QA Associate Specialist GMP & FDA Compliance
$65.99k - $90.74kShiseido
Shiseido is seeking a Quality Assurance Associate Specialist in East Windsor Township, NJ. This role focuses on ensuring FDA compliance, reviewing GMP documentation, and releasing Finished Goods. The ideal candidate has a bachelor's degree in Engineering or Science and at least two years of quality assurance experience in the pharmaceutical sector. You will prepare the CARESS ACT list, conduct quality training, and manage batch records. A salary range of $65,992 to $90,739 per year is offered. #J-18808-Ljbffr
$52k - $70k
...sample inspections and control finished product and raw material retain samples stored in the reserve sample room. • Monitor GMP areas for compliance with general GMP requirements such as proper gowning and cleanliness, per CFR21 Subpart A General Provisions to assure...Suggested- ...and process changes/deviations before product release to ensure compliance with defined specifications. This includes addressing and... ...food, or chemical industriesKnowledge of ISO 9001 and HACCP and GMP standardsProficiency in Microsoft Office and quality systems (e...SuggestedWork at office
- ...LifeSciencesPosted: 2026-08-19INTEGRA LIFESCIENCES CORP is seeking a Lead Auditor for Quality Compliance to oversee corporate audits across multiple facilities. The role demands extensive GMP auditing experience and the ability to evaluate quality management systems within...Suggested
- ...supervision, the Quality Assurance Specialist III will ensure systems and processes are in a state of compliance with regard to internal,... ...training records, and other ISO/GMP-related items, as needed to... ...understanding of laboratory regulations (FDA, ISO, GLP, GMP). Experience...SuggestedFull timeContract workFor subcontractorMonday to Friday
- ...documents. Provide guidance and training to other QA staff in quality assurance activities.... ...-5 years of QA/validation experience in an FDA-regulated industry. • Familiarity with... ...manufacturing processes and thorough understanding of GMP. • Strong technical writing skills and the...Suggested
- ...Quality Assurance Specialist Integrated Resources, Inc., is led by... ...include new test methods Ensure compliance with all company policies and... ...regulations, including FDA and ISO 9001, ISO 13485, CMDR... ...with third part labs Maintain GMP/GLP laboratory notebooks and documentation...Work at office
- ...Quality Assurance Documentation Specialist This position provides... ...and invoices. The role assists QA product managers with responsibilities... .... Review Status Updates to FDA. Perform additional duties as... ...~3+ years of experience in a GMP environment such as a Pharmaceutical...For contractors
$79k - $127.65k
...their merit.Job Function: QualityJob Sub Function: Quality & Compliance AuditJob Category:ProfessionalAll Job Posting Locations:... ...at are searching for the best talent for Pharmacovigilance QA Auditor Specialist to be located at Raritan, NJ; Titusville, NJ or Horsham, PA...Full timeWork experience placementWork at officeLocal areaImmediate start- ...Quality Assurance Specialist Monroe Township, New Jersey... ...- Support daily QA operations related to document... ..., and deviations in compliance with internal procedures... ...Quality Systems within a GMP or ISO 13485regulated... ...Knowledge of ISO 13485, FDA QSR, and GMP...Work at office
$26 - $30 per hour
...Job Title: Quality Assurance Specialist Location: Princeton, NJ Work Model: Onsite... ...deviations before product release to ensure compliance with defined specifications. This... ...Knowledge of ISO 9001 and HACCP and GMP standards Proficiency in Microsoft Office...Full timeContract workWork at officeLocal areaDay shift- WuXi Biologics is seeking a Senior QA Specialist I located in Cranbury Township, NJ, to handle quality assurance activities related to Drug... ...the ability to perform critical tasks related to process compliance and regulatory adherence. The role requires extensive QA activities...
$60.2k - $96.3k
Job Title - Quality Control Specialist (Weekend) Work Location - Cranbury... ..., report generation and GMP documentation. Job Responsibilities... ...according to and in compliance with cGMP guidelines and internal... ...requirement including cGMP, ICH, EMA, FDA, and other global compendia...Work experience placementImmediate startShift workNight shiftWeekend work$63k - $93k
...hiring a Quality Assurance Documentation Specialist- Supplier Quality in our Cranbury, NJ location... .... They have a solid working knowledge of FDA regulations, FSMA, and GFSI standards,... ...and Abilities Familiar with GFSI or NSF QA Standards and Auditing systems FSMA requirements...Work at officeLocal areaRemote work- ...Responsible for assigned operational Quality Risk and Compliance (QRC) activities supporting Research and Development (R&D) quality efforts, including inspection readiness (IR), process improvement, training, and other assigned duties. This role works closely with Quality...Temporary workWork at office
- ...motivated Submarine Systems Quality Assurance Specialist to join our team in Philadelphia, PA... ...Quality Evidence (OQE) to verify compliance with contract, drawing, and performance... ..., or electromagnetic systems and associated equipment. EDUCATION: ~ Bachelor...Contract work
$103.95k - $240.35k
...is seeking Quality Assurance Specialists to join our team, providing professional... ...methodologies to ensure compliance with standards and procedures... ...hardware, software, and associated documentation, participating... ...Performance Indicators (KPIs). Perform QA activities to validate...Permanent employmentFull timeContract workPart timeWork experience placementLocal areaRemote work- ...Quality Control Specialist Monroe Township, New Jersey, United States About the Job Quality... ...Control or Quality Assurance within a GMP-regulated manufacturing environment. -... ...Working knowledge of ISO 13485, GMP, and FDA quality regulations is a plus. - Strong attention...Work at office
- ...Digital Dog Direct is currently searching for a Quality Assurance Associate with experience in the print & mail industry. This full-time... ...Responsibilities: Under the direction of the Production and Compliance Manager, the Quality Assurance Associate is responsible for...Full time
- Overview It’s a mix of relationship-building, problem-solving, and attention to detail—way more than just a typical sales role! It’s about understanding. It’s a mix of relationship-building, problem-solving, and attention to detail—way more than just a typical sales role...
$20 - $29 per hour
...is supporting the Pharmaceuticals organization and has an opening for a Quality Specialist in Princeton, NJ (50% Hybrid). Position Summary: We are seeking a Quality Risk & Compliance (QRC) Specialist to support Research & Development (R&D) quality initiatives,...Hourly payContract workLocal areaRemote work$77.9k - $104.37k
...succeeds. Responsibilities: Conduct quarterly file audits for all lines of business against business process flows to determine compliance with regulatory standards according to NCQA, URAC and CMS. Analyze, prepare, and distribute quarterly audit outcomes including error...Full timeWork experience placementLive inLocal areaRemote work- Job Description Day to Day: The Supplier Quality Specialist is responsible for supporting the supplier quality program through the review... ...and verified, and supplier quality records are maintained in compliance with regulatory and corporate quality standards. The role...
- ...Quality Assurance Auditor to join our Monmouth Junction, NJ facility. The role focuses on auditing DC output, ensuring order compliance, and supporting QA processes. You will contribute to non-conformity resolution, training, and continuous improvement while working onsite...
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