QA Investigations Lead II - Cell Therapy Quality & CAPA
$68.05k - $109.87kMerck
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.
- 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
- Legend Biotech seeks a QA Investigations Lead I to oversee quality investigations in Raritan, NJ. This role involves ensuring robust investigations in a GMP environment, supporting regulatory compliance, and collaborating with various teams. The ideal candidate holds a...Quality
$68.05k - $109.87k
...Jersey, we are developing advanced cell therapies across a diverse array of... ...myeloma. Legend Biotech is seeking QA Investigations Lead I as part of the Quality team based in Raritan, NJ . Role... ...Corrective and Preventative Actions (CAPA’s) are developed and implemented....QualityPermanent employmentFull timeTemporary workFor contractorsWork experience placementLocal areaWorldwideFlexible hours$61.45k - $80.66k
A leading biotechnology company in Raritan, NJ seeks a QA Investigations Lead I. Responsibilities include overseeing quality investigations and ensuring compliance within a GMP environment. Ideal candidates should possess a Bachelor’s Degree and 2-4 years of relevant experience...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
- Legend Biotech, located in Raritan, NJ, is seeking a QA Laboratory Compliance Specialist III to oversee quality control laboratories and ensure all practices comply with global regulatory requirements. The ideal candidate will have at least 2 years of relevant experience...Quality
- 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 US is seeking a QA Shop Floor Specialist in Raritan, New Jersey, to provide quality oversight in the production of CAR-T products. This exempt-level... ...issues, manage documentation, and support investigations. A Bachelor’s degree in Life Sciences or Engineering...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$83.71k - $109.87k
...Biotech US, based in Raritan, NJ, is seeking a QA Lab Compliance Specialist III to provide oversight of Quality Control Laboratories. This role involves ensuring... ...QC teams and managing compliance-related investigations efficiently. The position offers a comprehensive...Quality- 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
- Legend Biotech is hiring a QA Shop Floor Specialist in Raritan, New Jersey. This role is responsible for quality oversight of CAR-T product production. The Specialist will ensure compliance with cGMP standards, support audits, and work with cross-functional teams to maintain...Quality
- Legend Biotech is seeking a QA Shop Floor Specialist in Raritan, New Jersey. This role entails overseeing quality in the production of CAR-T products within a cGMP cleanroom. Candidates must have a Bachelor's degree and experience in aseptic manufacturing. Responsibilities...QualityDay shift
$90k - $210k
...as the Manager of Quality Control at our GMP... ...manufacturing of cellular therapy products. This individual will lead a group of QC... ...final product from cell therapy products. They... ...Conduct investigation regarding out of specifications... ..., Deviation, CAPA, Audits, Quality Metrics...QualityContract workFor contractorsFlexible hours- 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
- Legend Biotech is seeking a QA Shop Floor Specialist based in Raritan, New Jersey. This exempt level position focuses on quality oversight in the production of CAR-T products within a controlled cGMP cleanroom environment. Ideal candidates should have a Bachelor’s degree...Quality
$96.27k - $126.35k
...Jersey, we are developing advanced cell therapies across a diverse array of... ...treatment of multiple myeloma. QA Shop Floor Specialist as part of the Quality Operations team based in Raritan... ...proactively driving compliance. Support investigations team by providing quality and...QualityWork experience placementLocal areaImmediate startWorldwideFlexible hoursWeekend workDay shift$96.27k - $126.35k
...Jersey, we are developing advanced cell therapies across a diverse array of... ...Opening Legend Biotech is seeking a QA Shop Floor Specialist as part of the Quality Operations team based in Raritan... ...quality and compliance input for investigations, continuous improvement, and...QualityTemporary workImmediate startWorldwideFlexible hoursWeekend workAfternoon shift$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$83.71k - $109.87k
...develop advanced cell therapies across a diverse array... ...myeloma. QA Laboratory Compliance... ...position responsible for quality and compliance... ...Services, and QC Investigations. Key Responsibilities... ...and coach Level I/II QALC on day‑to‑day... ...corrections, CAPA actions, and root‑...QualityTemporary workWork experience placementWork at officeWorldwideFlexible hours$83.71k - $109.87k
...developing advanced cell therapies across a diverse... ...multiple myeloma. The QA Lab Compliance... ...III is part of the Quality team based in... ...Lab Services and QC Investigations. Key Responsibilities... ...and coach Level I/II QALC when... ...corrections, and CAPAs. Provide guidance...QualityTemporary workWork experience placementWork at officeLocal areaImmediate startWorldwideFlexible 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- ...creative, and detail-oriented Quality Control Analyst to join our... ...stability samples Work with cell therapy products and associated... ...discrepancies, initiate and investigate OOS/OOT results for phase 1 and... ...; change control, deviation, CAPA, audits, quality metrics, etc...QualityFlexible hours
- ...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
- ...and operationally rigorous Quality Control Raw Material Analyst... ...OOT) results; initiate formal investigations in the QMS and participate... ...deviation investigations and CAPAs associated with raw material... ...integrated technologies for cell therapy manufacturing to accelerate...QualityContract workFlexible hours
- Legend Biotech USA is seeking a QA Laboratory Compliance Specialist III... ...NJ. This role involves providing quality and compliance oversight for testing Advanced therapy products in collaboration with... ...ability to manage nonconformance and CAPA processes. On-site presence is...Quality
$224.9k - $272.53k
## Senior Director, GxP Training Quality & ComplianceNew Brunswick - NJ - USFind out... ...line to the latest breakthroughs in cell therapy, this is work that transforms the... ...System elements (audits, inspections, investigations, CAPAs, change management, document management...QualityHourly payFull timeTemporary workPart timeFor contractorsSummer workLive inWork at officeLocal areaRemote workFlexible hoursShift work$70k - $75k
...important medicines. The Quality Assurance Specialist is a... ..., reviewing deviations, CAPAs, chance controls, validation... ...include SOPs, deviation/investigation reports, equipment/system... ...Previous experience for QA I (0 to 2 years or more), QA II (2 to 5 years or more),...QualityFull timeWork at officeLocal areaFlexible hours
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