Cell Therapy QA Investigations Lead
Dormont Manufacturing Company
Legend Biotech in Raritan, NJ is seeking a QA Investigations Lead I to provide quality oversight for personalized cell therapy production in a GMP environment. The ideal candidate will demonstrate excellence in quality, collaborate with various teams, and handle investigations effectively. Responsibilities include managing investigations, ensuring compliance with quality standards, and supporting regulatory inspections. The role requires a Bachelor’s degree and 2-4 years of relevant experience. A comprehensive benefits package is offered, highlighting health insurance and retirement plans. #J-18808-Ljbffr Dormont Manufacturing Company
- 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
$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$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 demands attention to detail and the ability to collaborate in a team setting. The successful candidate will work independently...Suggested- 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...Suggested
$61.45k - $80.66k
...Headquartered in Somerset, New Jersey, we are developing advanced cell therapies across a diverse array of technology platforms, including... ...and cutting‑edge therapeutics for patients worldwide. QA Investigations Lead I Location: Raritan, NJ Role Overview The QA...SuggestedFull timeTemporary workWork experience placementWorldwideFlexible hours- 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...
$90k - $210k
...the GMP manufacturing of cellular therapy products. This individual will lead a group of QC analysts performing... ...in-process and final product from cell therapy products. They will interface... ...of Analysis Conduct investigation regarding out of specifications (OOS...Contract workFor contractorsFlexible hours$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...$226.28k - $377.13k
...we are advancing breakthrough therapies in oncology, cardiovascular... ...Organizations (CDMO). The role leads the site's independent... ...responsible for the independent QA function, with authority for... ...complaint management, root‑cause investigations, and reporting of critical GMP...Contract workLocal area- 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...
- ...will focus on quality management systems, process validation, and complaint investigation. Ideal candidates have extensive pharmaceutical experience and knowledge in drug manufacturing and QA compliance. This position is poised for impact in a collaborative environment...Contract work
- 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
$224.9k - $272.53k
...optimizing a production line to the latest breakthroughs in cell therapy, this is work that transforms the lives of patients, and the... ...with Quality Management System elements (audits, inspections, investigations, CAPAs, change management, document management).* Strong...Hourly payFull timeTemporary workPart timeFor contractorsSummer workLive inWork at officeLocal areaRemote workFlexible hoursShift work- ...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...Flexible hours
- 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
- ...oversee the quality 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...Contract work
$201.43k - $244.09k
...the latest breakthroughs in cell therapy, this is work that transforms... ...product development programs Lead remediation plans following... ...complex cross-site microbiological investigations, CAPA development, and... ...manufacturing environments (production, QA, and/or validation), with...Hourly payFull timeTemporary workPart timeFor contractorsSummer workLive inWork at officeLocal areaRemote workFlexible hoursShift 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
$124k
...Director, Quality Control, you'll independently lead and oversee all QC activities conducted... ...analytical projects, deviations, and investigations while ensuring all testing activities are... ...Development, Regulatory Affairs, QA, and Supply Chain to support product development...Full timeContract workWork experience placementWork at officeLocal areaFlexible hours- ...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
$155k
...appropriate GMP compliance principles to quality decisions. Lead investigations, CAPAs, deviations and quality events to resolution and... ...responsible for release or rejection of GMP materials and utilize QA staff to manage the timeline and assure on time delivery of...Contract workWork experience placementLocal areaRemote workFlexible hours$137k - $140k
Merck & Co. is seeking a Manager for its QC Lab in Piscataway, NJ. This role is responsible for managing quality control laboratory activities to ensure timely deliveries for production. Key tasks include overseeing compliance with GMP standards, managing laboratory procedures...$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 work$130k - $160k
...industry and corporate standards. Build, mentor, and lead a high-performing quality assurance and quality control (QA/QC) team, fostering a culture of collaboration and accountability. Empower team to lead investigations into deviations, CAPA (Corrective and Preventive...Hourly payWork experience placementFlexible hours- ...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
- ...seeks a Head of Quality Assurance to oversee the quality oversight of internal sites and CDMO. This role is responsible for managing QA functions, ensuring compliance with global standards, and driving continuous improvements. The ideal candidate will have over 10 years...
$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...$90k - $120k
...compliance throughout the organization and leading continuous improvement efforts.* Serving... ...organizations and representing QA during manufacturing campaigns.* Reviewing... ...Collaborating with stakeholders on deviation investigations, CAPA plans, root cause analysis...Permanent employmentFull timeContract workTemporary workLocal areaFlexible hours2 days per week- The Senior Embedded Device Test Lead plays a critical role in the testing and validation process of embedded systems, ensuring high-quality... ...in embedded device functionalities. Develop, guide, and mentor QA engineers in utilizing the embedded device testing framework,...
- HCL Technologies Limited is seeking a Senior Embedded Device Test Lead to ensure high-quality deliverables in embedded systems testing.... ...responsibilities include overseeing automated test script execution, mentoring QA engineers, and identifying testing process improvements....
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