Senior Sterility Assurance Manager - Cell Therapy
$121.07k - $146.7kVetJobs and Military Spouse Jobs
VetJobs and Military Spouse Jobs is seeking a Sr. Manager, Sterility Assurance in Summit, NJ. You will manage critical processes supporting CAR T manufacturing and ensure compliance with regulatory standards. Ideal candidates should possess advanced knowledge of cGMP's and FDA regulations, strong managerial skills, and have experience with cell therapy products. Compensation for this role ranges from $121,070 - $146,703. #J-18808-Ljbffr VetJobs and Military Spouse Jobs
- ...Bristol-Myers Squibb is looking for a Senior Manager, Sterility Assurance in Summit, NJ. This pivotal role will manage the Sterility Assurance for... ...strong leadership skills, and have previous experience in cell therapy. This position offers various benefits such as health...SeniorFlexible hours
- Bristol Myers Squibb in Summit, NJ is seeking a Senior Specialist, QC Microbiology, Cell Therapy to support in-process, final product, and stability testing and environmental monitoring. You will perform method transfers, troubleshooting, data review, CAPA and deviations...Senior
- Director, Regulatory CMC - Cell Therapy Overview Responsible for overseeing management of multiple development and life-cycle management projects of varying priorities... ...regulatory strategy, issues, and risks to senior leadership and governing bodies Experience as a CMC...SuggestedShift work
$199.95k - $242.3k
## Director, Regulatory CMC - Cell TherapyMadison - Giralda - NJ... ...latest breakthroughs in cell therapy, this is work that transforms... ...responsible for overseeing management of multiple development and life... ...verbal format to regulatory senior leadership team and other...SuggestedHourly payFull timeTemporary workPart timeFor contractorsSummer workLive inWork at officeLocal areaRemote workFlexible hoursShift work$199.95k - $242.3k
...optimizing production lines to advancing cell‑therapy breakthroughs. Job Summary The GRS‑CMC... ...multiple development and lifecycle management projects, represents the organization on... ...regulatory strategy, issues, and risks to senior leadership and governing bodies...SuggestedFull timeShift work$121.07k - $146.7k
## Senior Manager, Sterility AssuranceSummit West - NJ - USFind out how well you match with this job... ...line to the latest breakthroughs in cell therapy, this is work that transforms the... ...Summary**The Sr. Manager, Sterility Assurance, is a highly critical role and is responsible...SeniorHourly payFull timeTemporary workPart timeFor contractorsSummer workLive inWork at officeLocal areaRemote workFlexible hoursShift work- Bristol-Myers Squibb is seeking a Director, Regulatory CMC for Cell Therapy in Madison, NJ. In this pivotal role, you will oversee multiple development and lifecycle management projects, ensuring regulatory compliance and strategic direction in alignment with global guidelines...
- Bristol Myers Squibb EU Policy is seeking a Director for Regulatory CMC in Cell Therapy. In this role, you will oversee management of multiple development projects, represent GRS-CMC in cross-functional teams, and ensure compliance with regulatory requirements. The ideal...
- Bristol-Myers Squibb is seeking a Senior Specialist in QC Microbiology based in Summit, NJ. This role focuses on supporting QC testing, environmental monitoring, and method validation. Ideal candidates will have substantial microbiological testing experience and a strong...Senior
$40.97 - $49.64 per hour
Senior Specialist, QC Microbiology, Cell Therapy Position Summary: Responsible for supporting QC testing for in-process, final product, stability samples... ...Ability to communicate effectively with peers, department management and cross‑functional peers about task status,...SeniorHourly payFull timeTemporary workSummer workFlexible hours- ...and ensuring compliance with cGMP standards. Candidates should possess at least 15 years of experience in Quality and Compliance management, with excellent communication skills and the ability to lead teams. Competitive compensation and numerous benefits, including flexible...SeniorContract workFlexible hours
$199.95k - $242.3k
...represent the organization on cross-functional teams. This role is essential in ensuring compliance with global regulatory guidelines and managing the growth of direct reports. The ideal candidate will have a BA/BS degree, 10 years of relevant experience, and expertise in CMC...$40.97 - $49.64 per hour
## Senior Specialist, QC Microbiology, Cell TherapySummit West - NJ - USFind out how well you match with this job... ...the latest breakthroughs in cell therapy, this is work that transforms the lives... ...effectively with peers, department management and cross-functional peers about...SeniorHourly payFull timeTemporary workPart timeFor contractorsSummer workLive inWork at officeLocal areaRemote workFlexible hoursShift work$238.2k - $288.64k
...Manufacturing Quality, Cell Therapy Position Summary... ...Contract Test Labs (CTLs) management for the Cell Therapy... ...a team of Quality Senior Directors or others in... ...Ensures the Quality Assurance Agreements for Suppliers... ...manufacturing, sterility assurance, chemical and...SeniorHourly payFull timeContract workTemporary workPart timeFor contractorsSummer workWork at officeLocal areaRemote workFlexible hoursShift work- Bluecrux is seeking a SaaS Implementation Manager to lead strategic implementations of Binocs, our cutting-edge SaaS solution for laboratories and cell & gene therapy teams. You will manage end-to-end implementation projects, guide customers through onboarding, and engage...SeniorLive in
$120k - $150k
Shionogi Inc. is seeking a QA Product Manager for Sterile Products in Florham Park, NJ. This critical role ensures the quality, safety, and... ...Life Sciences, at least five years in pharmaceutical Quality Assurance, and experience with sterile products. Competitive salary range...$120k - $145k
...partnerships with manufactures from around the world. About the Role This position reports to the Vice President, Quality Assurance and will manage or support: cGMP compliance assessment of contract manufacturers, the company SOP and Training systems, QA/QC Testing /...SeniorContract workFlexible hours$240.94k - $291.96k
...production line to the latest breakthroughs in cell therapy, this is work that transforms the lives... ...area, with a primary focus on management of pulmonology asset and associated Health... ...and external regulatory resources to assure regulatory issues are addressed in development...Full timeTemporary workRemote work$120k - $150k
...(U.S.) in Florham Park, NJ, is seeking a QA Product Manager to ensure quality and compliance of sterile pharmaceutical products. The ideal candidate will have at least five years of pharmaceutical Quality Assurance experience, lead technology transfer projects, and manage...$45 - $59 per hour
Job Title QA Product Manager (Sterile Products) Location Florham Park, New Jersey Type Contract Compensation $45-$59 per hour dependent... ...in batch record review, CAPA management, and sterility assurance. Direct experience with third‑party (CMO) oversight. Able...Hourly payOngoing contractContract workFor contractorsZero hours contractLocal areaRemote work- System One is seeking a QA Product Manager to oversee quality assurance for sterile products. Based in Florham Park, New Jersey, this role involves reviewing batch records, managing CAPAs, and coordinating investigations. Candidates should have a minimum of 4 years of...
$120k - $150k
Overview The QA Product Manager (Sterile Products) plays a critical role in ensuring the quality, safety, and regulatory compliance of sterile... ...build andmaintainrobust quality systems, support sterility assurance and contamination control strategies, and uphold regulatory...Full timeWork at officeLocal area$121.07k - $146.7k
...location detailed in the job post. Position Summary The Sr. Manager, Sterility Assurance, is a highly critical role and is responsible for... ...regulations and guidelines, as related to manufacture of cell therapy products. Advanced data integrity knowledge and practices...SeniorFlexible hoursShift work- Merck in Rahway, NJ seeks a Senior Scientist to join the Process Cell Sciences group. You will help develop and characterize mammalian production cell lines to support the biologics pipeline and manufacturing processes for clinical trials and commercialization. The role...Senior
$126k - $176k
A growing food production company in Linden, NJ is seeking a Senior Quality Assurance Manager to ensure compliance with quality and safety regulations. The ideal candidate will have over 10 years of experience in the food industry, strong leadership skills, and a Bachelor...Senior$135.77k - $164.52k
...lives. Our purpose is to discover and develop therapies that will change the course of human health. The Senior Manager, CTTO Analytical Lab will manage an analytical... ...Experience with various bioanalytical techniques (cell‑based assays, ELISA, qPCR, flow cytometry) and...SeniorHourly payFull timeTemporary workWork experience placementSummer workRemote workFlexible hoursShift work- Admera Health is looking for a Senior Scientist in South Plainfield, NJ, to join its Single-Cell & Spatial Genomics platform team. The ideal candidate will have a PhD in a related field or a Master's with relevant experience, with hands-on skills in NGS, single-cell RNA...Senior
- Merck & Co. is seeking a Senior Technician for operations at their Rahway, NJ location. This first shift position involves supporting drug product development through sterile filling, lyophilization, and GMP compliance. The technician will work closely with formulators...SeniorDay shift
- I am leading a search for a Senior Director, Global Regulatory Clinical Strategy at a commercial... ...organization focused on non-opioid pain management and regenerative health solutions, with... ...small molecules, biologics, and gene therapy. This is a highly visible leadership...Senior
- Merck in Rahway, NJ is looking for a Senior Technician for Operations. The role involves supporting drug product development through hands-on activities such as sterile filling and equipment operation in a GMP-regulated environment. The ideal candidate has at least 2 years...SeniorDay shift
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