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Title Researcher and Right of Way Specialist
Maverick Construction Corp
location-iconBoston MA

Title Researcher / Right-of-Way Specialist Maverick Corporation is a full-service Engineering and Construction firm working in the telecommunications and electrical power sectors. Our customers range from traditional municipal and co-op electric utilities and telecommunication service providers to companies operating in the oil & gas and the transportation industries. Maverick Corporation and its affiliates provide project management, quality control and review services; aerial, underground, and technical services in construction; as well as design, survey, permitting, and owner's agent services in engineering. Maverick has been incorporated since 1994, and is a growing company with headquarters in Boston, Massachusetts. Maverick is seeking a Title Researcher/Right of Way Specialist to support our growing engineering team headquartered in Boston, MA with offices across the country. The ideal candidate will have experience working in the telecommunication, electrical engineering, and/or real estate fields. It shall require the ability to operate in a fast-paced environment assisting in researching and outlining requirements to successfully permit overhead and underground designs. This person will work closely with management for design, field, permitting, and GIS teams to establish a common understanding of the rights to land use and processes. Responsibilities: Identifies encroachment, trespass, and land use conflicts Research title abstracts, deeds, and other data to determine boundaries and property rights Performs rights assessments, identify record errors, gaps in rights, project permit needs Coordinates work activities to support projects as assigned Assisting in obtaining licenses, permits, or other as needed Maintains and updates the Company's records/ database Provides technical support and assistance to operating areas relative to ROW land management as assigned Assists property right negotiations for the acquisition and disposition of property rights as assigned or directed Performs vendor coordination as required Responds to questions relating to land use codes by the client and project team Maintain tracking spreadsheets as needed Collaborate with project team to appropriate actions Qualifications: Associates or bachelor's degree in engineering, real estate, GIS, other related field, OR comparable professional experience Experience with AutoCAD, ArcMap, and 3GIS or other mapping software is preferred Proficient in MS Excel and/or similar spreadsheet applications Creative and analytical mind with a willingness to learn Must enjoy working in a fast paced, high-growth, and rapidly changing work environment Highly flexible in daily duties and level of responsibility Excellent oral and written communication skills Previous utility engineering experience is a plus Permitting or GIS experience is a plus Successful completion of pre-employment drug & alcohol and background check requirements Benefits Ability to participate in the Company Health Care/ Dental / Vision programs FSA/HSA plans available when you participate in Health Care plan Ability to participate in the Long Term and Short-Term Disability Policy Life Insurance covering one year's salary up to $100K Ability to participate in Company 401K retirement account, Maverick will match up to 4% percent of your base pay Salaried employees accrue 2 weeks paid time off each year PI192192113

Full Time
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Partnerships Manager
Leyton USA Inc
location-iconBoston MA

Description: 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:Will be responsible for identification, evaluation and execution of strategic selling opportunities through channel sales partnerships with a focus on CPAs, alliances, and inbound/outbound marketing initiatives. You'll bring practical experience in sourcing complex CPA partnerships and deal dynamics that ultimately shape a win-win scenario for the parties involved to significantly accelerate the growth trajectory of Leyton US.Will source, build and structure potentially complex partnerships negotiating agreements and executing partnership plans taking them through the sales cycle. You will seek out and partner with venture capital/private equity firms, industry associations and key business influencers. 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 CertificationIdentify and evaluate new strategic business opportunitiesStructure potentially complex deal scenarios that may incorporate a sell-to or sell-with scenario involving multiple parties across an ecosystem.Work across partner ecosystem to build/lead cross functional teams in support of deal structuring -- Work effectively in a team environment and develop creative alternatives.Generate holistic (partnership) compelling business cases (Build financial models to support complex deal negotiations), think strategically and act on ideas, and effectively sell these ideas to the leadership team.Achieve sales, revenue and profit goals and strategies that advance the partnership performance and enables the achievement of the departments' as well as the business's financial goalsLead meetings on negotiating agreements and execute partnership plans.Identify 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 2-3 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 accountHigh 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/targetsStrong Financial acumen and P&L management experienceDemonstrated ability to oversee partnership programs and deliver on the Leyton promiseDemonstrated ability to effectively translate customer needs (expressed and unexpressed) into a successful account plan that drives growth in share of marketDemonstrate 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 stakeholdersMinimum Bachelor's degree preferredCPA a strong assetWhat we offer you:Competitive salary, base + uncapped commission - OTE can surpass $150K with the uncapped commission componentCareer Growth Opportunities – we're growing, fast!A voice in strategy, process, and your professional growthExtensive 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 teamFlexible and autonomous work environmentVolunteer OpportunitiesExposure to executive thought leaders with a passion for living our valuesComprehensive Benefits including:HealthDentalVisionHealthcare FSAHRAGenerous vacation time401kPre-tax Transit & Parking plansEqual 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. PM22PI192432408

Full Time
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Title Researcher and Right of Way Specialist
Maverick Construction Corp
location-iconBoston MA

Title Researcher / Right-of-Way Specialist Maverick Corporation is a full-service Engineering and Construction firm working in the telecommunications and electrical power sectors. Our customers range from traditional municipal and co-op electric utilities and telecommunication service providers to companies operating in the oil & gas and the transportation industries. Maverick Corporation and its affiliates provide project management, quality control and review services; aerial, underground, and technical services in construction; as well as design, survey, permitting, and owner’s agent services in engineering. Maverick has been incorporated since 1994, and is a growing company with headquarters in Boston, Massachusetts.Maverick is seeking a Title Researcher/Right of Way Specialist to support our growing engineering team headquartered in Boston, MA with offices across the country. The ideal candidate will have experience working in the telecommunication, electrical engineering, and/or real estate fields. It shall require the ability to operate in a fast-paced environment assisting in researching and outlining requirements to successfully permit overhead and underground designs. This person will work closely with management for design, field, permitting, and GIS teams to establish a common understanding of the rights to land use and processes. Responsibilities: Identifies encroachment, trespass, and land use conflictsResearch title abstracts, deeds, and other data to determine boundaries and property rightsPerforms rights assessments, identify record errors, gaps in rights, project permit needsCoordinates work activities to support projects as assignedAssisting in obtaining licenses, permits, or other as neededMaintains and updates the Company’s records/ databaseProvides technical support and assistance to operating areas relative to ROW land management as assignedAssists property right negotiations for the acquisition and disposition of property rights as assigned or directedPerforms vendor coordination as requiredResponds to questions relating to land use codes by the client and project teamMaintain tracking spreadsheets as neededCollaborate with project team to appropriate actionsQualifications: Associates or bachelor’s degree in engineering, real estate, GIS, other related field, OR comparable professional experienceExperience with AutoCAD, ArcMap, and 3GIS or other mapping software is preferredProficient in MS Excel and/or similar spreadsheet applicationsCreative and analytical mind with a willingness to learnMust enjoy working in a fast paced, high-growth, and rapidly changing work environmentHighly flexible in daily duties and level of responsibilityExcellent oral and written communication skillsPrevious utility engineering experience is a plusPermitting or GIS experience is a plusSuccessful completion of pre-employment drug & alcohol and background check requirementsBenefitsAbility to participate in the Company Health Care/ Dental / Vision programsFSA/HSA plans available when you participate in Health Care planAbility to participate in the Long Term and Short-Term Disability PolicyLife Insurance covering one year’s salary up to $100KAbility to participate in Company 401K retirement account, Maverick will match up to 4% percent of your base paySalaried employees accrue 2 weeks paid time off each yearPI192130932

Full Time
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Operations Analyst, Sales
Perch Energy
location-iconBoston MA

Description: Perch Energy is a whole new kind of energy company focused on providing and promoting more access to green and affordable energy for all. We believe business can and should be a force for good. Perch Energy was recently spun out of BlueWave Solar and is in the midst of building our own Company while scaling our Community Solar offering and releasing other exciting products to help people access clean, green energy.Perch Energy has an immediate opening for an Operations Analyst, Sales, reporting to the VP of Sales. With direct handling of the customer acquisition process and an emphasis on enrollment and contract processing, you will onboard Sales Partners and assist in the management of customer applications. Your role focuses on identifying how to improve the customer acquisition process and equip Sales Partners with the necessary tools to educate customers on the community solar product. The role covers customer enrollment, managing partner commission payments, and using data to identify sales trends across multiple partners, utility territories, and solar projects. The ideal candidate is motivated, driven, dependable, and thrives in a fast-paced, team-oriented environment. Duties & ResponsibilitiesProcess and underwrite customer contracts according to state, utility, and client requirements according to company metricsPrioritize project fulfillment needs and assign deal flow to projects to ensure on-time fill rates Create and drive structured customer data auditing to ensure maintained accuracy and completion of data in CRMResearch channel commission, billing, and enrollment inquiries and coordinate with appropriate departments for resolutionTriage and manage incoming partner requests and inquiries regarding the community solar subscription programSupport Sales leaders in operationalizing sales-related tasksProvide sales channels with daily reporting to socialize churned and rejected customers, enrolled customers, and commission reportsParticipate in the review of sales channel commission reports to ensure accuracy and payment timelinessCreate cases or tickets to resolve sales channel and customer-related issuesCreate sustainable processes to increase efficiency in customer contract underwriting, and maintain updated process documents over timeSupport the overall objectives of the company, and especially the sales organization, to ensure the success of the individual manager, the team, and the company Ad hoc processes upon request Requirements: Skills and Qualifications2+ years of operations experiencePrior enrollment or contract processing experienceKnowledge of Salesforce or other CRM a plus but not requiredStrong oral and written communication skillsStrong attention to detailExcellent interpersonal skillsProficient with Excel, MS Word, PowerPoint, etc. What does it mean to be a Percher?It means you want a day job that makes a difference—and you're all in on building extraordinary products that get us there. It means you think big. Act fast. Assume value. And it means you can count on us to look out for you while you do it—in a place you can find your tribe.Benefits that help you live your best lifeLooking out for you means looking out for the whole person you are—from health and financial wellbeing to awesome benefits for work-life balance.Medical, dental & vision—stay healthy and perceptiveStock options & 401K— prepare for the futureLife insurance, short and long-term disability—plan for the unexpectedHealth savings account (HSA) match—get pre-tax saving coverageUnlimited paid time off—take time to fuel upPerch is proud to be an Equal Employment Opportunity (EEO) employer. We are committed to creating a diverse and inclusive workplace and will do so by actively seeking to hire and promote diverse individuals throughout the company. Providing equal employment opportunities to all employees and applicants for employment is critical to our identity and we do not discriminate on the basis of race, color, religion, religious creed, national origin, ancestry, sex, age, handicap (disability), sexual orientation, gender identity/ or expression, genetics, veteran status, marital status, pregnancy or pregnancy-related condition, military status or obligation, or other protected status, in accordance with applicable federal, state and local laws.PI192525999

Full Time
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LC/MS-MS Method Development Scientist
Eurofins USA
location-iconWaltham MA

Eurofins Scientific is an international life sciences company, providing a unique range of analytical testing services to clients across multiple industries, to make life and our environment safer, healthier and more sustainable. From the food you eat, to the water you drink, to the medicines you rely on, Eurofins works with the biggest companies in the world to ensure the products they supply are safe, their ingredients are authentic and labelling is accurate.Eurofins is the global leader in food, environment, pharmaceutical and cosmetic product testing and in agroscience Contract Research Organisation services. Eurofins is one of the market leaders in certain testing and laboratory services for genomics, discovery pharmacology, forensics, advanced material sciences and in the support of clinical studies, as well as having an emerging global presence in Contract Development and Manufacturing Organisations. The Group also has a rapidly developing presence in highly specialised and molecular clinical diagnostic testing and in-vitro diagnostic products.In over just 30 years, Eurofins has grown from one laboratory in Nantes, France to 55,000 staff across a decentralised and entrepreneurial network of 900 laboratories in over 50 countries. Eurofins offers a portfolio of over 200,000 analytical methods to evaluate the safety, identity, composition, authenticity, origin, traceability and purity of biological substances and products.In 2020, Eurofins generated total revenues of EUR € 5.4 billion, and has been among the best performing stocks in Europe over the past 20 years.Job DescriptionHigh-res LCMSMS method development for global profiling of lipids in biological samples.Work with analytical instrumentation, especially with LC – High Resolution Mass spectrometry, LC-MS/MS methodology for targeted analysis of lipids and other endogenous biomolecules (including proteins); the knowledge of  analytical work in the regulated environment .Build Lipid data bases and analysis of lipid pathways.Conduct biomarker validation studies within industry standards for identification and validation of biomarkers.Maintenance, cleaning, tuning and troubleshooting of advanced mass spectrometers (triple quadrupole and high resolution Orbitrap mass specs).Development and implementation of LC-MS profiling methods, and quantitative analysis of endogenous biomolecules.Conduct experiments for elucidation of structures for metabolic biomarkers.Work with Compound Discoverer, Progenesis, Mass Profiler Professional and Expressionist platforms for processing of metabolomics and proteomics data.Utilization of publically available Lipid data bases, especially Lipid Maps.Analyze and report on affected metabolic pathways.Develop internal biomarkers database and metabolomics data processing software.Develop high-res LCMSMS methods for specific biomarkers in biological matrices and analyze samples as required.Apply analytical results to target credentialing and mechanism of action studies, phenotypic screens, design of in-vitro studies and establishment of disease biomarkers.Develop LV-High Resolution MS and LC-MS/MS methods for global profiling of lipids in biological samples. Carry out analysis of the affected metabolic pathways and report the data to the project teams.Participate in the work of client’s metabolomics team by contributing in development of internal biomarkers data base, and metabolomics data processing software, including collaborating with instrument/software vendors.Conduct metabolic biomarker discovery work which will guide teams supporting high priority projects by LC-High Res MS methodology KPI: provide timely updates and results summary in the form of oral presentations, PowerPoint summaries, Excel reports, and custom reports generated in Client’s data processing platform.Develop and run targeted LC-MS/MS methods for analysis of identified lipid markers in biological samples.Support client’s target credentialing and mechanism of action studies, establishment of phenotypic screens, establishment and validation of animal models as well as clinical studies with Lipidomics and targeted lipid analysis and LC-MS analysis of proteins.Participate in establishment of disease biomarkers suitable for monitoring of disease progression and effectiveness of treatment.Upon need for support of establishment and conducting LC-MS based phenotypic screens using multiplex LC-MS instruments.QualificationsBachelor's Degree in science related discipline and 6 years of experienceMaster's Degree in science related discipline and 3 years of experiencePhD Candidates are encouraged to apply Experience with LC/MS/MS method developmentExperience building Lipid data bases and analysis of lipid pathwaysAdditional InformationPosition is full-time, Monday - Friday 8:00am - 5:00pm.  Candidates currently living within a commutable distance of Waltham, MA and the surrounding areas are encouraged to apply.Excellent full time benefits including comprehensive medical coverage, dental, and vision optionsLife and disability insurance401(k) with company matchPaid vacation and holidaysEurofins is a M/F, Disabled, and Veteran Equal Employment Opportunity and Affirmative Action employer.

Full Time
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Sr. Scientist - Lipidomics
Yoh, A Day & Zimmermann Company
location-iconCambridge MA

Job DescriptionSr. Scientist – Lipidomics Why Yoh? Yoh knows greater talent, that’s why. In the Analytical Testing Department, we are looking for a highly motivated Sr. Scientist to join us in LC-MS/MS method development, optimization, and implementation.This role would suit a successful Scientist that has experience with LC/MS/MS method development, having experience building Lipid data bases and analysis of lipid pathways is a plus.Yoh is in a unique position, we have to find the best technical talent, provide services to some of the world’s largest companies, and be a great employer. We do that with the great people we have working for us. This Sr. Scientist - Lipidomics opportunity is with our client in the Cambridge, MA area. The role is for a direct-hire opportunity with a competitive salary and benefits package, relocation assistance, and a monthly transportation stipend. This client is globally recognized as a leader in providing analytical testing services to clients across multiple industries both nationally and internationally.  We strive to be a company that embraces diversity, is inclusive, and thrives on learning so that our employees feel respected and invited to contribute to the success of our company, clients, suppliers, and communities.Your ContributionEssential FunctionsLC-MS/MS method development, optimization and implementation.Work with analytical instrumentation, especially with Triple quadrupole Mass spectrometers (preferably Sciex)Ability to work with LC-High Resolution MS is a plusMaintenance, cleaning, tuning and troubleshooting of the mass spectrometersExcellent bench skills, especially sample preparationDevelopment and implementation of LC-MS methods, for characterization and quantitative analysis.Experience with Lipidomic and Metabolomic analyses is a plus Your AccomplishmentsRequired SkillBachelor's Degree in science related discipline and 6 years of experienceMaster's Degree in science related discipline and 3 years of experiencePhD Candidates are encouraged to apply Experience with LC/MS/MS method developmentExperience building Lipid data bases and analysis of lipid pathways is a plus Your Benefits & CompensationCompensation $93,000-$104,000, Depending on experienceDirect Hire Opportunity!BenefitsRelocation StipendMonthly Transportation StipendMedical, Dental & Vision Benefits401K Retirement Saving PlanLife & Disability InsurancePerformance Incentives Opportunity is Calling, Apply Now! | Recruiter: Amber Meza, Amber.Meza@yoh.com   Yoh makes finding and applying for jobs simple. Partner with Yoh to find the right opportunities across multiple industries in the US and UK. Find out more hereYoh, 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 https://www.yoh.com/applicants-with-disabilities to contact us if you are an individual with a disability and require accommodation in the application process.

Full Time
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Global Strategic Alliances Co-op
Boston Consulting Group
location-iconBoston MA

WHAT YOU'LL DOWe are seeking one position to support the Global Strategic Alliances team. We are looking for a student who is self-motivated and can excel in project based work. This includes supporting database management & analytics and preparation of pipeline reporting. The role will require liaising with internal & external stakeholders, BCG client teams, marketing & occasionally DigitalBCG leadership. The balance of this role is performing various ad hoc projects to support GSA management team in advancing our operations and Go To Market agenda. This role interfaces with BCG technology experts & consulting colleagues so the candidate needs to have excellent communication skills & be able to work with discretion.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 environmentYOU BRING (EXPERIENCE & QUALIFICATIONS)• Strong MS Excel skills, proficient in other MS office• Preference for someone working on a BS/BA or MS/MA in Business, Marketing, Finance or Technology• Preferably a senior student with strong academic performance• Prior work/ co-op experience required• 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• BCG is currently allowing remote work situations in the U.S. due to COVID-19, however should this change, applicants must be able to be physically present in the BCG Boston office (if required by BCG/Hiring Manager) within a reasonable timeframe.YOU'LL WORK WITHGlobal Strategic Alliances are a key part of continuing to progress the way the firm meets the ever-evolving needs of clients and markets, through collaborative partnerships, with the largest and most relevant technology and services companies. The team comprises of the Global Alliances Director and supporting Managers who oversee the program through pillars of brand build, program management, capability build, business development and go to market initiatives. The team is dedicated to commercializing our growing number of strategic alliance partnerships and market-facing opportunities across practice areas, industries, geographies, KDPs, as well as Digital.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.

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

Full Time
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Metabolomics Scientist
Yoh, A Day & Zimmermann Company
location-iconCambridge MA

Job DescriptionSr. Scientist Metabolomics LCMS Why Yoh? Yoh knows greater talent, that’s why. In the Lipids and Proteins Analytical Department, we are looking for a highly motivated Senior Scientist to join us in working with analytical instrumentation, especially with LC-High Resolution Mass Spectrometry, LC-MS/MS methodology for global profiling of synthetic materials, impurities, lipids and metabolic biomarkers. This role would suit a successful Scientist that has experience with LC-MS/MS method development, is familiar with building Lipid data bases and analysis of lipid pathways, and possesses a BS w-6 years of experience, or a MS w-3 years of experience —  and/or a PhD. Yoh is in a unique position, we have to find the best technical talent, provide services to some of the world’s largest companies, and be a great employer. We do that with the great people we have working for us. This Senior Scientist opportunity is with our client in Cambridge, MA. The role is for a direct-hire opportunity with a competitive salary and benefits package, relocation assistance, H1B sponsorship eligibility, and a monthly transportation stipend, as well as yearly performance incentives. This client is globally recognized as a leader in providing analytical testing services to clients across multiple industries both nationally and internationally.  We strive to be a company that embraces diversity, is inclusive, and thrives on learning so that our employees feel respected and invited to contribute to the success of our company, clients, suppliers, and communities.Your ContributionEssential FunctionsThis position will provide support for the Metabolomics/Metabolic biomarkers/Proteomics for Early Development by developing LC-High Resolution MS methods for global profiling of synthetic materials, impurities, lipids and metabolic biomarkers.Your AccomplishmentsRequired SkillsB.S. 5+ years of related experience; M.S. 3-7 years of related experience; PhD with related experience.LC-High Resolution MS method development for global profiling of synthetic materials, impurities, lipids and metabolic biomarkersWorking with analytical instrumentation, especially with LC – High Resolution Mass spectrometry (preferably Orbitrap MS) and Triple quadrupole Mass spectrometers (preferably SciEx)Maintenance, cleaning, tuning and troubleshooting of the mass spectrometersDevelopment and implementation of LC-MS methods, for characterization and quantitative analysisSample preparation, including biological and synthetic samplesLipidomic and Metabolomic analysesProcessing of High-Resolution MS data, building and using data bases and programming skillsYour Benefits & CompensationCompensation $100,000-$118,000, Depending on experienceDirect Hire Opportunity! Sponsorship for 2024 Eligibility!BenefitsRelocation StipendMonthly Transportation Stipend  Medical, Dental & Vision Benefits401K Retirement Saving PlanLife & Disability InsurancePerformance Incentives Opportunity is Calling, Apply Now! | Recruiter: Amber Meza, Amber.Meza@yoh.com   Yoh makes finding and applying for jobs simple. Partner with Yoh to find the right opportunities across multiple industries in the US and UK. Find out more here.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 https://www.yoh.com/applicants-with-disabilities to contact us if you are an individual with a disability and require accommodation in the application process.

Full Time
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Scientist II
Novo Nordisk
location-iconLexington MA

About the DepartmentDicerna, a Novo Nordisk company, is focused on driving innovation in RNAi (ribonucleic acid interference) to selectively target and silence genes that cause or contribute to disease. Our proprietary GalXC™ and GalXC-Plus™ RNAi technologies have the potential to address conditions that are difficult or impossible to treat with other modalities. Established as a Transformational Research Unit (TRU) following Novo Nordisk’s acquisition of Dicerna Pharmaceuticals, Inc. in December 2021, the Dicerna TRU is a unique new organization within Novo Nordisk that brings together the best of both worlds – the agility, collaborative pioneering spirit and calculated risk-taking profile of a biotech along with the scale, resources and capabilities of a global leader in drug development. With approximately 200 researchers, scientists, drug developers and operational staff, we are a team of inventive and entrepreneurial thinkers pushing the boundaries of science to create and drive new RNAi-based therapies for both rare and more prevalent diseases from the bench to the clinic. Together, we are driving change. Are you ready to make a difference?The PositionWe are currently seeking a highly skilled and motivated synthetic chemist ready to function in a fast-paced and collaborative environment. The successful candidate will be part of the chemistry group responsible for the synthesis of nucleoside analogues, small molecule ligands, linkers, and oligonucleotide conjugates and will work closely with contract research/manufacturing organizations on the scale-up and tech transfer of the processes.RelationshipsThis role will report to a senior director in Medicinal Chemistry.Essential FunctionsDesign, plan and execute multi-step organic synthesis and purification of high quality target moleculesReview research papers and intellectual property literature and propose novel target moleculesOperate and maintain multiple instrumentation including HPLC, LCMS for purification, characterization and purity determination of prepared compoundsLeading from the bench, oversee the efforts of external and/or internal chemists to troubleshoot organic chemistry experiments to reach desired goalsAssist in the planning and management of external research efforts for contract research organizations and collaborationsFunction as a senior member of the chemistry group aiding in the preparation of intellectual property, publications, and project planningPhysical Requirements0-10% overnight travel required. Ability to lift 0-10 lbs.QualificationsPh.D. in organic chemistry with 1+ years of relevant experienceIn-depth knowledge of organic chemistry reactions and mechanismsExperience with chromatography techniques i.e. LC-MS, ion exchange and RP-HPLCThorough understanding of analytical techniques (HPLC, LC-MS, etc) for characterization of prepared compoundsThe successful candidate must be a resourceful and proactive individual who is able to work as a team player in a dynamic environment with tight deadlinesDemonstrate clear alignment with Dicerna Core Values including, Dedication, Innovation, Communication, Excellence, Respect, Need Based, and AccountabilityPreferred Qualifications:Experience in heterocyclic and/or carbohydrate chemistry, familiarity with nucleoside synthesis, bio conjugate chemistry is a plusKnowledge in oligonucleotide chemistryWe commit to an inclusive recruitment process and equality of opportunity for all our job applicants.At Novo Nordisk we recognize that it is no longer good enough to aspire to be the best company in the world. We need to aspire to be the best company for the world and we know that this is only possible with talented employees with diverse perspectives, backgrounds and cultures. We are therefore committed to creating an inclusive culture that celebrates the diversity of our employees, the patients we serve and communities we operate in. Together, we’re life changing.Novo Nordisk is an equal opportunity employer. Qualified applicants will receive consideration for employment without regard to race, ethnicity, color, religion, sex, gender identity, sexual orientation, national origin, disability, protected veteran status or any other characteristic protected by local, state or federal laws, rules or regulations.Novo Nordisk requires all new hires to be fully vaccinated against COVID-19 prior to the first date of employment. As required by applicable law, Novo Nordisk will consider requests for reasonable accommodation.If you are interested in applying to Novo Nordisk and need special assistance or an accommodation to apply, please call us at 1-855-411-5290. This contact is for accommodation requests only and cannot be used to inquire about the status of applications.

Full Time
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React/C#/.NET/Azure Senior Software Engineer
Motion Recruitment
location-iconBoston MA

Job Description A company in the greater Boston area is looking for a short-term contractor to join their team either on a hybrid model or fully remote. They are an investment management company that works with several high-profile tech companies in the area. They are targeting somebody skilled in React, C#, .NET Core, and SQL. They are looking to update two of their crucial business applications into React and .NET Core. The first is an application used by their internal employees as a database to close future investments and the other is used to provide information on who to contact. Contract Duration: 3 – 6 Months Required Skills & Experience Highly skilled in C# and .NET development Skilled in React Exposure to cloud, Azure preferred, open to AWS and GCP Desired Skills & Experience 5+ years of experience Previous experience in the investment space BS/MS in Computer Science or Related Field What You Will Be Doing Daily Responsibilities: 100% Hands On #LI-JD7

Full Time
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Research Associate/Sr Research Associate- Biotransformation
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 DescriptionOBJECTIVES:Research Associate/Sr Research Associate: Metabolite ID/Catabolite ID/Biotransformation, DMPK, Takeda Pharmaceutical Company, Cambridge, MAThe DMPK department at Takeda, Cambridge, MA is seeking a highly motivated Research Associate or Sr Research Associate to join the Drug Metabolism group. The primary responsibilities will be profiling and characterization of metabolites (small molecules, ASO, and siRNA )/catabolites (ADCs, proteins, and 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.ACCOUNTABILITIES:1. Identification and structural elucidation of metabolites/catabolites of small molecule, ASO, siRNA, ADC, peptide, and protein drug candidates using LC-MS and other structure elucidation tools.2. Hands on experience in operation, maintenance & trouble shooting of LC-MS, immune-capturing technology, and other instruments.3. Conduct in vitro drug metabolism studies of small molecules, payload release assays of ADCs, catabolism and stability assessment of peptide and protein drugs.4. Conduct non-radio-labeled and radio-labeled metabolite profiling experiments from in vitro and in vivo studies (pre-clinical and clinical mass balance studies).5. Work independently or under guidance and report data in written reports and team presentations as required.6. Maintain accurate records of the study data.EDUCATION, BEHAVIOURAL COMPETENCIES AND SKILLS: Applicants should possess a MS or BS in Organic/Analytical/Medicinal/Bio chemistry or relevant discipline with 0 year (MS) or 2+ years (BS) of pharmaceutical industry experience. Hands-on experience with HPLC and LC-MS are preferred. Familiarity with 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 metabolism Experience in utilizing radiolabeled material in drug metabolism studies is a plus. Experience in immunocapture and protein/peptide qualitative analysis by LC-MS is a plus. Experience in metabolism of new modalities (e.g. ASO, siRNA) is a plus. Experience in metabolite/catabolite identification in in vitro systems (hepatocytes, microsome, etc.) and 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.Employees are eligible to participate in Medical, Dental. Vision, Life Insurance, 401(k), Charitable Contribution Match, Company Holidays, Personal & Vacation Days, Student Loan Repayment Program and Paid Volunteer Time Off.Effective November 1, 2021, absent an approved religious or medical reason, all US office-based and lab-based Takeda employees who work fully on-site or in a hybrid model (as determined by Takeda) must be fully vaccinated to work at a Takeda site or to engage with Takeda colleagues or anyone else on behalf of Takeda. As of the same date, absent an approved religious or medical reason, US field-based employees, employees must be fully vaccinated in order to continue in their current roles. US employees who work at a Takeda manufacturing facility, and those who work at a BioLife center or BioLife lab, may be subject to different guidelines. Candidates are encouraged to speak with their recruiter to seek further information on the applicable guidelines for the Business Unit/Function for which they have applied.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

Full Time
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Software Engineer Angular.js/ASP.NET/C#/SQL
Motion Recruitment
location-iconBoston MA

A Logistics and supply chain SaaS company in the greater Boston area is looking for a Software Developer to join their core team. This is a Contract to Hire opportunity targeting a 6 month long contract. They are looking for an individual to go into the office on a hybrid basis. The ideal candidate has a few years of experience under their belt and is skilled in Angular.js, C#, ASP.NET, and SQL. This SaaS company creates a comprehensive parcel management application, acting as a substitute for Amazon. They handle all the management of connecting the provider with the best mail company. Their products keep tabs on delivery times and accessibility, so the client is getting the quickest service possible. Contract Duration: 6 Months Required Skills & Experience Experience developing in C#, and ASP.NET Core Skilled in Angular.js Strong development experience using SQL BS or MS in computer science, related field, or equivalent work experience Desired Skills & Experience Exposure to Cloud, Azure, AWS, or GCP Skilled in Angular 2+ Past experience in the Logistics and Supply Chain What You Will Be Doing Daily Responsibilities 100% Hands On #LI-JD7

Full Time
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Research Associate, LC, LC/MS
Toxikon Corporation
location-iconBedford MA

Research Associate, LC, LC/MSToxikon Corporation, originally founded in 1977, is a Contract Research and testing company with laboratories in Bedford, MA. Our mission continues to focus on providing quality services, competitively priced, with on-time delivery for the Pharmaceutical, Medical Device and Biotech industries.As a Research Associate for our Analytical Dept., candidates will be responsible for providing technical expertise in supporting preclinical studies conducted under GLP, ISO 17025, and various other regulatory agencies. Research Associates 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 maintenanceExperience 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 suppliesReview 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 standardsExperience with other analytical instrumentation including, GC/FID, GC/MS, and TOC preferredEducation:Bachelor’s degree in Chemistry, with preferably 3-5 years of equivalent laboratory experience. However, we are willing to train the right candidate. Must have some knowledge of GMP/GLP regulations in an analytical laboratory setting, exceptional oral and written communication skills, and ability to work in a high volume, fast paced environment.Toxikon offers a comprehensive benefits program including: paid vacation, sick and personal time, 401(k) plan with company match, medical, dental, vision care, life insurance, short and long-term disability insurances, flexible spending accounts, employee assistance program, employee referral bonus, discount programs and more.Toxikon is an equal opportunity employer. As an equal opportunity employer we do not unlawfully discriminate against any applicant because of race, sex, gender, ethnicity, religion, creed, age, color, military/veteran status, genetic condition or information, Family and Medical Leave entitlement, sexual orientation, gender identity, national origin, ancestry, marital status, qualified physical or mental disability, transgender status, or any other legally

Full Time
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Senior Program Manager, Preclinical - Biotech - Boston
Michael Page
location-iconWaltham MA

* Support R&D management with the development of integrated development program plans containing current and future asset strategies * Establish execution strategies for operational objectives, deliverables, and timelines * Partner with R&D Project Leads to progress the portfolio * Work collaboratively with Global cross-functional project teams and early clinical development leadership * Lead Program activities from lead optimization to IND-filling * Work with external contract organizations (CROs/CMOs) and establish project plans to drive the delivery of project milestones to meet budget and time-lines * Monitor projects for potential risks and develop strategies to mitigate future risks * Effectively communicate across teams and provide CROs CMOs with regular ad-hoc status updates MPI does not discriminate on the basis of race, color, religion, sex, sexual orientation, gender identity or expression, national origin, age, disability, veteran status, marital status, or based on an individual's status in any group or class protected by applicable federal, state or local law. MPI encourages applications from minorities, women, the disabled, protected veterans and all other qualified applicants. * B.S. in scientific discipline with 10+ years of R&D experience in Pharma/Biotech Industry, specifically in drug discovery and development * Higher degree or certification (M.S., MBA, PMP, etc...) is preferred but not required * 3+ years of direct Project Management experience in Biotech/Pharma industry * Experience with Immunology, Oncology, or biological therapeutics in pre-clinical development is preferred * Understanding of pre-clinical drug development processes * Experience with integrated timeline/Gantt chart development * Technical experience with PM Systems and tools (MS Projects, OnePager, MS Teams, Sharepoint, etc...) * Excellent written and verbal communications skills * Ability to work in a fast-paced environment * Strong team building skills and able to develop effective teamwork between groups Our client is a Life Science company using multiple platforms across large and small molecules to develop novel therapeutics. They are in pre-clinical stages and advancing the development of immunotherapies for the treatment of cancer. This company has a European presence, and plans to grow its US headcount over the next year. * Competitive base salary and annual bonus * Stock options * Highly visible role throughout the organization * First Program Management hire for Pre-clinical Development * Hybrid work model * 401k * Great Health Benefits

Full Time
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Scientist I / RNA-based Therapeutics
Pioneer Data Systems Inc
location-iconCambridge MA

Our client, a world-leading Pharmaceutical Company in Cambridge, MA is currently looking for a Scientist I / RNA-based Therapeutics to join their expanding team. Position Details: Job Title: Scientist I / RNA-based Therapeutics Duration: 36 months contract Location: Cambridge, MA Note: The client has the right-to-hire you as a permanent employee at any time during or after the end of the contract. You may participate in the company group medical insurance plan Job Description: We are seeking a highly motivated contracting scientist to join the Molecular Assessment and Profiling group in BioMedicine Design at Pharmaceutical. The candidate will work with an innovative team of scientists to develop RNA-based therapeutics to bring curative treatments to patients. This individual will generate critical analytical characterization to support the RNA-based therapeutics development in discovery research and development using a suite of established methods (examples include qPCR, CGE and DLS). Job Requirements:Requirement: Detail oriented and organized; ability to complete experiments with limited supervision after trained Able to clearly communicate experiment results; experienced with using Microsoft PowerPoint and Excel for data presenting and reporting BA/BS with 2-3 years or MS with 0-1 years experience in molecular biology and/or biochemistry Preferred: Knowledgeable with RNA/DNA and lipids nanoparticle analytical characterization techniques including but not limited to qPCR, CGE (Tape Station/FA) and DLS size/PDI analysis Prefer candidate with RNA-based therapeutics or molecular biology emphasis Interview: 1st - Phone 2nd - WebEx (panel) Minimum Education: BA/BS with 2-3 years or MS with 0-1 years experience in molecular biology and/or biochemistry; Preferred candidate with RNA-based therapeutics or molecular biology emphasis

Full Time
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Senior Software Engineer- C#
Motion Recruitment
location-iconBoston MA

This multinational SaaS company provides clinical solutions pertaining to the life sciences industry. It is an integrated response software, that allows clinical study administrators to adaptively change parameters and tests in real time. They are looking for a Senior Software Engineer to join their headquarters in the North Boston area. The specific project you will be working on is developed for patient and site management, and drug supply management. Required Skills & Experience 4+ years of Software Development experience Experience with C#/.NET Experience with Javascript Frameworks (Angular, React, Vue) Desired Skills & Experience BS/MS Degree in computer science Experience with REST APIs Experience with SQL Offer You will additionally receive following benefits: Medical Insurance Dental Benefits Vision Benefits Paid Time Off (PTO) 401(k) Applicants must be currently authorized to work in the US on a full-time basis now and in the future #LI-DR4

Full Time
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Reporting Analyst
Experis
location-iconBoston MA

Experis, a ManpowerGroup company, has an exciting contract opportunity with one of our key clients, which is the leading financial services-based company in the US. It operates a brokerage firm, manages a large family of mutual funds, provides fund distribution and investment advice, retirement services, index funds, wealth management, cryptocurrency, securities execution and clearance, asset custody, and life insurance.Job Title: Reporting AnalystDuration: 6 Months (Possible Extension)Location: Boston MA 02109Job Description The position is critical to developing reporting and analysis to drive scale and efficiency across multiple systems, groups, and processes.We are looking for someone who is passionate about business intelligence, data visualization, business requirements exploration and discovery, systems improvements, data consumption processes and reporting.The ExpertiseThe ideal candidate will have 5-7+ years in the financial service industry, with experience using data and analytics to consult and inform strategy •Degree or experience in a quantitative analysis field (Engineering, Mathematics, Statistics, Finance or Business.) •Proficiency in Business Intelligence tools, analyzing large data sets, modeling, and presentation tools (MS Excel, MS PowerPoint) with experience in Tableau, Power BI etc. •Conceptual understanding of data collection and business Intelligence tools • Basic understanding of process improvement methodologies •Knowledge and experience with SQL and MS Excel •Strong analytical skills and problem-solving capabilities. •Good interpersonal skills, including excellent written and verbal communications skills •Learning mentality, always seek to understand the underlying technology working to effectively bridge between issues and their root cause •Ability to work on multiple assignments simultaneously •Strong team-oriented approach to getting work done The Value You Deliver •Providing analyses and strategic recommendations to team, management, and business partners • Synthesizing data, analyses, and conclusions into self-service dashboards or presentation format for senior management •Finding opportunities to streamline work processes to make the team more efficient and effective • Proactive partnership and communication with technology and operations business partners •Using tools and business knowledge to continuously provide insightful information, reporting and analytics that evolve with changes in the business How Your Work Impacts the Organization The Data and Reporting Analyst is responsible for the creation and monitoring of business operations, management and executive level reporting solutions that will help influence decision making and drive business processes. Special Instructions:Exp in data collection, data visulation and supporting an executive audience with visuals and analytics.Must have (Experience candidates must have coming in the door)? Must Need to have exp writing SQL code Must have Tableau development exp, create the dash and publish to server and maintain the code to tableau salesforce plus ad hoc basis, support other groups, good exposure, Multi-faceted support job.Apply Today

Full Time
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(Remote) Sr Director of Supply Chain - Biopharmaceuticals
Michael Page
location-iconWaltham MA

* Provide Supply Chain oversight for all cross-functional activities at the manufacturing sites and ensures contractual commitments are complied with by both parties. * Develop and oversee plans for commercial RSM, drug substance, drug product, and packaging that results in meeting commercial requirements. * Responsible for supplying drug product for all company sponsored clinical trials as well as all Investigator Sponsored Trials (IST's) * Establish and implement inventory policy and materials risk mitigation strategies * Develops and executes Supplier Governance Model at all CMO's to ensure appropriate controls and oversights are in place. * Responsible for managing Oracle ERP system database and compliance. * Works closely with CMC function to resolve any technical issues that arise at any CMO. * Partner with Quality assurance to ensure CMO's are in compliance with all cGMP guidelines and SOP requirements. * Support the financial planning processes (e.g., forecasting, strategic planning) by analyzing raw material and external supply partner requirements (e.g., Drug substance, drug product and packaging demand) on an annual basis and create material budget forecasts for strategic planning. MPI does not discriminate on the basis of race, color, religion, sex, sexual orientation, gender identity or expression, national origin, age, disability, veteran status, marital status, or based on an individual's status in any group or class protected by applicable federal, state or local law. MPI encourages applications from minorities, women, the disabled, protected veterans and all other qualified applicants. * BA/BS in Supply Chain/Operations or life sciences/health-related field. * Minimum of 12 years' experience in supply chain planning within the Pharmaceutical/Biotech industry. * Must have Supply Chain Management experience in commercial Biotech/Pharma. * Expertise in use of MS Excel, as well as demonstrated proficiencies in MS Project, Oracle ERP systems, and Visio. * Understanding of supply chain management and associated resources/tools, for both oral solid product and sterile vials with knowledge of contract manufacturing operations. * Must have the technical project management & external relationships experience necessary to lead the teams in a strategic and tactical manner * Able to prioritize multiple tasks from multiple parties and work in a fast-paced environment with tight deadlines. * Ability to travel up to 25% domestic and international travel along with the wiliness to attend various meetings at CMO sites This client is a rapidly growing biopharmaceutical start-up based in the Greater Boston area which has recently made a successful IPO, raised significant funding, and has commercialized its first drug/therapy to market. This company has several late-staged therapies within the oncology space and anticipates commercialization of its second drug over the next couple of years. * Impact role: Supply Chain Head role at the company, expected to own the function. * Remote position with travel. The team is willing to hire with expectations to travel to CMOs and visit onsite 3 days/month. * Competitive base salary. * Stock options. * Annual bonus. * Excellent benefits package. * Management opportunity - will take on 2 senior direct reports with opportunity to grow and hire. * Reports directly up to Senior leadership of a rapidly growing biotech start-up. * Successful IPO and strong financial health. * Novel drug portfolio with strong pipeline, including one therapy on market and second drug soon to follow.

Full Time
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Contracts Processor/Buyer Consultant
Gardner Resources Consulting, LLC
location-iconBoston MA

Our client is actively seeking a Contracts Processor/Buyer Consultant. This role assists in maintaining a portfolio of contracts and business relationships within the CFO organization as well as other procurement-related activities.Qualifications: 2+ years of experience in procurement and/or contract administration. Strong MS Office knowledge and experience working with ERP system(s) required; Oracle Fusion a plus. Knowledge of legal terminology and language related to supplier and/or vendor agreements and contracts. Demonstrated strong interpersonal skills; effective working collaboratively with cross-functional team members and external partners. BA/BS with a major in Business Management or Finance preferred. Experience within the pharmaceutical/life science industry is strongly preferred. Experience using a Contract Management System; Novatus is a plus. Excellent written and oral communication skills. Demonstrated ability and willingness to drill into operational details while maintaining an appropriate whole-company perspective (zoom-in, zoom-out). Strong analytical skills with superior attention to detail. Ability to manage multiple priorities with limited supervision. Experience working with all levels of management and consulting with key business stakeholders. An ability to influence for greater outcomes.

Full Time
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Title Researcher and Right of Way Specialist
share-icon
Full Time
location-iconBoston MA
Job Description

Title Researcher / Right-of-Way Specialist

Maverick Corporation is a full-service Engineering and Construction firm working in the telecommunications and electrical power sectors. Our customers range from traditional municipal and co-op electric utilities and telecommunication service providers to companies operating in the oil & gas and the transportation industries. Maverick Corporation and its affiliates provide project management, quality control and review services; aerial, underground, and technical services in construction; as well as design, survey, permitting, and owner's agent services in engineering. Maverick has been incorporated since 1994, and is a growing company with headquarters in Boston, Massachusetts.

Maverick is seeking a Title Researcher/Right of Way Specialist to support our growing engineering team headquartered in Boston, MA with offices across the country. The ideal candidate will have experience working in the telecommunication, electrical engineering, and/or real estate fields. It shall require the ability to operate in a fast-paced environment assisting in researching and outlining requirements to successfully permit overhead and underground designs. This person will work closely with management for design, field, permitting, and GIS teams to establish a common understanding of the rights to land use and processes.

Responsibilities:

  • Identifies encroachment, trespass, and land use conflicts
  • Research title abstracts, deeds, and other data to determine boundaries and property rights
  • Performs rights assessments, identify record errors, gaps in rights, project permit needs
  • Coordinates work activities to support projects as assigned
  • Assisting in obtaining licenses, permits, or other as needed
  • Maintains and updates the Company's records/ database
  • Provides technical support and assistance to operating areas relative to ROW land management as assigned
  • Assists property right negotiations for the acquisition and disposition of property rights as assigned or directed
  • Performs vendor coordination as required
  • Responds to questions relating to land use codes by the client and project team
  • Maintain tracking spreadsheets as needed
  • Collaborate with project team to appropriate actions

Qualifications:

  • Associates or bachelor's degree in engineering, real estate, GIS, other related field, OR comparable professional experience
  • Experience with AutoCAD, ArcMap, and 3GIS or other mapping software is preferred
  • Proficient in MS Excel and/or similar spreadsheet applications
  • Creative and analytical mind with a willingness to learn
  • Must enjoy working in a fast paced, high-growth, and rapidly changing work environment
  • Highly flexible in daily duties and level of responsibility
  • Excellent oral and written communication skills
  • Previous utility engineering experience is a plus
  • Permitting or GIS experience is a plus
  • Successful completion of pre-employment drug & alcohol and background check requirements

Benefits

  • Ability to participate in the Company Health Care/ Dental / Vision programs
  • FSA/HSA plans available when you participate in Health Care plan
  • Ability to participate in the Long Term and Short-Term Disability Policy
  • Life Insurance covering one year's salary up to $100K
  • Ability to participate in Company 401K retirement account, Maverick will match up to 4% percent of your base pay
  • Salaried employees accrue 2 weeks paid time off each year




PI192192113

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Title Researcher and Right of Way Specialist
share-icon
Full Time
location-iconBoston MA
Job Description

Title Researcher / Right-of-Way Specialist

Maverick Corporation is a full-service Engineering and Construction firm working in the telecommunications and electrical power sectors. Our customers range from traditional municipal and co-op electric utilities and telecommunication service providers to companies operating in the oil & gas and the transportation industries. Maverick Corporation and its affiliates provide project management, quality control and review services; aerial, underground, and technical services in construction; as well as design, survey, permitting, and owner's agent services in engineering. Maverick has been incorporated since 1994, and is a growing company with headquarters in Boston, Massachusetts.

Maverick is seeking a Title Researcher/Right of Way Specialist to support our growing engineering team headquartered in Boston, MA with offices across the country. The ideal candidate will have experience working in the telecommunication, electrical engineering, and/or real estate fields. It shall require the ability to operate in a fast-paced environment assisting in researching and outlining requirements to successfully permit overhead and underground designs. This person will work closely with management for design, field, permitting, and GIS teams to establish a common understanding of the rights to land use and processes.

Responsibilities:

  • Identifies encroachment, trespass, and land use conflicts
  • Research title abstracts, deeds, and other data to determine boundaries and property rights
  • Performs rights assessments, identify record errors, gaps in rights, project permit needs
  • Coordinates work activities to support projects as assigned
  • Assisting in obtaining licenses, permits, or other as needed
  • Maintains and updates the Company's records/ database
  • Provides technical support and assistance to operating areas relative to ROW land management as assigned
  • Assists property right negotiations for the acquisition and disposition of property rights as assigned or directed
  • Performs vendor coordination as required
  • Responds to questions relating to land use codes by the client and project team
  • Maintain tracking spreadsheets as needed
  • Collaborate with project team to appropriate actions

Qualifications:

  • Associates or bachelor's degree in engineering, real estate, GIS, other related field, OR comparable professional experience
  • Experience with AutoCAD, ArcMap, and 3GIS or other mapping software is preferred
  • Proficient in MS Excel and/or similar spreadsheet applications
  • Creative and analytical mind with a willingness to learn
  • Must enjoy working in a fast paced, high-growth, and rapidly changing work environment
  • Highly flexible in daily duties and level of responsibility
  • Excellent oral and written communication skills
  • Previous utility engineering experience is a plus
  • Permitting or GIS experience is a plus
  • Successful completion of pre-employment drug & alcohol and background check requirements

Benefits

  • Ability to participate in the Company Health Care/ Dental / Vision programs
  • FSA/HSA plans available when you participate in Health Care plan
  • Ability to participate in the Long Term and Short-Term Disability Policy
  • Life Insurance covering one year's salary up to $100K
  • Ability to participate in Company 401K retirement account, Maverick will match up to 4% percent of your base pay
  • Salaried employees accrue 2 weeks paid time off each year




PI192192113