QA Investigations Lead - Cell Therapy (II/III)
$70.67k - $99.71kLegend Biotech
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. A Bachelor’s degree and 2-4 years of experience in quality assurance are required. The position offers a base pay range of $70,671 to $99,713, along with additional benefits including performance bonuses and comprehensive insurance plans. #J-18808-Ljbffr Legend Biotech
- 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...Suggested
$70.67k - $99.71k
...Biotech is a global biotechnology company dedicated to treating life‑threatening diseases with advanced cell therapies. Role Overview The QA Investigation Lead (II/III) is an exempt level position reporting to the QA Investigation Supervisor within the Raritan...SuggestedTemporary workWork experience placementLocal areaFlexible hours$70.67k - $99.71k
...Headquartered in Somerset, New Jersey, we are developing advanced cell therapies across a diverse array of technology platforms,... ...of multiple myeloma. Legend Biotech is seeking a QA, Investigations Lead II/III as part of the Quality team based in Raritan, NJ. Role...SuggestedPermanent employmentFull timeTemporary workFor contractorsWork experience placementLocal areaWorldwideFlexible 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...Suggested- Legend Biotech is hiring a QA Investigations Lead I for their Raritan, NJ location. This exempt position focuses on providing quality oversight... ...of events in the production of personalized cell therapy products. The role requires a Bachelor's Degree in a relevant...SuggestedFull time
- Legend Biotech USA is seeking a Supervisor, QC Investigations in Raritan, NJ. This exempt position entails supervising quality control... ...hiring and developing staff, and managing workflows related to cell therapy manufacturing. The ideal candidate will have a Bachelor’s...
$127.31k - $167.1k
Legend Biotech, 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 highly organized individual with at least 7 years of relevant experience in quality...Full time- 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...
$90k - $210k
...This individual will be responsible for leading Quality Compliance activities for the... ...tech transfer of late stage/commercial cell therapy products and equipment coming through the... ..., quality events, CAPAs, and other investigations as they relate to compliance and technical...Full timeFlexible hours- Must Have - GxP, Regulatory, Regression testing, JIRA-Xray, Functional/ manual testing, Saucelabs for multibrowser testing, data bricks, Spotfire, ISTQB/ CSTE certifications Key Responsibilities: Oversee the testing phase of projects, ensuring that software and...
- Must Have - GxP, Regulatory, Regression testing, JIRA-Xray, Functional/manual testing, Saucelabs for multibrowser testing, Data Bricks, Spotfire, ISTQB/CSTE certifications Key Responsibilities: Oversee the testing phase of projects, ensuring that software and systems meet...
- AgHires is seeking a Food Safety Manager based in Readington Township, New Jersey. The role involves supporting the design and execution of a comprehensive food safety program for distribution and produce manufacturing. Ideal candidates will have extensive experience in...
- ...QA Lead Location: Warren, NJ Duration: Contract Rate: DOE Core skills need candidates with 10+ years of experience: Strong track record of BI/ETL testing with hands-on 10+ years of experience is must. Hands-on 9+ years of experience for writing advanced...Contract work
$116.4k - $174.6k
Initial Therapeutics, Inc. is hiring a Manager for Medical Affairs Quality in Basking Ridge, NJ. This role is critical for operational leadership and quality oversight for Medical Affairs programs, ensuring compliance with high-quality standards within regulatory frameworks...- .... Candidates should have a Bachelor's Degree and at least 3 years of experience in data management roles. Responsibilities include leading project teams, overseeing data quality, and ensuring adherence to regulatory standards. This position offers a dynamic and collaborative...
$190.06k - $230.31k
...From optimizing a production line to the latest breakthroughs in cell therapy, this is work that transforms the lives of patients, and the... ...resource management strategies to optimize operational efficiency. · Lead GQ-wide financial tracking and forecasting, ensuring alignment...Hourly payFull timeTemporary workPart timeFor contractorsSummer workLive inWork at officeLocal areaRemote workFlexible hoursShift work$131.37k - $159.19k
...From optimizing a production line to the latest breakthroughs in cell therapy, this is work that transforms the lives of patients, and the... ...technical as well as business process focused individuals. Ability to lead medium sized projects and enhancements Ability to constantly...Hourly payFull timeTemporary workPart timeFor contractorsSummer workLive inWork at officeLocal areaRemote workWorldwideFlexible hoursShift work- ...Post Market Regulatory Affairs activities associated with complaint handling and MDR submissions. These activities include intake, investigation, documentation, follow-up, regulatory reporting and metrics. The Customer Quality Specialist is responsible for the oversight...Work experience placement
- Bristol Myers Squibb in New Jersey is seeking an experienced Quality Assurance professional with oversight of supplier activities. This role involves managing supplier qualifications and ensuring compliance with GMP standards. Candidates should have at least 5 years of ...Work at officeRemote work
- ...cGMP Operations within a state-of-the-art multi-product cell therapy manufacturing facility that will be utilized to... ...allogeneic cell therapy products. This individual will lead the Quality organization (QA/QC) and partner with other functions to produce cell therapy...Flexible hoursShift work
$102k - $177.1k
Johnson & Johnson is seeking a Manager, Quality & Compliance to lead the quality assurance efforts within its MedTech division in Raritan, New Jersey. This role requires 8+ years of experience in quality management across multi-country operations, focusing on compliance...- ...This position is responsible for leading Go!Foton's Quality Assurance function located at its headquarters, ensuring the quality of both products and services delivered to its customers throughout the entire process. The Go!Foton Quality Assurance Manager (QAM) reports...Contract workOverseasFlexible hours
$17.41 - $18.38 per hour
Job Title Quality Assurance Coordinator Job Reference and Status Req #: 0000245735 • Full‑time • Shift: Day • Facility: RWJ New Brunswick • Department: Dietary‑Management. Location Main Hospital - New Brunswick Pay Hourly: $17.41 - $18.38 per hour. Pay Transparency: ...Hourly payFull timeTemporary workFlexible hoursShift workWeekend work- ...Skilled at interacting with all levels of the organization, excellent communication skills, and inter-personal skills. Skilled at leading cross functionally and motivating direct reports. Experienced problem solver and engage with customers, vendors, and end users....Local area
- ...Our client, a leading organization in the industry, is seeking a EMEA Regional Payroll Workday Test Lead to join their team. As a EMEA Regional Payroll Workday Test Lead, you will be part of the HR Transformation Department supporting global payroll testing initiatives...Weekly payTemporary workRemote workWorldwideFlexible hours
$122k - $212.75k
HR Senior Manager, Quality & Regulatory Affairs DePuy Synthes is recruiting for an HR Sr. Manager, Quality & Regulatory, located in Raynham (MA), Cork (Ireland), Palm Beach Gardens (FL), Warsaw (IN), Leeds (UK), or New Jersey. The HR Senior Manager, Quality & Regulatory...Local areaImmediate start$116.4k - $174.6k
Job Title: Manager, Medical Affairs Quality, RD PV QA Job Summary The Manager, Medical Affairs Quality will provide operational leadership... ...the ethical conduct of interventional, non-interventional, investigator-initiated trials, real world evidence and managed access...Local area- ...support to the VPT's and act as the analytical lead on CMO Technical Transfer Projects.... ...CTL's). Review and approve all laboratory investigations/deviations/Out of Specification (OOS)... ...Previous experience in QC laboratory facing QA activities is highly desirable. Previous...Contract workLocal areaWorldwide
- ...communication pathways with Global Process Owners and Global Process Leads for relevant systems • Act as primary ExM representative at... ...elements, regulatory surveillance Processes include Deviation Investigations, Corrective Action / Preventive Action (CAPA), Complaints,...Permanent employmentContract workFor contractorsWork at officeLocal areaFlexible hours
- RWJBarnabas Health is looking for a Quality Assurance Coordinator in New Brunswick, New Jersey. This full-time role involves checking patient meal trays, preparing tube feedings, and maintaining sanitary conditions. Candidates should have at least a high school diploma ...Full timeWeekend work
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