QA Investigations Lead II - Cell Therapy Quality & CAPA
$68.05k - $109.87kMerck & Co.
Legend Biotech in Raritan, NJ is seeking a QA Investigations Lead I to oversee quality investigations for a sterile GMP environment. This role demands attention to detail and the ability to collaborate in a team setting. The successful candidate will work independently while ensuring compliance with manufacturing standards. Responsibilities include managing investigations, developing CAPAs, and supporting regulatory audits. Benefits include comprehensive health insurance, parental leave, and a performance-based bonus. Salary range is $68,045—$109,870 USD. #J-18808-Ljbffr Merck & Co.
- A leading biotechnology company in Raritan, NJ is seeking a QA Investigations Lead II/III to provide quality oversight during investigations of events in personalized cell therapy production. The role requires a minimum of a Bachelor's degree and 2-4 years of relevant experience...Quality
$68.05k - $109.87k
...QA Investigations Lead II Legend Biotech is a global biotechnology company dedicated... ...we are developing advanced cell therapies across a diverse array of... ...Lead I as part of the Quality team based in Raritan, NJ.... ...and Preventative Actions (CAPA's) are developed and implemented...QualityWork experience placementLocal areaWorldwide$70.67k - $99.71k
A biotechnology company in Raritan is looking for a QA Investigation Lead to provide quality oversight in the production of personalized cell therapy products. The candidate will lead investigations, implement corrective actions, and ensure compliance with cGMP regulations...Quality- Legend Biotech is hiring a QA Investigations Lead I for their Raritan, NJ location. This exempt position focuses on providing quality oversight during investigations of events in the production of personalized cell therapy products. The role requires a Bachelor's Degree...QualityFull time
$70.67k - $99.71k
...threatening diseases with advanced cell therapies. Role Overview The QA Investigation Lead (II/III) is an exempt level position... ...is responsible for providing quality oversight and guidance during investigations... ...and Preventative Actions (CAPA’s) are developed and implemented...QualityTemporary workWork experience placementLocal areaFlexible hours$68.05k - $109.87k
Legend Biotech in Raritan, NJ is looking for a QA Investigations Lead I to provide quality oversight during the investigation of events in the production of cell therapy products. Responsibilities include ensuring timely and accurate investigations, supporting regulatory...Quality- A biotechnology company in Raritan, NJ, is seeking a QA Investigations Lead I to provide quality oversight during investigations in a GMP environment. The... ...ideal candidate will ensure timely investigations, develop CAPAs, and support regulatory audits. Applicants should have...Quality
- ...QA Shop Floor Specialist II Legend Biotech is a global biotechnology company... ...are developing advanced cell therapies across a diverse array of... ...Specialist as part of the Quality Operations team based in... ...driving compliance. Support Investigations team by providing quality...QualityWork experience placementImmediate startWorldwideFlexible hoursWeekend workDay shift
- A global biotechnology company in Raritan, New Jersey, is seeking a QA Shop Floor Specialist II/III to oversee floor quality in the production of CAR-T products. The ideal candidate will have a Bachelor’s degree in Life Sciences and relevant experience in an aseptic manufacturing...Quality
$75.97k - $99.71k
...Jersey, we are developing advanced cell therapies across a diverse array of... ...Overview Legend Biotech is seeking a QA Shop Floor Specialist II/III as part of the Quality Operations team based in... ...driving compliance. Support Investigations team by providing quality and...QualityWork experience placementImmediate startWorldwideFlexible hoursWeekend work- Legend Biotech USA is seeking a Supervisor, QC Investigations in Raritan, NJ. This exempt position entails supervising quality control microbiology laboratories, hiring... ...developing staff, and managing workflows related to cell therapy manufacturing. The ideal candidate will have...Quality
$65k - $104.65k
...Learn more at Job Function Quality Job Sub Function Quality... ...Assurance Incoming Specialist II. This position will be located... ...antigen receptor (CAR) T-cell therapy. This innovative strategic partnership... ...CAR-T platform and investigational treatment. In this role, you...QualityLocal areaImmediate startShift workDay shift- A biotechnology company in New Jersey seeks a QA Change Control Specialist II responsible for quality oversight in a cell therapy manufacturing facility. Applicants should possess a Bachelor's degree in Science and a minimum of two years' experience within a cGMP environment...Quality
$127.31k - $167.1k
...located in Raritan, New Jersey, is seeking a Sr. QA Validation Specialist to oversee validation activities in a cell therapy manufacturing facility. This role requires a... ...at least 7 years of relevant experience in quality assurance or compliance in GMP environments. Key...QualityFull time- Legend Biotech is hiring a QA Shop Floor Specialist in Raritan, New Jersey. This position entails overseeing quality during the production of CAR-T products in a cGMP cleanroom. Responsibilities include ensuring compliance, collaborating with manufacturing teams, supporting...Quality
- Legend Biotech in Raritan, New Jersey, is hiring a QA Shop Floor Specialist. This role involves quality oversight in the production of autologous CAR-T products, ensuring compliance within cGMP standards. The ideal candidate holds a Bachelor’s degree in Life Sciences or...Quality
$70.67k - $92.76k
QA Document Control Specialist I/II/III Legend Biotech is a global biotechnology company dedicated to treating... ..., New Jersey, we develop advanced cell therapies across multiple technology... ...manner consistent with safety policies, quality systems and cGMP requirements. Review...QualityWork experience placementFlexible hours- A biopharmaceutical company is looking for a QA Validation Specialist III in Raritan, NJ. This role involves providing quality oversight for validation activities within a cell therapy manufacturing plant. Candidates should have at least 4 years of experience in quality...Quality
$69.5k - $102.35k
Johnson & Johnson, QA Specialist II (1 of 2) - Application... ...more at Job Function: Quality Job Sub Function:... ...deliver this cutting-edge therapy to our patients. Key... ...are fully investigated and effective corrective... ...systems. Preferred: Cell and Gene Therapy Experience...QualityContract workTemporary workPart timeLocal areaImmediate startAfternoon shift$96.27k - $126.35k
Legend Biotech is seeking a Sr. QC Analyst to join its Quality team in Raritan, NJ. The role involves performing QC testing related to the manufacturing of cell therapy products. Responsibilities include ensuring compliance with GMP regulations and conducting analytical...Quality- Legend Biotech is seeking a Sr. QC Analyst to join their Quality team in Raritan, NJ. This exempt position involves performing quality control testing related to the manufacturing of cell therapy products for clinical trials. The ideal candidate will have a Bachelor’s...Quality
$90k - $210k
...highly motivated Director, Quality Compliance, who will... ...individual will be responsible for leading Quality Compliance... ...of late stage/commercial cell therapy products and equipment coming... ...assessments, quality events, CAPAs, and other investigations as they relate to...QualityFull timeFlexible hours- ...Jersey, we are developing advanced cell therapies across a diverse array of technology... ...a QC Specialist, Lab Services, II/III as part of the Quality team based in Raritan, NJ . Role Overview... ...retained samples. Document and investigate sample‑management nonconformances....QualityPermanent employmentFull timeFor contractorsWork at officeLocal areaWorldwideShift workAfternoon shift
- SUMMARY The Quality Assurance Specialist II is a regular employee in a full-time exempt... ..., reviewing deviations, CAPAs, chance controls,... ...to include SOPs, deviation/investigation reports, equipment/system... ...experience in manufacturing QA support (sampling, room/line...QualityFull timeWork at officeFlexible hours
- Merck & Co. is seeking a QA Shop Floor Specialist in Raritan, NJ for quality oversight during the production of CAR-T products in a cGMP cleanroom environment. Responsibilities include ensuring compliance with company and regulatory standards, reviewing documentation, and...Quality
- Legend Biotech is looking for a Sr. QA Validation Specialist, CSV & Equipment in Raritan... ...for systems and processes in a GMP cell therapy manufacturing plant. Ideal candidates have... ...approving validation documentation, developing quality processes, and providing oversight on...Quality
- Legend Biotech is seeking a Sr. QA Validation Specialist in Raritan, NJ, to provide quality oversight for validation and qualification activities in a cell therapy manufacturing setting. Ideal candidates must possess a Bachelor's Degree in Science and have over 7 years...Quality
- Legend Biotech is seeking a QA Shop Floor Specialist as part of the Quality Operations team based in Raritan, New... ...oversight of all aspects of the cell therapy clinical manufacturing process.... ...conformances proactively. Support investigations by providing quality and...QualityPermanent employmentFull timeFor contractorsLocal areaImmediate startFlexible hoursWeekend workDay shift
$78.25k - $102.71k
Legend Biotech is seeking QC Analyst II as part of the Quality team based in Raritan, NJ . Role Overview The QC Analyst is an exempt level... ...for performing QC testing related to the manufacturing of cell therapy products for clinical trials and commercial operations in...QualityPermanent employmentFull timeTemporary workFor contractorsWork experience placementLocal areaFlexible hoursShift workNight shiftAfternoon shift- A leading biotechnology firm in Raritan, New Jersey, is seeking a QA Document Control Specialist to support the document management process within its manufacturing... ...field and at least 2 years of experience in quality assurance or aseptic manufacturing. This position...Quality
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