QA Investigations Lead II: Cell Therapy Compliance
Legendcareers
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 Bachelor’s degree and has 2-4 years of relevant experience, preferably in quality assurance or clinical quality within aseptic manufacturing. Benefits include medical coverage, a 401(k) plan, and paid parental leave. #J-18808-Ljbffr Legendcareers
Vacancy posted 1 day ago
Similar jobs that could be interesting for youBased on the QA Investigations Lead II: Cell Therapy Compliance in Raritan, NJ vacancy
$68.05k - $109.87k
Legend Biotech in Raritan, NJ is seeking a QA Investigations Lead I to oversee quality investigations for a sterile GMP environment. This role... ...candidate will work independently while ensuring compliance with manufacturing standards. Responsibilities include managing...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
$68.05k - $109.87k
...Jersey, we are developing advanced cell therapies across a diverse array of technology... ...myeloma. Legend Biotech is seeking QA Investigations Lead I as part of the Quality team based... ...inspections and audits as needed. Support compliance activities for site quality...SuggestedPermanent 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...Suggested- 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...Suggested
$83.71k - $109.87k
Legend Biotech US, based in Raritan, NJ, is seeking a QA Lab Compliance Specialist III to provide oversight of Quality Control Laboratories... ...with various QC teams and managing compliance-related investigations efficiently. The position offers a comprehensive benefits package...- Legend Biotech in Raritan, New Jersey is seeking a QA Lab Compliance specialist III to oversee quality and compliance for Quality Control Laboratories. The role requires strong knowledge of cGMP regulations, experience in QA, and the ability to support regulatory inspections...Work experience placement
- Legend Biotech USA is seeking a QA Laboratory Compliance Specialist III based in Raritan, NJ. This role involves providing quality and compliance oversight for testing Advanced therapy products in collaboration with various Quality Control departments. The ideal candidate...
$224.9k - $272.53k
...production line to the latest breakthroughs in cell therapy, this is work that transforms the... ...Reporting to the Executive Director, Compliance Enabling QMS, this role develops and... ...System elements (audits, inspections, investigations, CAPAs, change management, document...Hourly payFull timeTemporary workPart timeFor contractorsSummer workLive inWork at officeLocal areaRemote workFlexible hoursShift work- ...motivated Director, Quality Compliance, who will contribute... ...individual will be responsible for leading Quality Compliance... ...transfer of late stage/commercial cell therapy products and equipment coming... ...events, CAPAs, and other investigations as they relate to compliance...Flexible hours
$90k - $210k
...manufacturing of cellular therapy products. This individual will lead a group of QC analysts... ...and final product from cell therapy products. They will... ...of Analysis Conduct investigation regarding out of... ...accuracy and regulatory compliance Create/Review and approve...Contract workFor contractorsFlexible hoursCellares
Bridgewater, NJ4 days ago$168.37k - $220.99k
...Headquartered in Somerset, New Jersey, we are developing advanced cell therapies across a diverse array of technology platforms, including... ...Biotech is seeking an Associate Director, Site Quality Compliance Lead as part of the Quality team based in Raritan, NJ....Permanent employmentFull timeTemporary workFor contractorsWork at officeLocal areaWorldwideFlexible hoursShift work- Initial Therapeutics, Inc. is hiring for a QA management role focusing on ensuring compliance within contract manufacturing operations. The role involves oversight of Quality Management Systems, partnering with quality leaders, and supporting validation efforts for drug...Contract work
- ...processes at internal sites and Contract Development and Manufacturing Organizations (CDMO). This role includes leading a Quality Assurance team and ensuring compliance with international regulations. The ideal candidate will have over 10 years of experience in Quality...Contract work
$226.28k - $377.13k
...Organizations (CDMO). The role leads the site’s independent... ...leaders to assure supply and compliance while promoting a culture of... ...for independently overseeing QA functions, including final batch... ...identification, preventive action, and investigation. Ability to conduct...Contract work- ...quality on the plant floor—partnering closely with operations, leading a team of inspectors and technicians, and ensuring every... ...analysis and corrective actions to eliminate defects Lead Audits & Compliance Own internal, customer, and third‑party audits Ensure compliance...
Pretium Packaging
Hillsborough, NJ3 days ago $184.24k - $276.36k
Initial Therapeutics, Inc. is seeking a Director, PV QA DSI to lead the Quality Assurance strategy within Clinical Safety and Pharmacovigilance... ...(CSPV). This role will oversee PV QA activities, ensuring compliance with regulatory requirements while leading a high-performing...- Daiichi Sankyo, Inc. seeks a Director, PV QA DSI to lead the planning and implementation of the Quality Assurance strategy within CSPV in... ...oversight of products with REMS, collaborating with Global Audits, Compliance, Development and Medical QA. The incumbent will drive a...
- ...Control, you'll independently lead and oversee all QC activities... ...projects, deviations, and investigations while ensuring all testing activities... ..., Regulatory Affairs, QA, and Supply Chain to support... ...completeness, accuracy, and compliance with internal and external standards...Full timeContract workWork at officeFlexible hours
Insmed
Bridgewater, NJ4 days ago - ...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
LanceSoft
Raritan, NJ12 hours ago - ...• Strong experience in managing automation test projects • Team lead experience with offshore - onshore model • Client facing with strong... ...strategies, plans, and maintain automation test data • Implement QA process and Automated testing for all the work streams to improve...
3B Staffing LLC
Raritan, NJ3 days ago $90k - $120k
Biocodex is seeking a Manager of Quality & Pharmaceutical Affairs in Bedminster, NJ, to support quality and regulatory compliance for dietary supplements and drug products. The ideal candidate has over 10 years in quality compliance and must coordinate with cross-functional...Permanent employmentFull time- MDAEdge is seeking a Business Analyst to assist with Business Sim/UAT testing in Raritan, New Jersey. The successful candidate will be responsible for data preparation and execution of testing scenarios from ICS to TransAct S4 Signify and ensure coordination with IT and...
$137k - $140k
...responsible for managing quality control laboratory activities to ensure timely deliveries for production. Key tasks include overseeing compliance with GMP standards, managing laboratory procedures, and providing feedback to staff. The ideal candidate should hold a Bachelor's...$17.33 - $20.8 per hour
Quality Assurance Coordinator Req #: 0000246456 Category: Quality / Patient Safety Status: Full-Time Shift: Day Facility: RWJ New Brunswick Department: Dietary-Management Pay Range: $17.33 - $20.80 per hour Location: One Robert...Hourly payFull timeTemporary workFlexible hoursShift workWeekend workRWJBarnabas Health
New Brunswick, NJ2 days ago- ...dealing with global market registrations and providing regulatory compliance/Affairs guidance, and support to all External Manufacturing... ...organizations, and global personnel such as CMC. * Participating in other QA supporting activities as required (e.g. internal audits, site...Contract workLocal areaWorldwide
Omni Inclusive
New Brunswick, NJ4 days ago - ...This position is responsible for leading Go!Foton's Quality Assurance function located at its headquarters, ensuring the quality of... ...crucial role in identifying and resolving quality issues, ensuring compliance with industry standards and regulations, and contributing to...Contract workOverseasFlexible hours
Go!Foton
Somerset, NJ2 days ago - Colgate is seeking a Director, Quality for Skin Health based in Piscataway, New Jersey. This hybrid position requires leading regulatory compliance and quality initiatives across the division while collaborating with various teams to ensure product excellence. The successful...
$156k - $200k
...-Palmolive is seeking a Director, Quality for Skin Health in Piscataway, New Jersey. This role is crucial for overseeing quality compliance and improvement initiatives across the Skin Health division. The ideal candidate will have a Bachelor's degree and 12+ years of experience...- Sun Pharma is seeking a qualified leader to oversee QA and QC operations in New Brunswick, New Jersey. The position requires ensuring compliance with cGMP standards and managing quality goals aligned with global objectives. Applicants should have a Bachelor's degree in...
Do you want to receive more vacancies?
Subscribe and receive similar vacancies to QA Investigations Lead II: Cell Therapy Compliance. Be the first to apply!
Related searches
- quality assurance representative Raritan, NJ
- lead qa Raritan, NJ
- quality assurance team leader Raritan, NJ
- director quality assurance Raritan, NJ
- quality assurance Raritan, NJ
- quality assurance auditor Raritan, NJ
- qa Raritan, NJ
- director quality assurance regulatory affairs Raritan, NJ
- pharmaceutical quality assurance Raritan, NJ
- qa architect Raritan, NJ