QA Associate I: On‑the‑Floor cGMP & Documentation
PCI TRGR Penn Pharmaceutical Services Ltd
PCI TRGR Penn Pharmaceutical Services Ltd in San Diego is seeking a QA Associate I responsible for ensuring compliance with Quality Assurance (QA) requirements and maintaining a cGMP environment. The role involves documentation review, real-time QA oversight during manufacturing operations, and generation of cGMP labels. Ideal candidates possess a High School Diploma with a preference for a Bachelor's degree in Life Sciences, and relevant experience in QA or documentation. The position offers a competitive hourly rate and a full benefits package. #J-18808-Ljbffr PCI TRGR Penn Pharmaceutical Services Ltd
$21.69 - $24.41 per hour
The QA Associate I at PCI Pharma Services in San Diego is responsible for compliance with Quality Assurance requirements and collaborative team efforts. Duties include cGMP documentation review, area line clearance operations, and providing QA oversight during manufacturing...FloorHourly pay$21.69 - $24.41 per hour
SUMMARY The QA Associate I is responsible for performing a wide variety... .... The Associate I promotes a cGMP environment and collaborates... ...procedures. The Associate I performs documentation review and ensures... ...and performs real‑time, on‑the‑floor documentation review during manufacturing...FloorHourly payFull timeFlexible hoursAfternoon shift$100k - $118k
...while ensuring compliance with cGMP regulations, internal... ...shift. Perform Quality on the Floor (QOTF) activities to ensure compliance... ...manufacturing activities and documentation. Support batch record review... ..., logbooks, forms, and associated documentation as authorized....FloorShift workNight shift$24 - $45.5 per hour
...seeking a detail-oriented Quality Assurance (QA) Specialist to support operations in a... ...records, laboratory results, and quality documentation to ensure GMP compliance Support batch... ...Provide QA oversight on the manufacturing floor: Line clearance In-process checks Partner...FloorContract workTemporary work- PCI Pharma Services is seeking a QA Raw Materials reviewer to ensure cGMP compliance in routine QA activities. The role supports audits, training, and documentation review for GMP operations, while assisting with batch disposition and change control documentation. You will...SuggestedFull time
- ...protocols and work plans. May be assisted by QA Specialists and Sr. Specialists. Comply... ...production • Assist with packaging floor activities for primary and secondary (... ...production batch records, logbooks and other associated documents • Performs Quality verification of...FloorFull timeContract workImmediate start
- Artiva Biotherapeutics is seeking a Quality Assurance Operations professional to support document control, records management, and training administration in a GMP environment. You will oversee controlled documents, training records, labeling activities, and related quality...
- Artiva Biotherapeutics Inc. is hiring for a Quality Assurance Operations role focused on document control, training management, and controlled labeling in our eQMS. You will ensure documents, training records, labeling, logbooks, and related quality records are accurate...For contractors
- ...most. We are seeking a Quality Assurance Associate II to join our team. This role is... ...production activities, ensuring compliance with cGMP and regulatory standards. The position... ...issuance, and management of controlled documentation across GLP/GCP/GMP systems. The ideal candidate...Work at office
$30 - $33 per hour
...re looking for a Senior Quality Assurance Associate who enjoys being close to the product,... ...Management System to complete tasks related to document control, training systems, change... ...top of mind. What You’ll Do As a Senior QA Associate, you’ll play a critical role in...Hourly payLocal area$72k - $74k
...-formulation testing, formulation and analytical development, cGMP manufacturing and clinical packaging, labeling, and worldwide... ...throughout the product lifecycle. This involves ensuring that all documentation is accurate, up-to-date, and properly maintained in accordance...Contract workWork experience placementLocal areaWorldwideMonday to Friday$85k - $89k
...compliance with regulatory requirements, good manufacturing practices (cGMP), and standard operating procedures. Responsible for... ...pre- and post‑execution batch record review. Author and update documents related to material management quality control, batch records,...Contract work- ...The Document Control Team is a key element of the Quality Assurance department and is responsible... ...to job role(s) and performance of associated activities in compliance with SOPs.... ...communicate across various employee levels (i.e. floor level, mid and upper management)...FloorContract workWork at office
- ...Therapeutics is seeking a Quality Assurance Associate II to support batch record review, deviations, and controlled documentation in a cGMP environment. The role involves document... ...training records, and collaboration with the QA team to ensure regulatory readiness. The...
$75k - $85k
...in patient lives. The Quality Assurance QA Associate II - Quality Events Team (QET) is... ...preventive actions (CAPAs) in compliance with cGMP, SOPs, and regulatory requirements.... ...of quality events. Track and maintain documentation of deviations and CAPAs in compliance with...Work at officeRemote work$65k - $70k
Catalent, Inc. in San Diego is hiring a Quality Assurance Associate I, Analytical to ensure compliance with quality standards. The position... ...with HPLC. The successful candidate will review controlled documents and support various manufacturing activities while enjoying...- ...on broad technical skills and QA experience, anticipates and identifies... ...good manufacturing practices (cGMP) and standard operating... ...tested and released Performs document generation and review... ...based approach Support functions associated with the packaging of clinical...
- ...Sciences and at least 3-5 years of relevant experience in quality assurance. The role involves generating and reviewing critical documentation, fostering a compliant environment, and promoting safety protocols. The hiring rate is competitive, including benefits such as...
$25 - $31 per hour
...Exempt Non-Exempt Summary It is the responsibility of the Quality Assurance Specialist to assemble assigned departmental reports and documentation related to quality management and performance improvement activities within the Centers for Disease Control, any State, and...Remote workShift work- ...requirements, and verify usage and effectiveness of required and/or authorized facilities, equipment, and tooling. You will review work documents prior to release, and upon completion of work to verify all processing and documentation requirements have been fully executed....
$89.22k - $122.67k
...25. Experience in interpreting regulatory policies and guidance documents and can correctly apply them as appropriate to related activities... ...results on time. Willing to travel 10% - 25%. Relevant QA experience for 3-5 years in a 21 CFR Part 211 or 212 regulated industry...Temporary workLocal area- ...Assurance through AI-enabled knowledge systems. We are seeking a QA Specialist to support and strengthen our GxP quality framework... ...ll Do Own and maintain GMP / GxP SOPs, policies, and controlled documents across QA, QC, Manufacturing, and Clinical operations. Use PDAOAI...
- ...is performed in compliance with regulatory requirements and company policies Assisting in the preparation and review of study documents Participating in quality assurance audits and inspections Collaborating with cross-functional teams to ensure project milestones...Temporary workWork at officeShift work
$27 - $33 per hour
...improving care Own our roles, staying accountable for outcomes and documenting accurately Build genuine connections with members, families,... ...Health (BH), and Community Health Worker (CHW) operations. The QA Specialist serves as the internal auditor, workflow analyst,...Hourly payFull timeTemporary workFlexible hours$85k - $89k
...of small molecule and peptide drug candidates. Responsibilities Pre- and post-execution batch record review Authoring and updating documents related to Material Management Quality Control, Material Management Quality Assurance, Batch Records, Compliance, and Validation...Monday to Friday$60k - $85k
...Description Support Quality Assurance (QA) Batch Record Review, Product Disposition... ...party contract organizations to resolve any documentation discrepancies identified during review.... ...location is between $60,000-$85,000 for Associate level. The final wage offered to a...Contract work- ...Diverzify+! We are the largest and most respected commercial flooring installation service company in the industry, with 60+ locations... ...team to handle change orders, billings, and close-out documentation. High School Diploma/GED Previous sales experience as an...FloorContract workFor contractors
$19 - $26.5 per hour
BioLegend is seeking an Associate for their Quality Control group in San Diego, California. The candidate will be responsible for testing high quality reagents, including antibodies and proteins, utilizing techniques such as flow cytometry, immunohistochemistry, and ELISA...Hourly pay- R&D Partners is seeking to hire a QA Complaint Intake Specialist in San Diego, CA . Your main responsibilities as a QA Complaint... ...channels. Review incoming complaint information and supporting documentation to assess reported events, identify potential complaint...
- ...candidate will possess a Bachelor's degree in a related field, with at least two years of relevant experience. You will play a vital role in continuous improvement efforts while upholding high standards of documentation and member care. #J-18808-Ljbffr Pacific Health Group
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