QA Compliance Specialist II: GMP & Documentation Expert
Kashiv BioSciences LLC
Kashiv Biosciences LLC in Piscataway Township, New Jersey is seeking a Quality Assurance Specialist. This role involves inspecting, sampling, and testing incoming materials, ensuring compliance with cGMP regulations, and providing quality assurance oversight. The ideal candidate will have a Bachelor’s degree in science or engineering and 0-5 years of relevant quality assurance experience. Strong communication and organizational skills are essential, along with proficiency in Microsoft Office applications. #J-18808-Ljbffr
$70.67k - $92.76k
...QA Document Control Specialist I/II/III Legend Biotech is a global biotechnology company dedicated to treating life‑threatening... ...therapy manufacturing facility. In a sterile GMP environment, the position ensures compliance with the document management system, document...SuggestedWork experience placementFlexible hours- ...BioSciences LLC is looking for a full-time Documentation Specialist to join its Quality Management team in... ...Township, NJ. The role involves managing GMP documents, including SOPs and batch records, as well as ensuring compliance with quality standards. The ideal candidate...SuggestedFull time
- ...The Quality Assurance Specialist II is a regular employee... ...in the facility are in compliance with cGMP requirements... ...and assembling batch documentation, issuing and tracking... ...Ensure adherence to GMP good documentation practices... ...in manufacturing QA support (sampling, room...SuggestedFull timeWork at officeFlexible hours
- Legend Biotech US is seeking a QA Shop Floor Specialist in Raritan, New Jersey, to provide quality... ...level position involves maintaining compliance in a cGMP cleanroom and supporting... ...personnel to resolve quality issues, manage documentation, and support investigations. A...Suggested
$65k - $104.65k
...Quality Assurance Incoming Specialist II. This position will be located... ...to increase quality and compliance and champion increased awareness... ...process Review inspection documentation (C of A or other Material Certifications... ...support in clinical or GMP manufacturing or support of...SuggestedLocal areaImmediate startShift workDay shift- ...development pipeline. We are looking for a Documentation Specialist to join our Piscataway NJ Quality... ...Issuance, Archival and maintain of all GMP documents like SOP, Batch Record, Forms... ...minimum 3 years of related experience. Expert knowledge of scientific principles and...Full timeLocal areaFlexible hours
- ...QA Shop Floor Specialist II Legend Biotech is a global biotechnology company dedicated to treating... ...the highest standards in compliance within company policies, procedures,... ...manufacturing quality issues. Review of all documentation, in accordance with Good...Work experience placementImmediate startWorldwideFlexible hoursWeekend workAfternoon shift
$69.5k - $102.35k
Johnson & Johnson, QA Specialist II (1 of 2) - Application via WayUp Join to apply for the Johnson... .... Perform review of production documentation and provide guidance to resolve quality... ...unlocking community knowledge in a new way. Experts add insights directly into each...Contract workTemporary workPart timeLocal areaImmediate startAfternoon shift$75.97k - $99.71k
...Overview Legend Biotech is seeking a QA Shop Floor Specialist II/III as part of the Quality... ...maintaining the highest standards in compliance within company policies, procedures,... ...manufacturing quality issues. Review of all documentation, in accordance with Good...Work experience placementImmediate startWorldwideFlexible hoursWeekend work- ...A leading document management firm is looking for a candidate in South Plainfield, NJ, to oversee document control processes and lead teams in improving document management functionalities. Candidates should possess a college degree, advanced knowledge of SharePoint,...
$81.27k - $106.67k
...multiple myeloma. Position QA Change Control Specialist II – Quality team, Raritan,... ...requirements in a sterile GMP environment. This role manages... ...controls, SOPs, and other documentation. Require minimal direction... ...assurance, manufacturing compliance, clinical quality, or cell...Permanent employmentContract workTemporary workWork experience placementWork at officeLocal areaWorldwideFlexible hoursShift work- Kashiv Biosciences LLC is seeking a Quality Assurance Specialist II in Piscataway, NJ. This full-time role involves supporting Quality Assurance... ...in reviewing and managing the quality system, ensuring compliance with cGMP requirements, and conducting quality audits. The...Full time
- The Quality Assurance Specialist will provide Quality oversight to... ...support Quality Reviews and QA Shop Floor manufacturing support... ...executed Batch Records, GMP documents and prepares documentation for... ...documents and ensure compliance to GMP. Documents to include...
- ...in Raritan, New Jersey, is hiring a QA Shop Floor Specialist. This role involves quality oversight... ...autologous CAR-T products, ensuring compliance within cGMP standards. The ideal... ...quality issues and ensuring proper documentation practices. The company offers comprehensive...
- ...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... ...manufacturing environment. Responsibilities include ensuring compliance with cGMP, supporting internal audits, and collaborating...
- Legend Biotech is seeking a QA Shop Floor Specialist as part of the Quality Operations team based... ...maintaining the highest standards in compliance within company policies, procedures,... ...quality issues. Review all documentation in accordance with Good Documentation...Permanent employmentFull timeFor contractorsLocal areaImmediate startFlexible hoursWeekend workDay shift
- A leading healthcare company is looking for a Quality Assurance Incoming Specialist II based in Raritan, NJ. The role involves overseeing the quality and compliance of materials for CAR-T production in a regulated environment. Candidates should have a Bachelor's degree...
$16.82 - $31.25 per hour
...Position Overview Dealership: L0397 Driveway Home Office Driveway.com | Document Compliance Specialist. The Specialist, Document Compliance is the key link between the Driveway Care Center and the Driveway customer for all paperwork processing. This senior customer service...Temporary workBank staffWork at officeHome officeShift work- A leading biotechnology firm in Raritan, New Jersey, is seeking a QA Document Control Specialist to support the document management process within its manufacturing facility. The ideal candidate will have a Bachelor's degree in a related field and at least 2 years of experience...
- ...Quality Assurance Specialist Lupin is comprised of a... ...lifecycle management of master documents by ensuring that all... .... Issuance of GMP documents i.e. logbooks... ...overall improvement of compliance. Support internal and... ...program. Management of QA retain samples and...Work at office
- ...experienced Quality Assurance Specialist to join our team. In... ...safety, integrity, and compliance of clinical trial... ...compliance with FDA, EU-GMP, GDP, ICH-GCP, DSCSA, and... ...JRS standards. The QA Specialist ensures that... ...and maintain controlled documents including SOPs, Work...Worldwide
- Join a forward-thinking company as a Quality Assurance Specialist, where you will oversee critical quality processes in a dynamic... ...environment. This role involves managing CMO oversight, ensuring compliance with GMP standards, and preparing for regulatory audits. You will...
- Sunrise Systems is seeking a Quality Assurance Specialist in Edison, NJ, to support cGMP quality operations. This hybrid role involves reviewing controlled documents, ensuring compliance with manufacturing practices, and supporting both clinical and commercial product releases...
- ...IT Quality Compliance Specialist/Analyst Hybrid role--Local Candidates Only Work... ...system validation for GMP, GDP, GLP space. Regulatory... ...deliverables, review and approval as a QA. Responsibilities: Manage... ...to cGxPs, guidance documents, applicable industry accepted...Local area
- ...Bristol Myers Squibb is looking for a contractor to support the Chemistry, Manufacturing, and Controls (CMC) documentation and specifications group. This role includes preparing and managing CMC content for regulatory submissions, collaborating with scientific teams, and...Hourly payFor contractors
$85k - $105k
...healthier through biotechnology. Job Title: Customs Trade Compliance Expert This position is based fully onsite in Piscataway, NJ. The... ...Permits. Interpret import/export regulations, rulings, and trade documentation. Conduct compliance audits to ensure full regulatory...- ...FOCO in Piscataway Township is seeking a Quality Assurance & Compliance Associate to support quality operations. This role involves ensuring products meet safety and compliance standards before shipment. The ideal candidate will have strong attention to detail and organizational...
$60k - $70k
...AML Compliance Specialist Job Category: Resorts World Bet Requisition Number: AMLCO002883 Posted: May 7, 2026 Full-Time Hybrid... ...activity. This includes reviewing customer profiles, account documentation, prior reviews, past investigations, and conducting online...Full timeShift work$93.46k - $122.67k
Job Overview QA Validation Specialist III role at BioSpace, based in Raritan, NJ... ...plant in a sterile GMP environment. Key Responsibilities... ...Responsibilities Provide quality and compliance oversight for computer... ...and validation documentation (specifications, protocols,...Work at officeFlexible hours- Supplier Compliance Specialist - Edison, NJ Compensation Range: $78,840 - $96,360. Possible Bonus:... ...detailed reviews, risk-based assessment of documentation, and request additional evidence or... ...compliance review process with QA; support follow-up actions and audit readiness...Work experience placementWork at office
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