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Viral Vector - Upstream Pilot
Takeda Pharmaceutical
location-iconWinthrop 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 DescriptionAt Takeda, we are a forward-looking, world-class R&D organization that unlocks innovation and delivers transformative therapies to patients. By focusing R&D efforts on four therapeutic areas and other targeted investments, we push the boundaries of what is possible in order to bring life-changing therapies to patients worldwide.Join Takeda as a Viral Vector - Upstream Pilot where you will be an important member within a small group responsible for owning and performing non-GMP Pilot upstream cell culture operations within a viral vector lab supporting both cell and gene therapy groups. You will also lead vial thaw, expansion, and production of both adherent cultures in cultures in flask/stack operation and suspension cultures, harvest, and filtration of batches to support development and clinical timelines. As part of the Viral Vector Pilot Operations and Scaleup Sciences, you will report to Associate Director CMC and work with upstream and downstream pilot team and with the process development and in-process analytics teams.How you will contribute:Cell culture (seed train/expansion/production bioreactor), harvest operations (filtrations or centrifugation), media/buffer planning and ordering, scheduling, large-scale column packing, sample forecasting and submission, metabolite or sample measurement, assisting with assembly and disassembly of process equipment, authoring batch records/SOPs or proposing document revisions, and execution of these records in both a cGMP and a non-GMP environment.Contribute to all technical operations within the Viral Vector Lab (VVL) for the upstream unit operations, both adherent and suspension, and process monitoring and data acquisition.Help create material supply campaign plans and coordination efforts with Cell and Gene therapy teams to meet timeline and quantity demands.Participate in most aspects of tech transfer from non-GMP Pilot team of cell culture process for biologics production into cGMP manufacturing stage.Document data in laboratory notebooks and batch records completely following established company guidelines/SOPs. Write documents such as reports, protocols and internal presentations that may require substantial edits.Help lead studies and technology evaluations that lead to IP, publications, external abstracts and presentations at industry events and conferences.Organize and present issues and results at departmental and project meetings.Interpret data and contribute to technical reports.Contribute to the design of new applications/experiments/unit operations in consultation with manager.Support technology transfer through writing and consolidating technical documents.Contribute to the non-GMP upstream efforts and responsible for independently preparing and executing routine and complex experiments and unit operations.Plan unit operations and experiments drafting support documentation (SOPs, batch records, and/or reports).Collaborate within the framework of cross-functional process development teams including engineers and manufacturing teams.Lift, pull or push equipment requiring up to 25-75 lbs of force.Minimum Requirements/Qualifications:Associate degree in chemical engineering, biotechnology, chemistry, biology, pharmacy, engineering, or related pharmaceutical science and 4+ years relevant industry experience.Bachelor's degree in chemical engineering, biotechnology, chemistry, biology, pharmacy, engineering, or related pharmaceutical science; 2+ years relevant industry experience.Master's degree in chemical engineering, biotechnology, chemistry, biology, pharmacy, engineering, or related pharmaceutical science; 0+ years relevant industry experience.Previous experience working in manufacturing or lab setting or master's degree plus appropriate laboratory training.Experience with cell culture is required with purification experience also desired, as this role will support both upstream and downstream operations.Experience with cell culture and aseptic techniques.Experience with laboratory equipment that supports cell culture, such as bioreactors and/or adherent culture stacks, metabolite analyzers, shake flasks, cell culture plates.Experience using automation preferred.Experience with electronic batch record system preferred.Experience with chromatographic and other protein separation principles.Familiarity with use of bio-separation equipment and standard analytical assays.You must be customer-focused, results oriented, science-driven, and have high attention to detail.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.#LI-SB1EEO 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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mRNA Pilot Plant- Team Lead
Yoh
location-iconWaltham MA

Primary Duties: Yoh has a Long Term Opportunity for an mRNA Pilot Plant Team Lead needed with Yoh Scientific's client located in Waltham, MA. This position is in the mRNA Process Development Group of a major pharmaceutical company, and requires a Bachelor's of Science degree and 5+ years of experience in a laboratory testing environment. Schedule is full-time M-F (7am-8am start time, 8 hour shift) and may require flexibility to work some evenings and overtime due to projects.   Responsibilities include but are not limited to:The mRNA Pilot Plant Team Lead supports the Process Development group in Waltham, MA, and reports to Yoh Management.We are seeking an individual to lead an mRNA GPH&TT team with pilot scale manufacturing skills and experience.Working hands-on to produce large-scale mRNA and LNP batches.Leading and completing large-scale buffer preparation.Leading and cleaning, setting up, and sanitizing large-scale process equipment.Documenting process equipment and operating parameters using an electronic notebook.Setting up and testing new equipment.Compiling data in spreadsheets.  Education and Experience Requirements:Minimum bachelor's degree or MS.5+ years of experience in laboratory.Hands-on experience with mixing, depth filtration, and TFF preferred.Desire to work in a fast-paced environment.Organizational and communication skills.Ability to be flexible and responsive to change, be a results-driven problem solver.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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Viral Vector - Upstream Pilot
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 DescriptionAt Takeda, we are a forward-looking, world-class R&D organization that unlocks innovation and delivers transformative therapies to patients. By focusing R&D efforts on four therapeutic areas and other targeted investments, we push the boundaries of what is possible in order to bring life-changing therapies to patients worldwide.Join Takeda as a Viral Vector - Upstream Pilot where you will be an important member within a small group responsible for owning and performing non-GMP Pilot upstream cell culture operations within a viral vector lab supporting both cell and gene therapy groups. You will also lead vial thaw, expansion, and production of both adherent cultures in cultures in flask/stack operation and suspension cultures, harvest, and filtration of batches to support development and clinical timelines. As part of the Viral Vector Pilot Operations and Scaleup Sciences, you will report to Associate Director CMC and work with upstream and downstream pilot team and with the process development and in-process analytics teams.How you will contribute:Cell culture (seed train/expansion/production bioreactor), harvest operations (filtrations or centrifugation), media/buffer planning and ordering, scheduling, large-scale column packing, sample forecasting and submission, metabolite or sample measurement, assisting with assembly and disassembly of process equipment, authoring batch records/SOPs or proposing document revisions, and execution of these records in both a cGMP and a non-GMP environment.Contribute to all technical operations within the Viral Vector Lab (VVL) for the upstream unit operations, both adherent and suspension, and process monitoring and data acquisition.Help create material supply campaign plans and coordination efforts with Cell and Gene therapy teams to meet timeline and quantity demands.Participate in most aspects of tech transfer from non-GMP Pilot team of cell culture process for biologics production into cGMP manufacturing stage.Document data in laboratory notebooks and batch records completely following established company guidelines/SOPs. Write documents such as reports, protocols and internal presentations that may require substantial edits.Help lead studies and technology evaluations that lead to IP, publications, external abstracts and presentations at industry events and conferences.Organize and present issues and results at departmental and project meetings.Interpret data and contribute to technical reports.Contribute to the design of new applications/experiments/unit operations in consultation with manager.Support technology transfer through writing and consolidating technical documents.Contribute to the non-GMP upstream efforts and responsible for independently preparing and executing routine and complex experiments and unit operations.Plan unit operations and experiments drafting support documentation (SOPs, batch records, and/or reports).Collaborate within the framework of cross-functional process development teams including engineers and manufacturing teams.Lift, pull or push equipment requiring up to 25-75 lbs of force.Minimum Requirements/Qualifications:Associate degree in chemical engineering, biotechnology, chemistry, biology, pharmacy, engineering, or related pharmaceutical science and 4+ years relevant industry experience.Bachelor's degree in chemical engineering, biotechnology, chemistry, biology, pharmacy, engineering, or related pharmaceutical science; 2+ years relevant industry experience.Master's degree in chemical engineering, biotechnology, chemistry, biology, pharmacy, engineering, or related pharmaceutical science; 0+ years relevant industry experience.Previous experience working in manufacturing or lab setting or master's degree plus appropriate laboratory training.Experience with cell culture is required with purification experience also desired, as this role will support both upstream and downstream operations.Experience with cell culture and aseptic techniques.Experience with laboratory equipment that supports cell culture, such as bioreactors and/or adherent culture stacks, metabolite analyzers, shake flasks, cell culture plates.Experience using automation preferred.Experience with electronic batch record system preferred.Experience with chromatographic and other protein separation principles.Familiarity with use of bio-separation equipment and standard analytical assays.You must be customer-focused, results oriented, science-driven, and have high attention to detail.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.#LI-SB1EEO 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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Viral Vector - Upstream Pilot
Takeda Pharmaceutical
location-iconBrookline Village 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 DescriptionAt Takeda, we are a forward-looking, world-class R&D organization that unlocks innovation and delivers transformative therapies to patients. By focusing R&D efforts on four therapeutic areas and other targeted investments, we push the boundaries of what is possible in order to bring life-changing therapies to patients worldwide.Join Takeda as a Viral Vector - Upstream Pilot where you will be an important member within a small group responsible for owning and performing non-GMP Pilot upstream cell culture operations within a viral vector lab supporting both cell and gene therapy groups. You will also lead vial thaw, expansion, and production of both adherent cultures in cultures in flask/stack operation and suspension cultures, harvest, and filtration of batches to support development and clinical timelines. As part of the Viral Vector Pilot Operations and Scaleup Sciences, you will report to Associate Director CMC and work with upstream and downstream pilot team and with the process development and in-process analytics teams.How you will contribute:Cell culture (seed train/expansion/production bioreactor), harvest operations (filtrations or centrifugation), media/buffer planning and ordering, scheduling, large-scale column packing, sample forecasting and submission, metabolite or sample measurement, assisting with assembly and disassembly of process equipment, authoring batch records/SOPs or proposing document revisions, and execution of these records in both a cGMP and a non-GMP environment.Contribute to all technical operations within the Viral Vector Lab (VVL) for the upstream unit operations, both adherent and suspension, and process monitoring and data acquisition.Help create material supply campaign plans and coordination efforts with Cell and Gene therapy teams to meet timeline and quantity demands.Participate in most aspects of tech transfer from non-GMP Pilot team of cell culture process for biologics production into cGMP manufacturing stage.Document data in laboratory notebooks and batch records completely following established company guidelines/SOPs. Write documents such as reports, protocols and internal presentations that may require substantial edits.Help lead studies and technology evaluations that lead to IP, publications, external abstracts and presentations at industry events and conferences.Organize and present issues and results at departmental and project meetings.Interpret data and contribute to technical reports.Contribute to the design of new applications/experiments/unit operations in consultation with manager.Support technology transfer through writing and consolidating technical documents.Contribute to the non-GMP upstream efforts and responsible for independently preparing and executing routine and complex experiments and unit operations.Plan unit operations and experiments drafting support documentation (SOPs, batch records, and/or reports).Collaborate within the framework of cross-functional process development teams including engineers and manufacturing teams.Lift, pull or push equipment requiring up to 25-75 lbs of force.Minimum Requirements/Qualifications:Associate degree in chemical engineering, biotechnology, chemistry, biology, pharmacy, engineering, or related pharmaceutical science and 4+ years relevant industry experience.Bachelor's degree in chemical engineering, biotechnology, chemistry, biology, pharmacy, engineering, or related pharmaceutical science; 2+ years relevant industry experience.Master's degree in chemical engineering, biotechnology, chemistry, biology, pharmacy, engineering, or related pharmaceutical science; 0+ years relevant industry experience.Previous experience working in manufacturing or lab setting or master's degree plus appropriate laboratory training.Experience with cell culture is required with purification experience also desired, as this role will support both upstream and downstream operations.Experience with cell culture and aseptic techniques.Experience with laboratory equipment that supports cell culture, such as bioreactors and/or adherent culture stacks, metabolite analyzers, shake flasks, cell culture plates.Experience using automation preferred.Experience with electronic batch record system preferred.Experience with chromatographic and other protein separation principles.Familiarity with use of bio-separation equipment and standard analytical assays.You must be customer-focused, results oriented, science-driven, and have high attention to detail.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.#LI-SB1EEO 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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mRNA Pilot Plant- Team Associate II
Yoh
location-iconWaltham MA

mRNA Pilot Plant Team Associate II   Primary Duties: Yoh has a Long Term Opportunity for an mRNA Pilot Plant Team Associate II needed with Yoh Scientific's client located in Waltham, MA. This position is in the mRNA Process Development Group of a major pharmaceutical company, and requires a Bachelor's of Science degree. Schedule is full-time M-F (7am-8am start time, 8 hour shift) and may require flexibility to work some evenings and overtime due to projects.   Responsibilities include but are not limited to:The mRNA Pilot Plant Team Associate II supports the Process Development group in Waltham, MA, and reports to Yoh Management.We are seeking an individual to assist an mRNA GPH&TT team with pilot scale manufacturing skills and experience.Working hands-on to produce large-scale mRNA and LNP batches.Completing large-scale buffer preparation.Cleaning, setting up, and sanitizing large-scale process equipment.Documenting process equipment and operating parameters using an electronic notebook.Setting up and testing new equipment.Compiling data in spreadsheets.  Education and Experience Requirements:Minimum bachelor's degree or MS.0+ years of experience in laboratory.Hands-on experience with mixing, depth filtration, and TFF preferred.Desire to work in a fast-paced environment.Organizational and communication skills.Ability to be flexible and responsive to change, be a results-driven problem solver. 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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Pilot in Command – Captain Citation X
Total Aviation Staffing, LLC
location-iconBoston MA

Job DescriptionOur client has taken a different approach to private jet travel. Their business model focuses on a local operation rather than a national operation. They are able to deliver unparalleled private jet benefits that result in an all-encompassing, local solution to all private jet travel needs.They are seeking self-motivated, safe, positive, enthusiastic, and goal-oriented individuals for an immediate opening as a Pilot in Command – Captain Citation X Midsize jet aircraft for Part 91 and 135 flight operations.Must reside within a 1-hour drive of commercial airport in these cities:Arlington, Atlanta, Austin, Baltimore, Bedford, Boston, Charlotte, Chicago, Dallas, Denver, Detroit, Dulles, Fort Lauderdale, Fort Myers, Fort Worth, Houston, Indianapolis, Kansas City, Miami, Minneapolis, Nashville, New Orleans, New York, Newark, Omaha, Orlando, Philadelphia, Phoenix, San Antonio, St. Louis, Teterboro, Tulsa.What Is In It For YouSalary: Competitive compensationPosition Type: Permanent - Full-timeBenefits:Medical, dental and vision insurance12 Duty Days and 23 nights at home on average per monthPTO with an additional floating holiday401k plan with a 100% company match up to 6% of the employee’s salaryCell phone stipendCompany-paid long-term and short-term disability coverageCompany-paid Life insuranceAnd many more amazing benefits!A Day In The Life of a Pilot in Command (PIC)As the Pilot in Command (PIC) you will report directly to the Base Chief Pilot. You will prepare and ensures the safe and efficient operation of company aircraft in accordance with the Federal Aviation Regulations and company procedures.Minimum RequirementsTotal Time - 3500 hoursTotal PIC - 2000 hoursTotal PIC Time in Type - 250 hoursTotal Multi-Engine - 2500 hoursTotal Multi-Engine PIC - 1500 hours​​​​​​Total Turbine - 2000 hoursMust Possess: ATPFCC Restricted Radio LicenseCurrent PassportFirst Class MedicalStrong Customer Service and Communication SkillsProactive decision-making skillsFlight activity within the last 24-monthsPreferred qualifications include:Initial or Recurrent 142 training in type within the last 24 months is also preferred.If you are interested in the Information Pilot in Command – Citation X job, apply today!​​This vacancy is being advertised by Total Aviation Staffing, LLC. The services advertised by Total Aviation Staffing, LLC are those of an Employment Agency

Full Time
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Pilot in Command – Captain Citation Sovereign
Total Aviation Staffing, LLC
location-iconBoston MA

Job DescriptionOur client has taken a different approach to private jet travel. Their business model focuses on a local operation rather than a national operation. They are able to deliver unparalleled private jet benefits that result in an all-encompassing, local solution to all private jet travel needs.They are seeking self-motivated, safe, positive, enthusiastic, and goal-oriented individuals for an immediate opening as a Pilot in Command – Captain Citation Sovereign Midsize jet aircraft for Part 91 and 135 flight operations.Must reside within a 1-hour drive of commercial airport in these cities:Arlington, Atlanta, Austin, Baltimore, Bedford, Boston, Charlotte, Chicago, Dallas, Denver, Detroit, Dulles, Fort Lauderdale, Fort Myers, Fort Worth, Houston, Indianapolis, Kansas City, Miami, Minneapolis, Nashville, New Orleans, New York, Newark, Omaha, Orlando, Philadelphia, Phoenix, San Antonio, St. Louis, Teterboro, Tulsa.What Is In It For YouSalary: Competitive compensationPosition Type: Permanent - Full-timeBenefits:Medical, dental and vision insurance12 Duty Days and 23 nights at home on average per monthPTO with an additional floating holiday401k plan with a 100% company match up to 6% of the employee’s salaryCell phone stipendCompany-paid long-term and short-term disability coverageCompany-paid Life insuranceAnd many more amazing benefits!A Day In The Life of a Pilot in Command (PIC)As the Pilot in Command (PIC) you will report directly to the Base Chief Pilot. You will prepare and ensures the safe and efficient operation of company aircraft in accordance with the Federal Aviation Regulations and company procedures.Minimum RequirementsTotal Time - 3500 hoursTotal PIC - 2000 hoursTotal PIC Time in Type - 250 hoursTotal Multi-Engine - 2500 hoursTotal Multi-Engine PIC - 1500 hours​​​​​​Total Turbine - 2000 hoursMust Possess: ATPFCC Restricted Radio LicenseCurrent PassportFirst Class MedicalStrong Customer Service and Communication SkillsProactive decision-making skillsFlight activity within the last 24-monthsPreferred qualifications include:Initial or Recurrent 142 training in type within the last 24 months is also preferred.If you are interested in the Information Pilot in Command – Citation Sovereign, apply today!​​This vacancy is being advertised by Total Aviation Staffing, LLC. The services advertised by Total Aviation Staffing, LLC are those of an Employment Agency

Full Time
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Pilot in Command – Captain Beechjet/Nextan
Total Aviation Staffing, LLC
location-iconBedford MA

Job DescriptionOur client has taken a different approach to private jet travel. Their business model focuses on a local operation rather than a national operation. They are able to deliver unparalleled private jet benefits that result in an all-encompassing, local solution to all private jet travel needs.They are seeking self-motivated, safe, positive, enthusiastic, and goal-oriented individuals for an immediate opening as a Pilot in Command – Captain Beechjet/Nextant Midsize jet aircraft for Part 91 and 135 flight operations.Must reside within a 1-hour drive of commercial airport in these cities:Arlington, Atlanta, Austin, Baltimore, Bedford, Boston, Charlotte, Chicago, Dallas, Denver, Detroit, Dulles, Fort Lauderdale, Fort Myers, Fort Worth, Houston, Indianapolis, Kansas City, Miami, Minneapolis, Nashville, New Orleans, New York, Newark, Omaha, Orlando, Philadelphia, Phoenix, San Antonio, St. Louis, Teterboro, Tulsa.What Is In It For YouSalary: Competitive compensationPosition Type: Permanent - Full-timeBonus: $10,000 sing on bonusBenefits:Medical, dental and vision insurance12 Duty Days and 23 nights at home on average per monthPTO with an additional floating holiday401k plan with a 100% company match up to 6% of the employee’s salaryCell phone stipendCompany-paid long-term and short-term disability coverageCompany-paid Life insuranceAnd many more amazing benefits!A Day In The Life of a Pilot in Command (PIC)As the Pilot in Command (PIC) you will report directly to the Base Chief Pilot. You will prepare and ensures the safe and efficient operation of company aircraft in accordance with the Federal Aviation Regulations and company procedures.Minimum RequirementsTotal Time - 3500 hours (4000 for 8/6 schedule position)Total PIC - 2000 hoursTotal PIC Time in Type - 250 hoursTotal Multi-Engine - 2500 hoursTotal Multi-Engine PIC - 1500 hours​​​​​​Total Turbine - 2000 hoursMust Possess: ATPFCC Restricted Radio LicenseCurrent PassportFirst Class MedicalStrong Customer Service and Communication SkillsProactive decision-making skillsFlight activity within the last 24-monthsPreferred qualifications include:Initial or Recurrent 142 training in type within the last 24 months is also preferred.If you are interested in the Information Pilot in Command – Pilot in Command – Captain Beechjet/Nextant job, apply today!​​This vacancy is being advertised by Total Aviation Staffing, LLC. The services advertised by Total Aviation Staffing, LLC are those of an Employment Agency

Full Time
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Pilot in Command - Captain Citation XLS/XLS
Total Aviation Staffing, LLC
location-iconBedford MA

Job DescriptionOur client has taken a different approach to private jet travel. Their business model focuses on a local operation rather than a national operation. They are able to deliver unparalleled private jet benefits that result in an all-encompassing, local solution to all private jet travel needs.They are seeking self-motivated, safe, positive, enthusiastic, and goal-oriented individuals for an immediate opening as a Pilot in Command – Citation XLS/XLS+ Midsize jet aircraft for Part 91 and 135 flight operations.Must reside within a 1-hour drive of commercial airport in these cities:Arlington, Atlanta, Austin, Baltimore, Bedford, Boston, Charlotte, Chicago, Dallas, Denver, Detroit, Dulles, Fort Lauderdale, Fort Myers, Fort Worth, Houston, Indianapolis, Kansas City, Miami, Minneapolis, Nashville, New Orleans, New York, Newark, Omaha, Orlando, Philadelphia, Phoenix, San Antonio, St. Louis, Teterboro, Tulsa.What Is In It For YouSalary: Competitive compensationPosition Type: Permanent - Full timeBonus: $10,000 Sign-on BonusBenefits:Medical, dental and vision insurance12 Duty Days and 23 nights at home on average per monthPTO with an additional floating holiday401k plan with a 100% company match up to 6% of the employee’s salaryCell phone stipendCompany-paid long-term and short-term disability coverageCompany-paid Life insuranceAnd many more amazing benefits!A Day In The Life of a Pilot in Command (PIC)As the Pilot in Command (PIC) you will report directly to the Base Chief Pilot. You will prepare and ensures the safe and efficient operation of company aircraft in accordance with the Federal Aviation Regulations and company procedures.Minimum RequirementsTotal Time - 3500 hoursTotal PIC - 2000 hoursTotal PIC Time in Type - 250 hoursTotal Multi-Engine - 1500 hoursTotal Multi-Engine PIC - 500 hours​​​​​​Total Turbine - 500 hoursStrong Customer Service and Communication SkillsProactive decision-making skillsPreferred qualifications include:Initial or Recurrent 142 training in type within the last 24 months is also preferred.If you are interested in the Information Pilot in Command – Citation XLS/XLS+ job in Houston, TX, apply today!​​This vacancy is being advertised by Total Aviation Staffing, LLC. The services advertised by Total Aviation Staffing, LLC are those of an Employment Agency

Full Time
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FW Pilot In Command
Boston MedFlight
location-iconBedford MA

Job DescriptionJOB SUMMARY: The Fixed Wing Pilot-in-Command position (PIC) is responsible for the safe and efficient conduct of a flight assignment. The PIC processes flight assignments received from MedFlight’s Communications Center and determines whether to accept or decline a flight assignment based on weather conditions or other factors that may impact the safety of flight. He/she will work collaboratively with the assigned second-in-command and other members of the medical flight team.ESSENTIAL DUTIES AND RESPONSIBILITIES:Under the immediate supervision of the Director of Aviation Operations and FW Chief Pilot, the PIC position:Performs Pilot-in-Command (PIC) duties for Boston MedFlight during flight assignments and serves as the team leader for all flight operations.Maintains responsibility for safe and efficient flight operations and is the final authority with regard to aircraft operations and flight safety. Plans flight assignments and obtains briefing information regarding purpose of the flight, weather, operating procedures and special instructions. Complies with all FAA Regulations, the General Operations Manual (GOM), safety management system (SMS) manual, training manual and all other Boston MedFlight policies and procedures. Conducts a start of shift briefing with the assigned medical, communications and ground personnel. Oversees SIC preparation of flight plans considering such factors as altitude, terrain, weather, range, weight, airport facilities and navigational aids. Utilizes the GOM in determining weather minimums to accept a flight assignment. Ensures at the beginning of the shift that the aircraft is pre-flighted per the GOM, inspected, loaded, equipped, fueled and staffed for a flight assignment. Completes a walk around inspection of the aircraft prior to initiation of every flight assignment. Supervises and assists loading and distribution of cargo and passengers and determines that weight and balance is within prescribed limitations per the utilized method of aircraft weight and balance or the approved flight manual. Ensures cargo is properly secured and emergency equipment is aboard. Assures flight plans are properly filed, activated and closed out.Checks aircraft maintenance log prior to flight to ensure all discrepancies have been corrected or properly deferred prior to a flight assignment.Assists in the loading and unloading of patients, as well as equipment decontamination in order to expedite the readiness status for subsequent transports.Logs all mechanical discrepancies as they occur and informs maintenance personnel. Immediately notifies the MedFlight Communications Center of any changes in the service status of the aircraft. Ensures proper completion of all required paperwork including flight logs, records and maintenance forms. Participates in debriefings on all flights. Competent in use of Electronic Flight Bag for navigation publicationsReports for duty on time for assigned shifts. Monitors all weather situations and updates the Communications Center of same. Notifies the Director of Operations or designee whenever the pilot may potentially violate any rule due to being dispatched on a flight. Notifies the Director of Operations whenever a personal medical deficiency exists that would affect the safety of flight. Maintains proficiency as Pilot-in-Command and proficiency in IFR operations. Attends multi-day Level D simulator proficiency flight training on an annual basis, or more frequently, as directed by the Chief Pilot. As operations permit, takes maximum advantage of time available in-flight to engage in training, such as practice instrument flight procedures, emergency procedures or crew discussion.Participates regularly in staff safety meetings, and public outreach duties that include Public Relations events, and other meetings as directed by the DO.The PIC may delegate functions to other personnel in the team but retains complete responsibility for safe flight operations.As operations permit, will assist aviation maintenance technicians in washing the aircraft and maintaining cleanliness of workspaces.Participates in the development, implementation, and evaluation of departmental aviation policies. Participates in an annual quality/performance improvement study, collateral duty, or project, as approved or assigned by the DO, which will directly address an issue to improve the safety, efficiency, or effectiveness of the aeromedical transport enterprise.Shares professional responsibility for identification, development and achievement of department goals. Promotes and maintains positive professional working relationships within the department and throughout the health system. Promotes the safety culture of Boston MedFlight and places safety as a top priority.Assists with operational demands by filling overtime shifts as required.Other duties as assigned by the Director of Aviation Operations and/or the Chief Pilot.Duties include occasional overnight assignments. Must report for duty prepared to remain overnight at the destination with minimal notice. Must be able to work varying hours including day and night, weekends, and holidays.Must be able to pass Transportation Security Administration required background screening, secure appropriate airport authority and / or Customs security badges.Must possess a Current Passport with unrestricted international travel privileges.Must possess a valid driver's license.SKILLS AND ABILITIES:Excellent written and verbal communication skills required.Ability to manage multiple deadlines and tasks.Demonstrates good decision-making skills.Demonstrates and promotes effective interpersonal skills. Demonstrates excellent organizational skills.Ability to develop presentations using Microsoft Office productsDemonstrates good public speaking skillsEDUCATION AND EXPERIENCE:3000 total flight hours preferred, with a minimum of 2,000 total flight hours required. 1,500 Pilot in Command hours, 500 hours multi-engine, 500 hours cross country, and 100 hours of night flight time all required. 1500 Hours turbine aircraft required.250 hours actual or simulated time required, including at least 50 hours in actual flight. 50 hours in actual IMC is desired. ATP license required or obtained within 1 year of employment. ATP – MEL certificate required, or obtained at pilot’s expense within 1 year of employment.FAA Class I Physical Medical Certificate.Preferred EMS experience within past 5 years. Citation Jet type rating with 25-hours in type, preferred.WORKING CONDITIONS/PHYSICAL REQUIREMENTS:Ability to operate aircraft and exposure to non-conventional motion, noise, vibration, jet fumes, cabin altitudes, and extreme temperatures.Ability to lift at least 50 pounds using proper body mechanics. Able to refuel aircraft at MedFlight bases and other sites. Able to pull fuel hoses in and out of the fuel trucks and fuel farm systems. Works in a patient care environment on the aircraft and is exposed to possible infectious diseases and chemical toxins. Follows all BMF infectious disease policies and protocols.Position may require sitting for long periods of time in a helicopter cockpit or in an office environment.BMF Class I employment physical required. Physical exams are performed by our occupational health provider or BMF contract AME.Height & weight requirement: In order to be eligible for employment, Body Mass Index (BMI) must not exceed 30 and/or the maximum weight for an individual crewmember must not exceed 210 pounds. Body fat percentage and frame size should be taken into consideration. Ability to assist in loading and unloading patients into MedFlight aircraft. Maintains a Class I Flight Physical. No physical restrictions wearing or donning Nomex flight suits, above the ankle leather boots, and night vision goggles in the helicopter environment. NOTES:An FBI background and CORI checks will be performed prior to employment. PRIA records or PRD check, pre-employment physical and drug/alcohol screen prior to hire. Full disclosure of any accidents, incidents, or prior regulatory action.Must pass random drug and alcohol screening in accordance with Part 120 of the Federal Aviation Regulations. FLSA Exempt The specific statements included in this job description are not intended to be all-inclusive but rather represent typical elements considered necessary to successfully perform the job.

Full Time
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Electronic Visit Verification System Specialist - Stoughton, Springfield or Danvers
Tempus Unlimited Inc.
location-iconStoughton MA

Description: Summary/Objective: Responsible for supporting Tempus Electronic Visit Verification (EVV) solution through pilot, implementation, and steady state environments. This involves a broad range of activities from testing through training and ongoing support, requiring developed project management and communication skills. Assure ongoing compliance with Tempus quality and FI contract requirements.Essential FunctionsDevelop and maintain expertise related to Tempus EVV solutionTest software, investigate issues and bugs, and dialogue with developers to ensure robustness of EVV solutionEngage in activities as directed to support full life cycle of Tempus EVV project. This includes but is not limited to:Pilot – coordination of users, review of data, multi-directional communicationImplementation/Roll-out – training, scheduling, support, multi-directional communicationOn-going support – troubleshooting, user support, enhancements definition Requirements: CompetenciesPhone experience and etiquette; inbound and outboundMicrosoft Office; Experience with Excel and spreadsheetsAbility to learn quickly and readily adapt to changeAbility to work independently while functioning effectively as a team memberWebEx experienceProject management experience in area of software user assessment testingWebsite work; how to maneuver through websitesEmpathy for callersSetup of apps on portal and download to phonesPatienceStrong written and oral communication skillsProfessional, friendly & understanding personalitySelf-motivationAbility to consistently maintain and build positive working relationshipsExcellent organizational skillsAbility to multi-task and meet deadlinesPunctuality and dependabilityFamiliarity with office machines, equipment and softwareAbility to respect and maintain confidentialityAttention to accuracy and detailStrong interpersonal and analytical skillsPreferred Experience: Proficiency in Microsoft Office softwareRequired Education: College Diploma or demonstrated work experienceWork Environment: This job operates in a professional office environment. This role routinely uses standard office equipment such as computers, phones, photocopiers, filing cabinets and fax machines.Physical DemandsThe physical demands described here are representative of those that must be met by an employee to successfully perform the essential functions of this job. While performing the duties of this job, the employee is regularly required to talk and/or hear. The employee is frequently required to sit; stand; walk; use hands to finger, handle or feel; and reach with hands and arms.Travel: Some in-state travel may be required for this position.Work Authorization/Security ClearanceAll offers of employment made by Tempus Unlimited are contingent upon satisfactory background check results. Pre-employment background checks will be conducted on all candidates that are offered a position at the agency in compliance with program policy as well as state and federal regulations. From time to time, these checks may be conducted on current employees to ensure compliance with all state and federal regulations and contracts.EEO StatementEqual Employment Opportunity is a fundamental principle at Tempus Unlimited where employment from recruiting through the end of employment is based upon professional capabilities and qualifications without discrimination because of race, color, religion, sex, age, sexual orientation, veteran status, national origin, disability or any other characteristic as established by law.Reasonable accommodations may be made to enable individuals with disabilities to perform the essential job functions.Other DutiesNote this job description is not designed to cover or contain a comprehensive listing of activities, duties or responsibilities that are required of the employee for this job. Duties, responsibilities and activities may change at any time with or without notice.PI192718942

Full Time
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Sr. Process Development Engineer-Reagents
Joule Staffing
location-iconBoston MA

Title: Sr. Process Development Engineer-Reagents Location: Boston MA Duration: Direct Hire Start: ASAP Schedule : Monday through Friday 8:00am to 4:30pm Experience - BS degree in a relevant Engineering discipline such as Biomedical, Chemical, Mechanical or equivalent required (MS degree in a relevant Engineering discipline Preferred but not required) - 3 yrs. exp. with reagent or chemical process equipment in the in-vitro diagnostics or pharmaceutical industry required - 3 yrs. exp. with medical device / IVD development under FDA Quality Systems Regulations, CE Marking, and ISO Quality Systems required - Strong hands-on skills with the ability to make routine mechanical and electrical repairs. Must be comfortable using basic tools and lab equipment - Knowledge of modern product development and project engineering principles, methods and practices Responsibilities: - Will be working with supply chain groups, vendors as well as develop/make cartridges, blood pumps and test products - Must own all technical aspects of this pilot line and be responsible for any repairs, maintenance and routine operation. This can include basic mechanical and electrical repairs as well as software and peripheral installation and maintenance - Will be solely responsible for the operation of a pilot production line for prototyping in-vitro diagnostic devices. They must be familiar with basic scientific processes such as reagent handling, pipetting, volumetric and gravimetric analytical techniques at the nanoliter level - This role will be responsible for the development and documentation of processes and procedures to ensure consistent and documented prototype production - This role must ensure consistent communication with the companies manufacturing facilities to confirm consistency between pilot line and production line processes. This will include any necessary travel - Analyzes experimental data, develops technical conclusions, and evaluates potential applicability of recommendations

Full Time
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Clinical Internal Medicine Physician
Brigham and Women's Physicians Organization
location-iconHingham MA

PRIMARY CARE PHYSICIAN Brigham and Women’s – HINGHAM, Scituate (South Shore, MA) Located on the South Shore, MA, Brigham and Women’s Primary Care as part of Harbor Medical Associates is seeking a Internal Medicine physician to join a thriving practice. Full or part-time FTE available.  BWH Primary Care provides comprehensive adult medical care for over 200,000 patients across our sixteen primary care practices throughout the greater Boston area. Our facilities are modern and patient-centered, with high-caliber clinical and support staff teams. Our PCPs see a complete range of adult patients across all demographics and diseases and conditions. Our growing network of primary care practices in eastern Massachusetts is testimony to Brigham and Women’s commitment to primary care as a critical component of managing populations, and our dedication to providing the best experience and health outcomes for our patients. We are searching for a board certified or eligible physician to join our friendly, busy and well-established practice. This position would see adults only. This physician group provides health screening, comprehensive diagnostic work-ups, treatment and long-term care. We offer: competitive salaries and benefit programs diverse primary care practice locations state-of-the-art EMR and enterprise data warehousing (in process) world-class integrated specialty network professional development programs NCQA PCHM recognized piloting innovative delivery models (e-visits, etc.) this is a non-teaching practice EEO Statement BWH is an Affirmative Action Employer. By embracing diverse skills, perspectives and ideas, we choose to lead.   We will ensure that all individuals with a disability are provided a reasonable accommodation to participate in the job application or interview process, to perform essential job functions, and to receive other benefits and privileges of employment.   Brigham and Women's Physicians Organization/Harvard Medical School is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability status, protected veteran status, or any other characteristic protected by law.

Full Time
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Sr. Process Development Engineer-Reagents
Joulé
location-iconBoston MA

Title: Sr. Process Development Engineer-Reagents Location:  Boston MA  Duration:  Direct Hire  Start: ASAP Schedule :  Monday through Friday 8:00am to 4:30pm  Experience - BS degree in a relevant Engineering discipline such as Biomedical, Chemical, Mechanical or equivalent required (MS degree in a relevant Engineering discipline Preferred but not required) - 3 yrs. exp. with reagent or chemical process equipment in the in-vitro diagnostics or pharmaceutical industry required - 3 yrs. exp. with medical device / IVD development under FDA Quality Systems Regulations, CE Marking, and ISO Quality Systems required - Strong hands-on skills with the ability to make routine mechanical and electrical repairs.  Must be comfortable using basic tools and lab equipment - Knowledge of modern product development and project engineering principles, methods and practices Responsibilities: - Will be working with supply chain groups, vendors as well as develop/make cartridges, blood pumps and test products - Must own all technical aspects of this pilot line and be responsible for any repairs, maintenance and routine operation.  This can include basic mechanical and electrical repairs as well as software and peripheral installation and maintenance - Will be solely responsible for the operation of a pilot production line for prototyping in-vitro diagnostic devices.  They must be familiar with basic scientific processes such as reagent handling, pipetting, volumetric and gravimetric analytical techniques at the nanoliter level - This role will be responsible for the development and documentation of processes and procedures to ensure consistent and documented prototype production - This role must ensure consistent communication with the companies manufacturing facilities to confirm consistency between pilot line and production line processes.  This will include any necessary travel - Analyzes experimental data, develops technical conclusions, and evaluates potential applicability of recommendations

Full Time
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Senior Level Process Engineer, Biologics - Biotech - MA
Michael Page
location-iconBoston MA

* Work with Pilot Plant Director, site functions, and project management to facilitate startup of the continuous pilot plant. Act as liaison between project manager and site functions to ensure completion of facility and start-up checklists and issue resolution. * Participate in site based cross-functional program teams as the representative of the continuous line that includes partnering with internal business and technical leadership and stakeholders, including site Manufacturing, Quality, and Facilities Engineering, as necessary to deliver project results in an efficient manner consistent with company's quality standards * Apply sound engineering theory and critical thinking to effectively resolve a variety of technical problems of moderate to large complexity and scope. * Participate in the development and use of data models for the model mAb process and other processes to be executed on the continuous manufacturing line * Monitor and trend process data to detect potential processing issues and to ensure effective process control. Employ statistical analysis and process modeling tools determine process performance, root cause for process anomalies, and deviations. Develop data analytic methods to extract process knowledge and understanding from process data. * Work with Process Development function, Suppliers, and Customers in a sandbox approach to test and implement new process technologies. * Support process investigations, equipment and process troubleshooting. * Implement process improvements using effective benefit and risk analysis supported by applying data analysis and effective planning. * Ensure safety and environmental measures are taken and appropriately addressed throughout the project. * Participate in Technology Transfer of scale-up, new process introductions, and client projects. 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. * BS or MSc in Engineering (Chemical, Biochemical), or relevant experience in a similar position in the sector of Biotech/Pharma with 7-10+ years' experience in process engineering or process sciences, or MS&T in a process development/pilot plant/cGMP manufacturing environment and unit operations such as Cell Culture, Chromatography, Filtration. * Abilities in process data analysis and modeling * Proven ability to prioritize and manage multiple projects and tasks * Experience in sourcing and using single-use disposable process elements and closed system operations * Project Engineering, preferably in a process development/GMP/biotech environment is a plus * Hands on experience in CMC manufacturing of biologic therapeutics specifically Monoclonal Antibodies and Recombinant Proteins is preferred. * Additional specific expertise in a field of biopharmaceutical industry (protein chemistry, regulatory, supply chain, production, etc.) is a plus Our client is a innovative and first-of-its-kind biopharmaceutical manufacturing company focusing on cell and gene therapies. They use cutting edge technology to increase efficiency and accuracy in the manufacturing process, all while maintaining capability to produce both modern and future therapies. These products are made quickly, safely and at scale due to the contiuous investment in R&D for next generation manufacturing and development. This company is growing at an exponential rate and establishing state-of-the-art facilities all around the country. * Extremely competitive compensation package * Annual bonus structure * New hire equity package * Full health benefits * 401k package * Free parking on site

Full Time
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Senior Process Development Engineer- Boston, MA
Michael Page
location-iconBoston MA

The Senior Process Development Engineer will be responsible for what follows: * Will be solely responsible for the operation of a pilot production line for prototyping in-vitro diagnostic devices. * Must own all technical aspects of this pilot line and be responsible for any repairs, maintenance and routine operation. * Development and documentation of processes to ensure consistent and documented prototype production. * Communicates risks and include their mitigations in the project planning activities. * Develops technical conclusions, analyzes experimental data and evaluates potential applicability of recommendations. * Coordinates work primarily across project team(s), related groups, or within the department. 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. The successful Senior Process Development Engineer will have SOME of what follows: * BS in a relevant Engineering discipline such as Biomedical, Chemical, Mechanical or equivalent required * 3 years experience with medical device / IVD development under FDA Quality Systems Regulations, CE Marking, and ISO Quality Systems required * Strong hands-on skills. Must be comfortable using basic tools and lab equipment * Outstanding communication skills and the ability to interact with a diverse cross-functional team. * Knowledge of modern product development and project engineering principles, methods This blood therapy medical device manufacturer started in Boston just over 40 years ago. The organization is targeting $990 million in revenue in 2022 and looking to exceed $1 billion in 2023. The fast growing team is expanding quickly in not only Massachusetts but across the entire country. The global business is publicly traded and is continuing to hit all time highs after the pandemic and as the demand of their product has launched them as the industry leader of blood and plasma therapy technology across the world. The successful Process Development Engineer will be offered: * Competitive Base Salary * Bonus Structure (can be paid up to 200%) * Clear growth trajectory * Lead in the beginning development of a new product * PTO, Health and 401k benefits * HYBRID WORK SCHEDULE * Cross functional with all department of the organization * Work along side the Senior Director in the beginning development

Full Time
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Naval Aviator
US Navy
location-iconBoston MA

About Search for underwater threats. Deliver payloads of incredible firepower or necessary manpower. Execute strategic aerial maneuvers anywhere from the stratosphere, to mere feet above the sea. This is just a glimpse into your career as a Naval Aviator. You also may find yourself: Flying some of the most innovative and high-tech aircraft in the world Providing vital attack, defense and logistic support to the Fleet Controlling and maintaining all internal and external aircraft systems Qualifications and Requirements A four-year degree is required to work as a Navy Pilot or Naval Flight Officer. Candidates seeking an Officer position in this community must have a bachelor's degree from a regionally accredited institution in a technical field. All candidates must also be U.S. citizens, willing to serve worldwide and qualified for sea duty. General qualifications may vary depending upon whether you're currently serving, whether you've served before or whether you've never served before. Learn more about life in the Navy at https://www.monster.com/company/profiles/US-NAVY-1

Full Time
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Senior Process Development Engineer- Boston, MA
Michael Page
location-iconBoston MA

The Process Development Engineer will develop a new product line through the Boston headquarters and be the face for the team as they grow out their team of development engineers. This candidate will work on design, development and new business ventures for one of the leading medical device organizations in the entire world. Client DetailsThis blood therapy medical device manufacturer started in Boston just over 40 years ago. The organization is targeting $990 million in revenue in 2022 and looking to exceed $1 billion in 2023. The fast growing team is expanding quickly in not only Massachusetts but across the entire country. The global business is publicly traded and is continuing to hit all time highs after the pandemic and as the demand of their product has launched them as the industry leader of blood and plasma therapy technology across the world.DescriptionThe Senior Process Development Engineer will be responsible for what follows: Will be solely responsible for the operation of a pilot production line for prototyping in-vitro diagnostic devices.Must own all technical aspects of this pilot line and be responsible for any repairs, maintenance and routine operation.Development and documentation of processes to ensure consistent and documented prototype production.Communicates risks and include their mitigations in the project planning activities.Develops technical conclusions, analyzes experimental data and evaluates potential applicability of recommendations.Coordinates work primarily across project team(s), related groups, or within the department. ProfileThe successful Senior Process Development Engineer will have SOME of what follows: BS in a relevant Engineering discipline such as Biomedical, Chemical, Mechanical or equivalent required3 years experience with medical device / IVD development under FDA Quality Systems Regulations, CE Marking, and ISO Quality Systems requiredStrong hands-on skills. Must be comfortable using basic tools and lab equipmentOutstanding communication skills and the ability to interact with a diverse cross-functional team.Knowledge of modern product development and project engineering principles, methodsJob Offer The successful Process Development Engineer will be offered: Competitive Base Salary Bonus Structure (can be paid up to 200%) Clear growth trajectory Lead in the beginning development of a new product PTO, Health and 401k benefits HYBRID WORK SCHEDULE Cross functional with all department of the organization Work along side the Senior Director in the beginning developmentMPI 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.

Full Time
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Solutions Engineer/Lead- Supply Chain SaaS
Michael Page
location-iconBoston MA

Job DescriptionThis role will be a player and eventual coach having the opportunity to build and scale an SE team. * Articulate benefits of complex technical solutions and products via industry and business terms to prospects and customers * Document and promote complete solutions via whiteboarding, pilots, and presentations * Partner with sales peers to drive new sales and expand existing business * Demonstrate understanding of the Transportation & Logistics market, including trends, industry business processes, and industry use cases * Maintain and apply knowledge of technical pre-sales, implementation of application integration & APIs * Deliver recommendations to product & engineering team members based on customer and prospective customer feedback * Execute customized product demonstrations that speak to the specific needs of the prospect * Run Value Assessments with prospective customers in order to produce a tailored and quantifiable ROI presentation * Coordinate with implementation team members to produce Statements of Work and technical design documents that fully capture project requirements * Support the response to RFP's, RFI's, and Information Security questionnaires * Engage with sales team members to run comprehensive discovery workshops with enterprise-level customers 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.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. The Successful Applicant*You Have:* * English + Spanish language would be a plus * Experience in pre-sales, implementation or consultative roles focused on SaaS technologies. Direct experience with Transportation, Logistics, Warehouse applications is strongly preferred. * Strong knowledge of global supply chain processes, including import/export management, ocean shipping, and freight forwarding. * Deep knowledge of logistics processes, including transportation management, warehousing, network design and maintenance, and inventory management * Proven track record of managing complex, technical sales cycles with global enterprises * Strong written and verbal communication skills, and ability to relay technical concepts to a non-technical audience. * Ability to understand and document technology requirements to integrate with cloud-based and on-premise applications * Experience with supporting web service integrations * High-level knowledge of application design principles and information security standards * Ability to troubleshoot and resolve technical issues in support of Proofs of Value and Pilots * Proficiency in SQL is a plus, but not required * Experience with field sales and willingness to travel up to 40% This recruitment assignment has been retained exclusively by Michael Page. Submit your resume today and Daniel LaBelle will review within 48 hours of submittal. If you are deemed suitable, you can expect a callback within 72 hours of submission. About Our ClientMy client is disrupting the Supply Chain / Logistics market with their SaaS solution. They are a series B funded, hypergrowth organization with high promise for IPO or acquisition. What's on Offer*Offer:* * Join a true rocket ship built for exit * $115k - 150k base + bonus (up to $225k OTE) * Benefits * Equity

Full Time
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Innovation Program Manager
Ivy Tech Solutions inc
location-iconBoston MA

Job DescriptionTitle: Innovation Program Manager – HC PM #141Location: 101 Huntington Avenue, Suite 1300, Boston, MA 02199Team: InnovationStart: 04/26/2021Interview Process: Phone/MS Teams video.- BCBSMA’s Well-B innovation function reporting to the Director of Innovation. Skip level is the Chief Innovation Officer. This is a high visibility role working on the largest transformation efforts within the organization.- This group is responsible for enterprise-wide innovation and is not a digital innovation team. New technology might be an outcome of these initiatives, but they are really looking for someone who can look at a program with a wider scope than just tech, and can communicate with senior leaders. This is not an IT project manager position.- This person will be leading very large pilots and transformation programs. They are responsible for taking pilots to market and demonstrating market value. They should be able to speak to specific experience with this. Large program management experience is a must, but they also need to have a more granular PM skillset to actually drive the project.- It is essential that they have excellent communication, including experience working with senior leadership and managing complex personalities and relationships across an organization.- This group has a future-thinking/ start-up culture. From a soft-skill perspective, this person should also be comfortable working in ambiguous grey areas and “wearing many hats.” Looking for a personality fit with a “can-do” attitude.- Basic Requirements are 5+ years healthcare and 5+ years program management (Those are the two dropdown skillsets for the submittals). They should have experience using Excel, MS project, Powerpoint, and some PM software. A MPH or MBA would be a pPowered by JazzHRaMDC5zRL0z

Full Time
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Viral Vector - Upstream Pilot
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Full Time
location-iconWinthrop MA
Job Description

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 Description

At Takeda, we are a forward-looking, world-class R&D organization that unlocks innovation and delivers transformative therapies to patients. By focusing R&D efforts on four therapeutic areas and other targeted investments, we push the boundaries of what is possible in order to bring life-changing therapies to patients worldwide.

Join Takeda as a Viral Vector - Upstream Pilot where you will be an important member within a small group responsible for owning and performing non-GMP Pilot upstream cell culture operations within a viral vector lab supporting both cell and gene therapy groups. You will also lead vial thaw, expansion, and production of both adherent cultures in cultures in flask/stack operation and suspension cultures, harvest, and filtration of batches to support development and clinical timelines. As part of the Viral Vector Pilot Operations and Scaleup Sciences, you will report to Associate Director CMC and work with upstream and downstream pilot team and with the process development and in-process analytics teams.

How you will contribute:

  • Cell culture (seed train/expansion/production bioreactor), harvest operations (filtrations or centrifugation), media/buffer planning and ordering, scheduling, large-scale column packing, sample forecasting and submission, metabolite or sample measurement, assisting with assembly and disassembly of process equipment, authoring batch records/SOPs or proposing document revisions, and execution of these records in both a cGMP and a non-GMP environment.

  • Contribute to all technical operations within the Viral Vector Lab (VVL) for the upstream unit operations, both adherent and suspension, and process monitoring and data acquisition.

  • Help create material supply campaign plans and coordination efforts with Cell and Gene therapy teams to meet timeline and quantity demands.

  • Participate in most aspects of tech transfer from non-GMP Pilot team of cell culture process for biologics production into cGMP manufacturing stage.

  • Document data in laboratory notebooks and batch records completely following established company guidelines/SOPs. Write documents such as reports, protocols and internal presentations that may require substantial edits.

  • Help lead studies and technology evaluations that lead to IP, publications, external abstracts and presentations at industry events and conferences.

  • Organize and present issues and results at departmental and project meetings.

  • Interpret data and contribute to technical reports.

  • Contribute to the design of new applications/experiments/unit operations in consultation with manager.

  • Support technology transfer through writing and consolidating technical documents.

  • Contribute to the non-GMP upstream efforts and responsible for independently preparing and executing routine and complex experiments and unit operations.

  • Plan unit operations and experiments drafting support documentation (SOPs, batch records, and/or reports).

  • Collaborate within the framework of cross-functional process development teams including engineers and manufacturing teams.

  • Lift, pull or push equipment requiring up to 25-75 lbs of force.

Minimum Requirements/Qualifications:

  • Associate degree in chemical engineering, biotechnology, chemistry, biology, pharmacy, engineering, or related pharmaceutical science and 4+ years relevant industry experience.

  • Bachelor's degree in chemical engineering, biotechnology, chemistry, biology, pharmacy, engineering, or related pharmaceutical science; 2+ years relevant industry experience.

  • Master's degree in chemical engineering, biotechnology, chemistry, biology, pharmacy, engineering, or related pharmaceutical science; 0+ years relevant industry experience.

  • Previous experience working in manufacturing or lab setting or master's degree plus appropriate laboratory training.

  • Experience with cell culture is required with purification experience also desired, as this role will support both upstream and downstream operations.

  • Experience with cell culture and aseptic techniques.

  • Experience with laboratory equipment that supports cell culture, such as bioreactors and/or adherent culture stacks, metabolite analyzers, shake flasks, cell culture plates.

  • Experience using automation preferred.

  • Experience with electronic batch record system preferred.

  • Experience with chromatographic and other protein separation principles.

  • Familiarity with use of bio-separation equipment and standard analytical assays.

  • You must be customer-focused, results oriented, science-driven, and have high attention to detail.

What Takeda can offer you:

  • Comprehensive Healthcare: Medical, Dental, and Vision

  • Financial Planning & Stability: 401(k) with company match and Annual Retirement Contribution Plan

  • Health & Wellness programs including onsite flu shots and health screenings

  • Generous time off for vacation and the option to purchase additional vacation days

  • Community Outreach Programs and company match of charitable contributions

  • Family Planning Support

  • Flexible Work Paths

  • Tuition reimbursement

More 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.

#LI-SB1

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.

Locations

Boston, MA

Worker Type

Employee

Worker Sub-Type

Regular

Time Type

Full time
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Viral Vector - Upstream Pilot
share-icon
Full Time
location-iconWinthrop MA
Job Description

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 Description

At Takeda, we are a forward-looking, world-class R&D organization that unlocks innovation and delivers transformative therapies to patients. By focusing R&D efforts on four therapeutic areas and other targeted investments, we push the boundaries of what is possible in order to bring life-changing therapies to patients worldwide.

Join Takeda as a Viral Vector - Upstream Pilot where you will be an important member within a small group responsible for owning and performing non-GMP Pilot upstream cell culture operations within a viral vector lab supporting both cell and gene therapy groups. You will also lead vial thaw, expansion, and production of both adherent cultures in cultures in flask/stack operation and suspension cultures, harvest, and filtration of batches to support development and clinical timelines. As part of the Viral Vector Pilot Operations and Scaleup Sciences, you will report to Associate Director CMC and work with upstream and downstream pilot team and with the process development and in-process analytics teams.

How you will contribute:

  • Cell culture (seed train/expansion/production bioreactor), harvest operations (filtrations or centrifugation), media/buffer planning and ordering, scheduling, large-scale column packing, sample forecasting and submission, metabolite or sample measurement, assisting with assembly and disassembly of process equipment, authoring batch records/SOPs or proposing document revisions, and execution of these records in both a cGMP and a non-GMP environment.

  • Contribute to all technical operations within the Viral Vector Lab (VVL) for the upstream unit operations, both adherent and suspension, and process monitoring and data acquisition.

  • Help create material supply campaign plans and coordination efforts with Cell and Gene therapy teams to meet timeline and quantity demands.

  • Participate in most aspects of tech transfer from non-GMP Pilot team of cell culture process for biologics production into cGMP manufacturing stage.

  • Document data in laboratory notebooks and batch records completely following established company guidelines/SOPs. Write documents such as reports, protocols and internal presentations that may require substantial edits.

  • Help lead studies and technology evaluations that lead to IP, publications, external abstracts and presentations at industry events and conferences.

  • Organize and present issues and results at departmental and project meetings.

  • Interpret data and contribute to technical reports.

  • Contribute to the design of new applications/experiments/unit operations in consultation with manager.

  • Support technology transfer through writing and consolidating technical documents.

  • Contribute to the non-GMP upstream efforts and responsible for independently preparing and executing routine and complex experiments and unit operations.

  • Plan unit operations and experiments drafting support documentation (SOPs, batch records, and/or reports).

  • Collaborate within the framework of cross-functional process development teams including engineers and manufacturing teams.

  • Lift, pull or push equipment requiring up to 25-75 lbs of force.

Minimum Requirements/Qualifications:

  • Associate degree in chemical engineering, biotechnology, chemistry, biology, pharmacy, engineering, or related pharmaceutical science and 4+ years relevant industry experience.

  • Bachelor's degree in chemical engineering, biotechnology, chemistry, biology, pharmacy, engineering, or related pharmaceutical science; 2+ years relevant industry experience.

  • Master's degree in chemical engineering, biotechnology, chemistry, biology, pharmacy, engineering, or related pharmaceutical science; 0+ years relevant industry experience.

  • Previous experience working in manufacturing or lab setting or master's degree plus appropriate laboratory training.

  • Experience with cell culture is required with purification experience also desired, as this role will support both upstream and downstream operations.

  • Experience with cell culture and aseptic techniques.

  • Experience with laboratory equipment that supports cell culture, such as bioreactors and/or adherent culture stacks, metabolite analyzers, shake flasks, cell culture plates.

  • Experience using automation preferred.

  • Experience with electronic batch record system preferred.

  • Experience with chromatographic and other protein separation principles.

  • Familiarity with use of bio-separation equipment and standard analytical assays.

  • You must be customer-focused, results oriented, science-driven, and have high attention to detail.

What Takeda can offer you:

  • Comprehensive Healthcare: Medical, Dental, and Vision

  • Financial Planning & Stability: 401(k) with company match and Annual Retirement Contribution Plan

  • Health & Wellness programs including onsite flu shots and health screenings

  • Generous time off for vacation and the option to purchase additional vacation days

  • Community Outreach Programs and company match of charitable contributions

  • Family Planning Support

  • Flexible Work Paths

  • Tuition reimbursement

More 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.

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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.

Locations

Boston, MA

Worker Type

Employee

Worker Sub-Type

Regular

Time Type

Full time