRNA-encoded epigenetic medicines, Omega Epigenomic Controllers , target specific intervention points amongst the thousands of mapped and validated proprietary and novel DNA-sequence-based epigenomic loci, EpiZips to durably tune single or multiple genes to treat and cure disease through Precision Genomic Control . Omega is currently advancing a broad pipeline of development candidates spanning a range of disease areas, including oncology, regenerative medicine, multigenic diseases including immunology, and select monogenic diseases. About the Role: Omega Therapeutics, Inc. is seeking a Scientist / Sr. Scientist, Bio Analytical Sciences (commensurate with experience) to join our Nonclinical Team. This person will support Discovery, Preclinical, and Clinical Development programs for bio analysis and will be responsible for developing and implementing PK and bio analytical strategy for programs, ensuring that PK and bio analytical support is completed in a timely, efficient manner and meets all current scientific and quality standards and adequately supports regulatory submissions. This person must be a scientifically motivated self-starter, capable of working with minimal supervision and is enthusiastic, detail oriented with a passion for bringing novel medicines to patients and comfortable working within a fast-paced scientific team. Key Responsibilities: Utilize significant scientific knowledge for design of bio analytical methods and algorithms to quantify the effect of LNP encapsulated RNAs on specific disease states both in Preclinical and Clinical areas Provide scientific and technical oversight to the bio analytical vendor for work performed at the CRO; manage assay development, transfer, troubleshooting, validation, and analysis of biological samples to support drug discovery & development for various candidates using LC-MS/MS, hybrid LC-MS/MS, qPCR, cell-based and ligand binding assays (ELISA, IHC) etc. at CRO Manage and resolve any problems or issues while keeping team and management informed of critical issues in a timely manner Responsible for ensuring reports are complete and accurate and meet regulatory filing requirements Responsible for preparing and/or providing input on Clinical/Non-Clinical regulatory documents including protocols, protocol amendments, reports, IBs, publications and presentations, and regulatory filings including IND etc., briefing books, and responses to questions from regulatory agencies Expected to advise teams and management continuously and proactively on the development and optimization of bioanalytical technologies, strategies and models to improve the quality and productivity of the function Will be a member of the Early Development/Nonclinical Safety group but will partner with colleagues in other functional areas such as Clinical Operations/Development etc. as needed to identify and manage external vendor support of GLP/GCP sample analysis Will also be required to stay current with the latest in technological and regulatory advances in the bio analytical realm Required Qualifications: MS with 8+ years of experience or PhD with 5+ years of experience Strong expertise in FDA/EMA, GLP/GCP regulatory requirements and both Clinical & Non-Clinical bio analytical data management (both GLP and non-GLP) including data transferring, analysis, and reporting Prior experience with laboratory and vendor management is required Strong organization, multi-tasking and communication skills are key attributes of the successful candidate Individuals with regulatory writing experience in the context of bio analytical sciences, and having first-author, peer reviewed publications and/or presentations will be strong candidates for this role

Part Time / Full Time
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GSB Finance & Analysis Northeastern Co-op
Boston Consulting Group
location-iconBoston MA

WHAT YOU'LL DO​​We are seeking one position to support the Global Specialty Businesses Finance team. We are looking for a student who is self-motivated and can excel in project based work. This includes support in the preparation of monthly reporting, owning the timesheet & expense reimbursement auditing process and managing the file maintenance system within Oracle as it relates to project and employee based reporting. The majority of this role is performing various ad hoc reporting and projects to support GSB management as well as the various Finance Business Partners on the team.​YOU'RE GOOD AT​​Organized, detail oriented and analytical ​Interpersonal and communication skills. ​Being proactive and resourceful ​Taking initiative with limited direction ​Ability to work in a fast paced environment​ YOU BRING (EXPERIENCE & QUALIFICATIONS)​​Strong MS Excel skills, proficient in other MS office ​Preference for someone working on a BS/BA in Business or Finance ​Preferably a middler or sophomore with strong academic performance ​Prior work/ co-op experience preferable​ Must meet the Co-op program eligibility requirements of the current college/university’s academic department and student must be approved by the college/university to participate in the Co-op program. Must be an undergraduate currently enrolled in the Northeastern University Co-op Program Must have legal work authorization in the U.S. Must be physically located in the U.S. during Co-op Must be able to work Eastern Time Zone business hours Monday-Friday YOU'LL WORK WITH​​The GSB finance team is anchored in BCG’s worldwide finance organization and falls under the GSB Finance Director. The primary responsibility of the GSB Finance team is to partner with the specialty businesses to provide financial insight with accurate and meaningful analysis. ​GSB is a unique part of BCG that acts a bit like a start-up. Because of this, the co-op has a completely unique experience that they wouldn't be able to get in any other Finance roles. The co-op supports the entire Global Specialty Businesses Finance team working with different levels of employees/management in locations across the globe. ADDITIONAL INFORMATIONCandidates should be aware that BCG currently maintains a policy requiring all US & Canada based employees to be fully vaccinated against COVID-19. Newly hired employees must be fully vaccinated prior to their employment start date. BCG is an equal opportunity employer and will provide a reasonable accommodation to those unable to be vaccinated for medical or religious reasons where it is not an undue hardship to the company to do so as provided under applicable federal, state, provincial and local law.

Part Time / Full Time
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Account Executive (CT, RI, MA, NY)
Imagine Learning
location-iconBoston MA

Great Purpose. Great People. Great Opportunities.At Imagine Learning we ignite learning breakthroughs. It drives everything we do. We innovate together to support educators in creating those special moments when students experience the joy of learning at its best.  We also ignite career breakthroughs, with the majority of our positions being fully remote opportunities that offer you what you’re really looking for: flexible work arrangements, interesting and meaningful job responsibilities, career growth, and a supportive team.  Imagine Your Impact.The Account Executive is instrumental in helping grow the company by finding leads, closing sales, supporting existing clients, formulating sales strategies, and communicating product value to clients. Living in Providence, RI, MA, NY or CT, or planning to relocate to these states, is required. Position Type: This is a regular, full-time position.Compensation: Base pay is anticipated to be between $74,058 and $85,000 per year. Eligible employees may also receive incentive/commission/annual bonus pay based on individual and/or company performance. Compensation may vary based on factors such as, but not limited to, individual skills, experience, training, education/certifications, geographic location, internal equity, and local market conditions.Location: In this US-based position your location will be remote out of your home office in RI, CT, NY, or MA.Travel: You can also expect up to 75% travel, so be sure you have a valid driver’s license and automobile insurance and a clean driving record for at least the preceding 39 months.  Envision Your Experience.In this role you’ll have the opportunity to:Provide support for districts by learning about and satisfying their needs.Make cold calls or reach out to prospects.Follow up with prospects several times throughout the sales cycle to ensure needs are being met.Present and demonstrate the value of products and services to prospective buyers.Compile and analyze data to find trends and outcomes.Develop sales strategies and set quotas.Stay current on company offers and industry trends.Maintain a database of contact information and monthly forecastBuild long-lasting, mutually beneficial relationships with external contacts and internal departments to create a world-class customer experience.Handle complaints and negotiations.Other duties as required. Share Your Expertise.Experience, education, and qualifications essential for success in this role, include:Bachelor’s degree in business, marketing, or related field and at least 7-10 years of external sales-related experience; or an acceptable combination of education and experience.Comprehensive and current knowledge of company offerings and industry trends or ability to quickly learn.Excellent verbal and written communication skills.Ability to understand client needs and handle the negotiation process.Strong time management skills with the ability to multi-task and meet demanding deadlines.Strong Computer skills, including MS Office, MAC, CRM software, and Social Media platforms.Drive and energy to manage multiple accounts while looking for new opportunities. Ignite Your Career. Imagine Learning is committed to fostering, cultivating, and preserving a culture of Diversity, Equity, and Inclusion. We support your unique career journey by providing flexibility, investing in wellbeing, and propelling growth.  We offer a flexible workplace, with the majority of employees enjoying the opportunity to work from home within the US. Headquartered in Scottsdale, AZ, we also maintain offices in Austin, TX, Petaluma, CA, and Rock Rapids, IA. Imagine Learning provides a comprehensive benefits program to eligible employees, including:Multiple health, dental, and vision plans, including medical plans with zero employee premiums 401k plan with a company matchCompany-paid behavioral health coaching15 paid holidays, including 2 floating holidays and a winter shutdown from Christmas Eve through New Year’s Day15 days of accrued annual Paid Time Off (PTO) Fertility benefitsPaid bonding leave when a new child joins your family    Life and short and long-term disability insurancePre-tax savings plansPaid volunteer hours and annual giving eventsA wide variety of professional development programs, including tuition reimbursement  Imagine Learning is an Equal Opportunity Employer committed to a diverse workforce, providing equal employment and advancement opportunities to qualified individuals. All qualified applicants will receive consideration for employment without regard to race, color, religion, gender, gender identity or expression, sexual orientation, national origin, genetics, disability, age, veteran status, or any other protected status. Imagine Learning will reasonably accommodate qualified individuals as required by law.

Part Time / Full Time
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Senior Compliance Manager
Actalent
location-iconBedford MA

Great Opportunity to get your foot in the door with one of the top pharmaceutical companies in the Billrica area!If interested please reach out to asimboli@actlenetservices.comif interested please reach out to Description:• Implement electronic Quality Systems, such as eQMS, EDMS, and LMS, providing procedures and training for employees to effectively use the electronic Quality Systems• Design, plan, implement, and manage documentation programs, policies, and procedures that support company objectives and regulatory requirements• Supervise the QA Documentation department in the creation, issuance, maintenance, archiving, and storage of cGMP and cGXP-controlled documentation and records• Manage electronic document processing, retrieval, and distribution systems (EDMS), electronic learning management systems (LMS), electronic Quality Management Systems (TrackWise), etc.• Administer document and system access rights and revision control to ensure the security of the system and the integrity of master documents• Lead Monthly Quality Review Board (QRB) meetings, Quality Investigation Board (QIB)• Supervise the creation of an annual training calendar and other training initiatives at the site• Provide expertise and input to other functional areas affecting controlled documents and records• Assist with FDA and other compliance audits including corporate audits.• Facilitate and follow up with stakeholders with regard to responses to audit observations• Prepare annual internal audit schedule and perform execution of same• Oversee site vendor management program including performing annual vendor risk assessment• Oversee harmonization efforts between corporate and plant Quality procedures and policies• Provide QA review of Annual Product Reviews (APRs) to identify trends and recommend CAPA as needed• Provide QA review of quality events such as unplanned/planned deviations and change controls• Participate in investigation team efforts to determine the root cause for critical quality events and recommend appropriate CAPA• Develop presentation materials for upper management to disseminate on the topics of quality issues, QMSinitiatives, and related projects• Participate in Regional Quality related projects and initiatives, acting as an ambassador between corporate and plant• Issuance of Quality Alerts, FAR/Recall as per internal proceduresSkills:cms, quality management system, tracks, root cause analysis, CAPA, edms, product compliance, complaint handlingTop Skills Details:qms, quality management system,trackwise,root cause analysis,capa,edmsAdditional Skills & Qualifications:• BS in chemistry or a related scientific field • Minimum ten (10) years of related experience in pharmaceutical (manufacturing) environment, biotech industry, Quality Assurance, Quality Control and/or production, or FDA-regulated industry.• Strong working knowledge of a Quality Management System (QMS) and adherence to 21 CFR Parts 210, 211; aseptic drug manufacturing experience a plus• Superior internal and external customer service/people skills• Ability to manage multiple responsibilities and training projects in a fast-paced environment, in an efficient manner • Ability to present self in a professional, credible manner and communicate effectively at all levels of the organization• Ability to prioritize and organize own work, multi-task, meet deadlines and keep commitments• Experience in developing and managing various types of training initiatives expected • Excellent administrative & organization skills• Strong presentation and MS PowerPoint Skills • Positive attitude; values others and works well independently and in a team environment• Excellent verbal, written, and interpersonal communication skills• Works under minimal supervision following established procedures along with own judgment.• Expert knowledge of electronically based Quality Systems• Working knowledge of pharmaceutical and medical device documentation and change controls • Experience with continuous improvement programs and project management skills • Working knowledge of applicable domestic and international standards and regulationsExperience Level:Expert Level About Actalent: Actalent connects passion with purpose. Our scalable talent solutions and services capabilities drive value and results and provide the expertise to help our customers achieve more. Every day, our experts around the globe are making an impact. We’re supporting critical initiatives in engineering and sciences that advance how companies serve the world. Actalent promotes consultant care and engagement through experiences that enable continuous development. Our people are the difference. Actalent is an operating company of Allegis Group, the global leader in talent solutions. The company is an equal opportunity employer and will consider all applications without regards to race, sex, age, color, religion, national origin, veteran status, disability, sexual orientation, gender identity, genetic information or any characteristic protected by law.

Part Time / Full Time
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Senior Finance Programmer Analyst
Cornerstone Research
location-iconBoston MA

Overview:SENIOR BUSINESS SYSTEMS ANALYST(HYBRID/ON-SITE, SAN FRANCISCO, SILICON VALLEY, LOS ANGELES, CHICAGO, BOSTON, NEW YORK, WASHINGTON D.C.)If you are Business Systems Analyst looking for an opportunity to showcase your Business & Financial Systems administration, then we would like to meet with you!The Senior Business Systems Analyst will have primary responsibility for leading various analysis and programming initiatives in Cornerstone Research’s IT application department utilizing their knowledge of business analysis and financial reporting.At Cornerstone Research, you will be part of a thriving, 700-strong team that spans eight offices, comprises more than 40 nationalities, and leads the industry in its commitment to develop team members across all levels. Inc. Magazine has recognized Cornerstone Research three times as a Best Workplace for its outstanding employee engagement, collaborative culture, and professional growth opportunities.You’ll Love It Here If YouEmbrace learning and continuous improvementSet and strive for a high bar of excellenceBelieve that teamwork leads to success: ask us what it means to be #onefirmfirm!Take pride in always doing your best work, even if it’s harder or takes longerAre passionate about what you doHow You’ll Help Our Team SucceedPerform business systems analysis and support of company-wide IT business applications and ensure the successful performance of financial systems by performing systems analyst activities and making recommendations in areas that require a high level of technical competency.Operate as the primary resource for financial and billing reporting from the Aderant system, including the maintenance of standard reports, the modification of existing reports, and the creation of new reports.Work with the Financial Reporting team in Finance and IT in developing Cornerstone’s reporting strategy to determine scalable and appropriate solutions for the variety of financial reporting requests.Design and implement business intelligence solutions to support the decision makers and users of the data by utilizing, but not limited to, SQL Server Integration Services (SSIS), SQL Server Analysis Services (SSAS), SQL Server Reporting Services (SSRS), and Power BI.Maintain the financial systems, including the time and accounting system, payroll, fixed assets, budgeting, and financial reporting systems.Customize reports and the user interface in Aderant Expert, including advanced scripting in Summit Basic, using the customization tools in Aderant Expert.What You’ll Need to Be Successful8-10 years of experience that demonstrates increasing capability and responsibility; professional services experience preferred.8+ years of experience with SQL and T-SQL programming7+ years of experience working with Aderant, including super-user capabilities, SQL Server 2008/2012/2019, SSAS, SSRS, and SSIS, and other hands-on financial systems experience3+ years of experience working with and translating company financial data into executive-level reports and KPIs2+ years of experience in Power BIThe desire to take initiative and actively contribute to the team and the firmThe ability to communicate effectively and professionallyStrong business acumen and the ability to learn the firm’s financial and operational functionsThe mindset to provide superior serviceMS SQL report and Visual Basic programming experienceAdvanced MS Office skills - especially Excel, including macro development/troubleshootingExperience in providing technical support for Workday, Chrome River, IridiumExperience with web development technologies using C#, Microsoft .NET technologiesExperience integrating diverse systems such as Workday and LDAPAbility to successfully engage in multiple tasks simultaneouslyBachelor’s degree or demonstrated equivalent combination of education, training, and experienceWho We AreCornerstone Research provides economic and financial analysis and expert testimony in all phases of commercial litigation and regulatory proceedings.We work with a broad network of testifying experts, including leaders from academia and industry, who are recognized for their depth of knowledge, accomplishments, and research. Our staff consultants contribute expertise in economics, finance, accounting, and marketing, as well as business acumen, familiarity with the litigation process, and a commitment to produce outstanding results.The firm’s uniquely collegial and supportive atmosphere makes Cornerstone Research a great place to work. We invest in our people in a host of ways, from providing meaningful learning and development opportunities to organizing memorable social events. To many, our culture and our people are the most exciting and enriching aspects of a career at Cornerstone Research.Equal Employment OpportunityCornerstone Research is an equal employee opportunity employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, pregnancy, age, national origin, disability, sexual orientation, gender identity or expression, marital status, genetic information, protected veteran status, or other factors protected by law.

Part Time / Full Time
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Sr. Microsoft Stack Developer
ConsultNet
location-iconBoston MA

Title: Sr. Microsoft Stack DeveloperLocation: Remote (San Francisco, Boston, New York)Type: Direct Hire/Fulltime w/ClientJob Description:ConsultNet has a great non-profit client actively looking for a full-time Sr. Microsoft Stack DeveloperWe are looking for someone with 7+ years developing within Microsoft StackC#, .Net, HTML, CSS, SQL, MS Dynamics and Azure Logic Apps.We are looking for someone who can design, document, build, test and deploy Dynamics CRM Online enhancementsCan collaborate within Agile/ Scrum environmentsMust be able to customize out-of-the-box solutionsRequired Skills:7+ years of MS Stack DevelopmentDynamics CRM, Azure, C#, .Net, CSS, HTMLBonus/Soft Skills:Exposure to Non-ProfitsBe a part of the ConsultNet difference. As a leading national provider of IT staffing and solutions, ConsultNet delivers exceptional services to startup, midmarket and Fortune 1000 companies across North America. Since 1996, we've partnered with clients to create rewarding opportunities for our consultants, successfully building teams that have surefire results.In the past two years alone, we have placed more than 1,500 consultants in contract, contract-to-hire, or direct placement opportunities. We understand communication is key to finding the right job that matches your skills and career goals. For us, it's not just the work that we do; it's how we do the work. Our breadth of offerings extends to multiple IT positions in major markets throughout the country, see more at -

Part Time / Full Time
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Document Control Coordinator - hybrid
Yoh
location-iconBoston MA

Document Control Coordinator needed for a contract opportunity with Yoh's client in Boston, MA. Top Skills You Should Possess:High School diploma or equivalent and 3+ years of document control experience.Proficient with MS Office (Word, Excel, PowerPoint) and Adobe. What You'll Be Doing:Pay range: $ 22.00 to $ 25.00 per hour, depending on experience and qualifications.Hybrid position (onsite 2 days a week).Performs daily document deposits for Accounting and Finance related business units.Upload in scope documents to Enterprise Contract Management Solution (ECMS) for several GCF business units.Track, update, and distribute expected documents report (EDR) for daily and monthly changes.Perform monthly KPI/KRI Reporting.Perform other ad-hoc projects assigned by manager. What You Need to Bring to the Table:High School diploma or equivalent and 3+ years of document control experience.Proficient with MS Office (Word, Excel, PowerPoint) and Adobe.Good communication and interpersonal skills.Reliable, team player. Recruiter: Cliff RussoNote: Any pay ranges displayed are estimations. Actual pay is determined by an applicant's experience, technical expertise, and other qualifications as listed in the job description. All qualified applicants are welcome to apply.Yoh, a Day & Zimmermann company, is an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, or status as a protected veteran.Visit to contact us if you are an individual with a disability and require accommodation in the application process.

Part Time / Full Time
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Research Associate II/Senior RA, Bioanalytical Product Development
Entrada Therapeutics
location-iconBoston MA

The OrganizationWhat's happening at Entrada Therapeutics? Our mission is to transform the treatment of devastating diseases and improve patients' quality of life using intracellular biologics. Leveraging our proprietary Endosomal Escape Vehicle (EEV) platform, we are creating and advancing a diverse pipeline of oligonucleotide, enzyme, protein and peptide programs to efficiently target and engage underlying drivers of diseases.Our novel approach to drug design and delivery addresses current challenges associated with both large and small molecule therapeutics and represents a fundamental advancement in the field of intracellular biologics.We're a tight-knit team of experts and leaders in both therapeutics development and rare disease and are excited to grow and attract colleagues who are ready to join a high energy, dedicated team that likes to get things done and dramatically improve the lives of patients and their families.The Perfect FitYou should be versatile, self-motivated, and looking forward to rolling up your sleeves, as you'll be a member of the product development team. You'll thrive in our team by working closely with scientists to provide bioanalytical support to various modalities including oligonucleotides and proteins, to perform quantitative bioanalysis in complex biological matrices, and to actively participate in the process of exploring, investigating, and implementing innovative technologies to facilitate program progress. You'll also get the opportunity to be involved in the collaboration with CROs to support for pre-IND and IND enabling studies. You'll have the opportunity to contribute to scientific publications and regulatory submissions as needed.You should also enjoy a fast-paced environment and juggling competing priorities. You follow up and follow through, connecting problems with solutions efficiently. You work successfully in a team environment with strong interpersonal skills to effectively build working relationships inside and outside the company.The OpportunityWork within the bioanalytical team to enable the full spectrum of EEV-derived modalities development from early discovery candidate selection to late-stage process development.You ResponsibilitiesPerform sample extraction and sample analysis using established LC-MS/MS methods to support PK, biodistribution and biomarker studies.You guys Coordinate sample storage, inventory, data analysis and interpretation; present results in internal team meetings.Assist in bioanalytical assays development and qualification including LC-MS/MS, ELISA and enzymatic assays to support quantification/characterization of EEV-derived therapeutics in various biological matricesRecord experiments and procedures in laboratory/electronic notebooks, execute assays with good documentation practices.Collaborate within and cross functional teams to facilitate program progress.The NecessitiesAt Entrada, our passion for science, our devotion to patients and our values drive our behavior:Humanity - We genuinely care about patients and about one another.Tenacity - We are relentless and persistent in the pursuit of developing therapies for patients.Creativity - We are creative problem solvers.Collaboration - We are more than the sum of our parts.Curiosity - We have a growth mindset and push conventional thought and theory.To thrive on our team, you will need to come with:A bachelor's or Master's degree in chemistry, biochemistry, pharmacology, biomedical engineering or related fields with 2+ years of experience in R&D laboratory, preferably in an industrial setting.Demonstrated experience in standard analytical skills and data analysis.Experience with RP-H/UPLC and MS techniques for compound characterization and quantitation is highly desirable.Hands-on experience with biological sample (urine, plasma, tissue, etc.) handling and preparation.Strong communication skills (oral and written) and the ability to work effectively in a multidisciplinary team.Desire to work in an innovative and collaborative environment pursuing high reward science The PerksBy becoming a team member here at Entrada, you'll have access to competitive health, dental, and vision coverage, as well as life insurance, and short term and long-term disability insurance. We value work life balance, you'll benefit from discretionary time off, paternity leave, and an excellent 401(k) package. We also offer a generous transportation stipend to commute as you wish. Our location in the vibrant and growing Seaport District is close to all the best that the city of Boston has to offer. Entrada Therapeutics is an equal opportunity employer. Qualified candidates will receive consideration for employment without regard to race, color, religion, national origin, gender, sexual orientation, gender identity or expression, age, mental or physical disability, and genetic information, marital status, citizenship status, military status, protected veteran status or any other category protected by law. Third Party Staffing AgenciesEntrada does not accept unsolicited resumes from any source other than directly from candidates. For the protection of all parties involved in the recruiting process, resumes will only be accepted from recruiters/agencies if a signed agreement is in place at the inception of the recruiting effort and authorized for a specified position. Unsolicited resumes sent to Entrada from recruiters/agencies do not constitute any type of relationship between the recruiter/agency and Entrada and do not obligate Entrada to pay fees if we hire from those resumes.

Part Time / Full Time
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Administrative Assistant
CaptiveAire
location-iconBoston MA

Company Description:CaptiveAire is the nation's leading manufacturer of commercial kitchen ventilation systems, and now provides a complete solution of fans, heaters, ductwork, and HVAC equipment. For over 40 years, we've led the industry with innovative technologies, unmatched service, competitive pricing, and rapid lead times.CaptiveAire maintains a network of over 90 sales offices in the U.S. and Canada and six strategically located manufacturing plants in North Carolina, Iowa, Oklahoma, California, Pennsylvania and Florida.Summary:This position will provide administrative support to allow our field technicians to focus on their high volume of service calls. The individual will be responsible for administrative support, scheduling, and preventative maintenance services (sales) for a growing service department.Job Description:Administrative DutiesHigh volume phone calls and emailsUpdating service team calendarsFor completion/submission such as tax exemption forms, vendor packets, and insurance requestsParts requestsMeter calibration trackingSchedulingIntake and scheduling of service requests from customersCoordinate scheduling changes and enter notes of local service teamsPreventative Maintenance Service SalesContact customers on behalf of service regionsWork with local service team on PM quotesAgreement tracking and remewalsPersonal Requirements:Excellent data entry and organizational skillsVery close attention to detail and accuracyStrong Written and verbal communication skillsAble to work with minimal supervisionKnowledge and Skills Requirements:High school diploma, 2- or 4- year degree preferred2-5 years' experience in customer service or administrative focused role; HVAC industry is preferred but not requiredExperience with MS Office, proficiency in ExcelSalary: Base salary (above average), plus monthly bonus based upon productivity and profits.Captive-Aire Systems, Inc. is proud to be an equal opportunity workplace. We review applications for employment without regard to their race, color, religion, sex, sexual orientation, gender identity, national origin, ancestry, citizenship, age, uniformed services, genetic information, physical or mental disability, medical condition, marital status, or any other basis prohibited by law.

Part Time / Full Time
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Research Assistant - Chemistry LAB Operations
Labcorp
location-iconBedford MA

Explore research careers and be a part of something bigger as a Research Assistant for the Analytical Lab Operations in Bedford, MA! Labcorp Drug Development helps to develop new drugs, medical devices and diagnostics. Your role is vital to improving the health of family, friends and animals. As a Research Assistant I you will be responsible for providing technical expertise in supporting preclinical studies conducted under GLP, ISO 17025, and various other regulatory agencies. Research Assistants must work closely with study directors, analytical services staff, and quality assurance to ensure all study aspects are conducted in per scientific and regulatory requirements.  Excellent communication skills needed as this position works closely with other research associates and scientists.  Individual must be highly organized to handle multiple projects on an ongoing basis. Additional responsibilities include, but are not limited to: Performing routine analysis and troubleshooting utilizing various analytical instruments, specifically HPLC, LC/MS (single quad, Orbitrap, etc.), etc. Experience in interpretation of MS data and compound identification requiredFamiliarity with LC instrument maintenance Experience with methods of sample preparation of solid and liquid samples in a variety of matrix types for LC analysisExperience with analytical method validation is a plusReview data and prepare summary results for reportingAssist in managing inventory for all laboratory supplies Review and assist Study Director and Quality Assurance in closing out any protocol amendments, or deviations and work to ensure compliance with all applicable regulatory guidelinesMeet project deadlines including the completion of technical work to applicable protocols and standards Experience with other analytical instrumentation including, GC/FID, GC/MS, and TOC preferredEducation/Qualifications/Experience:Bachelor of Science/Arts (BS/BA) degree in chemistry or related scientific field. Relevant Bioanalytical experience may be substituted for education. Must have some knowledge of GMP/GLP regulations in an analytical laboratory settingAbility to work in a fast paced environmentAbility to perform basic computer skills (e. g., Word, Excel). Familiar with the use of standard laboratory equipment (e. g., balances, pipettes, centrifuges). Experience with analytical instrumentation. Able to effectively communicate, both verbally and in writing. How will you be rewarded! Enjoy 24 days of personal-time-off (PTO) (pro-rated based on start date) AND Additional Paid Holidays. Have access to other great benefits including: 401(k) plan with a generous company match and of course medical, vision and dental insurance and much more! Labcorp is proud to be an Equal Opportunity Employer:As an EOE/AA employer, Labcorp strives for diversity and inclusion in the workforce and does not tolerate harassment or discrimination of any kind. We make employment decisions based on the needs of our business and the qualifications of the individual and do not discriminate based upon race, religion, color, national origin, gender (including pregnancy or other medical conditions/needs), family or parental status, marital, civil union or domestic partnership status, sexual orientation, gender identity, gender expression, personal appearance, age, veteran status, disability, genetic information, or any other legally protected characteristic. We encourage all to apply. For more information about how we collect and store your personal data, please see our Privacy Statement.  

Part Time / Full Time
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Principal Cloud Engineer - Data
Magna International Inc.
location-iconBoston MA

Group Description At Magna, we create technology that disrupts the industry and solves big problems for consumers, our customers, and the world around us. We’re the only mobility technology company and supplier with complete expertise across the entire vehicle. We are committed to quality and continuous improvement because our products impact millions of people every day. But we’re more than what we make. We are a group of entrepreneurial-minded people whose collective expertise gives us a competitive advantage. World Class Manufacturing is a journey and it’s our talented people who lead us on this journey.   Key Responsibilities Design and build robust, high-performance, and adaptable solution optimal for modern highly scalable platform (Big Data/Relational/No-SQL/OLAP) with ability to integrate technical functionality Research, evaluate, architect, and deploy new tools, frameworks, and patterns to build sustainable Big Data platforms. Responsible for the delivery of a robust scalable data architecture that meets the business goals of the organization. Provide technical thought leadership on High Level Architecture and Design, data modeling, Big Data strategy & adoption for Ingestion and Analytics Applications Lead the architecture, design, development of the business intelligence platform Define technical principles, vision, and standards for the data warehouse Ensure the design can scale to handle additional data demands Key Qualifications/Requirements BS or MS (MS Preferred) in Statistics, Physics, Math, Computer Engineering, Computer Science or Electrical Engineering with 12-14 years of work experience. 5 years of experience in a Cloud Engineering managing data. Thorough understanding of data tools like Amazon Redshift, Databricks, Snowflake Good grasp of tools like Spark Expert as Analytical Products as a Service Resident expertise in data handling best practices, archiving, compression, serialize/de-serialize methods Strong experience (5+ years) with Amazon Web Services, Azure or Google Cloud Platform and all supporting technologies. Awareness. Unity. Empowerment. At Magna, we believe that a diverse workforce is critical to our success. That’s why we are proud to be an equal opportunity employer. We hire on the basis of experience and qualifications, and in consideration of job requirements, regardless of, in particular, color, ancestry, religion, gender, origin, sexual orientation, age, citizenship, marital status, disability or gender identity. Magna takes the privacy of your personal information seriously. We discourage you from sending applications via email to comply with GDPR requirements and your local Data Privacy Law.

Part Time / Full Time
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Senior Scientist, Immunoproteomics, Mass Spectrometry (BS/MS)
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Part Time / Full Time
location-iconCambridge MA
Job Description
6000! This is the number of associates in the Novartis Institutes for BioMedical Research (NIBR). This division is the innovation engine of Novartis, focusing on new technologies that have the potential to help produce therapeutic breakthroughs for patients. The Biologics Center (NBC) is accommodated within the Novartis Institutes for BioMedical Research (NIBR). NBC, in collaboration with the disease areas and technical expert groups, builds the future biologics therapy pipeline of Novartis through the discovery and creation of new antibody, protein, nucleic acid and virus-based molecules.

We are in search of a Senior Scientist with expertise in protein mass spectrometry/quantitative proteomics in our Cambridge, MA location. Join the immunoproteomics team committed to support innovative biological drug discovery efforts and make a difference in lives.

What you’ll be doing: Your responsibilities include, but are not limited to:
• Immunogenicity assessment and profiling of biologics and new modalities using LC-MS for the identification of naturally processed MHC associated peptides.
• Supporting mechanistic investigations of immunogenicity observed in patients
• Supporting mechanistic understanding of molecule mode of action.
• Supporting biotherapeutics candidate design/selection and assessment of new formats.
• Addressing target specific mechanistic questions and increasing internal knowledge base.
• Collaborate extensively across functional groups and a matrixed, cross-functioning team setting.
• Present results in team meetings and deliver presentations to both small and large groups.

This position will be located at the Cambridge, MA site and will not have the ability to be located remotely. This position will require 0% travel as defined by the business (domestic and/ or international).

EEO Statement

The Novartis Group of Companies are Equal Opportunity Employers and take pride in maintaining a diverse environment. We do not discriminate in recruitment, hiring, training, promotion or other employment practices for reasons of race, color, religion, gender, national origin, age, sexual orientation, gender identity or expression, marital or veteran status, disability, or any other legally protected status. We are committed to building diverse teams, representative of the patients and communities we serve, and we strive to create an inclusive workplace that cultivates bold innovation through collaboration and empowers our people to unleash their full potential.

Minimum requirements

What you’ll bring to the role: (required)
• B.Sc. or M.Sc. with 5+ years relevant experience in academia or industry.
• Hands-on mass spec experience (both in sample prep and LC-MS) and some level analysis is needed.
• Experience in developing and performing proteomics experiments, nano LC-MS/MS, and analysis and interpretation of LC-MS/MS data using public and commercially available software (PEAKs, Proteome Discoverer, others).
• Translate key scientific questions to essential proteomics experiments; design the study jointly with project team collaborators.
• Self-motivated to explore new research areas, learn presentation skills and report writing, to further independently conducting and critically analyzing own research with minimal supervision.
• Strong organization skills, verbal and writing communication skills for documentation of experiments, data analyses and communication of progress to manager and other team members.

Desirable
• Experience with quantitative proteomics (TMT, SILAC, label free), protein post-translational modification analysis, protein-protein-interaction analysis.
• Experience with protein isolation from cells, tissue and biofluids. Immunoprecipitation or chemical affinity enrichment to selectively enrich proteins from complex biological samples.

Why Novartis
766 million lives were touched by Novartis medicines in 2021, and while we’re proud of this, we know there is so much more we could do to help improve and extend people’s lives.

We believe new insights, perspectives and ground-breaking solutions can be found at the intersection of medical science and digital innovation. That a diverse, equitable and inclusive environment inspires new ways of working.

We believe our potential can thrive and grow in an unbossed culture underpinned by integrity, curiosity and flexibility. And we can reinvent what's possible, when we collaborate with courage to aggressively and ambitiously tackle the world’s toughest medical challenges. Because the greatest risk in life, is the risk of never trying!
Imagine what you could do here at Novartis!

Commitment to Diversity & Inclusion:
Novartis is committed to building an outstanding, inclusive work environment and diverse teams representative of the patients and communities we serve.

Accessibility and Reasonable Accommodations: The Novartis Group of Companies are committed to working with and providing reasonable accommodation to individuals with disabilities. If, because of a medical condition or disability, you need a reasonable accommodation for any part of the application process, or in order to perform the essential functions of a position, please send an e-mail to tas.nacomms@novartis.com call +1 (877)395-2339 and let us know the nature of your request and your contact information. Please include the job requisition number in your message.

Vaccine Policy (customer-facing roles only): While Novartis does not require vaccination for Covid-19 or proof of a recent negative test result for Covid-19 at this time, employees working in customer-facing roles must adhere to and comply with customers’ (such as hospitals, physician offices, etc.) credentialing guidelines, which may require vaccination. As required by applicable law, Novartis will consider requests for reasonable accommodation for those unable to be vaccinated. This requirement is subject to applicable state and local laws and may not be applicable to employees working in certain jurisdictions. Please send accommodation requests to Eh.occupationalhealth@novartis.com.

Division

NIBR

Business Unit

BIOLOGICS NIBR

Country

USA

Work Location

Cambridge, MA

Company/Legal Entity

NIBRI

Functional Area

Research & Development

Job Type

Full Time

Employment Type

Regular

Shift Work

No

Early Talent

No
job-detail-figure
Senior Scientist, Immunoproteomics, Mass Spectrometry (BS/MS)
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Part Time / Full Time
location-iconCambridge MA
Job Description
6000! This is the number of associates in the Novartis Institutes for BioMedical Research (NIBR). This division is the innovation engine of Novartis, focusing on new technologies that have the potential to help produce therapeutic breakthroughs for patients. The Biologics Center (NBC) is accommodated within the Novartis Institutes for BioMedical Research (NIBR). NBC, in collaboration with the disease areas and technical expert groups, builds the future biologics therapy pipeline of Novartis through the discovery and creation of new antibody, protein, nucleic acid and virus-based molecules.

We are in search of a Senior Scientist with expertise in protein mass spectrometry/quantitative proteomics in our Cambridge, MA location. Join the immunoproteomics team committed to support innovative biological drug discovery efforts and make a difference in lives.

What you’ll be doing: Your responsibilities include, but are not limited to:
• Immunogenicity assessment and profiling of biologics and new modalities using LC-MS for the identification of naturally processed MHC associated peptides.
• Supporting mechanistic investigations of immunogenicity observed in patients
• Supporting mechanistic understanding of molecule mode of action.
• Supporting biotherapeutics candidate design/selection and assessment of new formats.
• Addressing target specific mechanistic questions and increasing internal knowledge base.
• Collaborate extensively across functional groups and a matrixed, cross-functioning team setting.
• Present results in team meetings and deliver presentations to both small and large groups.

This position will be located at the Cambridge, MA site and will not have the ability to be located remotely. This position will require 0% travel as defined by the business (domestic and/ or international).

EEO Statement

The Novartis Group of Companies are Equal Opportunity Employers and take pride in maintaining a diverse environment. We do not discriminate in recruitment, hiring, training, promotion or other employment practices for reasons of race, color, religion, gender, national origin, age, sexual orientation, gender identity or expression, marital or veteran status, disability, or any other legally protected status. We are committed to building diverse teams, representative of the patients and communities we serve, and we strive to create an inclusive workplace that cultivates bold innovation through collaboration and empowers our people to unleash their full potential.

Minimum requirements

What you’ll bring to the role: (required)
• B.Sc. or M.Sc. with 5+ years relevant experience in academia or industry.
• Hands-on mass spec experience (both in sample prep and LC-MS) and some level analysis is needed.
• Experience in developing and performing proteomics experiments, nano LC-MS/MS, and analysis and interpretation of LC-MS/MS data using public and commercially available software (PEAKs, Proteome Discoverer, others).
• Translate key scientific questions to essential proteomics experiments; design the study jointly with project team collaborators.
• Self-motivated to explore new research areas, learn presentation skills and report writing, to further independently conducting and critically analyzing own research with minimal supervision.
• Strong organization skills, verbal and writing communication skills for documentation of experiments, data analyses and communication of progress to manager and other team members.

Desirable
• Experience with quantitative proteomics (TMT, SILAC, label free), protein post-translational modification analysis, protein-protein-interaction analysis.
• Experience with protein isolation from cells, tissue and biofluids. Immunoprecipitation or chemical affinity enrichment to selectively enrich proteins from complex biological samples.

Why Novartis
766 million lives were touched by Novartis medicines in 2021, and while we’re proud of this, we know there is so much more we could do to help improve and extend people’s lives.

We believe new insights, perspectives and ground-breaking solutions can be found at the intersection of medical science and digital innovation. That a diverse, equitable and inclusive environment inspires new ways of working.

We believe our potential can thrive and grow in an unbossed culture underpinned by integrity, curiosity and flexibility. And we can reinvent what's possible, when we collaborate with courage to aggressively and ambitiously tackle the world’s toughest medical challenges. Because the greatest risk in life, is the risk of never trying!
Imagine what you could do here at Novartis!

Commitment to Diversity & Inclusion:
Novartis is committed to building an outstanding, inclusive work environment and diverse teams representative of the patients and communities we serve.

Accessibility and Reasonable Accommodations: The Novartis Group of Companies are committed to working with and providing reasonable accommodation to individuals with disabilities. If, because of a medical condition or disability, you need a reasonable accommodation for any part of the application process, or in order to perform the essential functions of a position, please send an e-mail to tas.nacomms@novartis.com call +1 (877)395-2339 and let us know the nature of your request and your contact information. Please include the job requisition number in your message.

Vaccine Policy (customer-facing roles only): While Novartis does not require vaccination for Covid-19 or proof of a recent negative test result for Covid-19 at this time, employees working in customer-facing roles must adhere to and comply with customers’ (such as hospitals, physician offices, etc.) credentialing guidelines, which may require vaccination. As required by applicable law, Novartis will consider requests for reasonable accommodation for those unable to be vaccinated. This requirement is subject to applicable state and local laws and may not be applicable to employees working in certain jurisdictions. Please send accommodation requests to Eh.occupationalhealth@novartis.com.

Division

NIBR

Business Unit

BIOLOGICS NIBR

Country

USA

Work Location

Cambridge, MA

Company/Legal Entity

NIBRI

Functional Area

Research & Development

Job Type

Full Time

Employment Type

Regular

Shift Work

No

Early Talent

No