QA Associate II - GMP/GLP Compliance
Capricor Therapeutics, Inc.
Capricor Therapeutics, Inc. in San Diego, California, is seeking a Quality Assurance Associate II. This critical role supports clinical production activities while ensuring compliance with cGMP and regulatory standards. The ideal candidate should hold a Bachelor’s degree in a relevant field and possess strong organizational skills. Responsibilities include batch record review, deviation investigations, and managing controlled documentation. Candidates with 0-3 years of experience in a regulated environment are encouraged to apply. #J-18808-Ljbffr
$29.65 - $33.36 per hour
...Assurance professional in San Diego, California. This position involves ensuring compliance with quality assurance and regulatory requirements, assisting with audits, and providing quality support for GMP operations. Ideal candidates will have a Bachelor’s degree in Life...SuggestedHourly pay- ...most. We are seeking a Quality Assurance Associate II to join our team. This role is critical... ...production activities, ensuring compliance with cGMP and regulatory standards. The... ...management of controlled documentation across GLP/GCP/GMP systems. The ideal candidate is detail-...SuggestedWork at office
$21.69 - $24.41 per hour
...PCI TRGR Penn Pharmaceutical Services Ltd in San Diego, CA, is hiring a QA Associate I to ensure compliance with Quality Assurance requirements. This role involves reviewing documentation, supporting quality investigations, and conducting inspections. The ideal candidate...SuggestedHourly pay- ...biotech organization. You will review batch records, support audits, and ensure compliance with cGMP guidelines. The ideal candidate holds a Bachelor’s degree and has 3-5+ years of experience in a GMP-regulated environment, with strong knowledge of FDA regulations. This role...Suggested
- ...Tandem Diabetes Care, Inc. is looking for a Quality Assurance Associate II in San Diego, California. This role involves conducting in-process and final inspections of manufacturing goods, ensuring compliance with FDA regulations, and maintaining detailed documentation....Suggested
$65k - $70k
...Catalent, Inc. in San Diego is hiring a Quality Assurance Associate I, Analytical to ensure compliance with quality standards. The position demands a Bachelor's degree in a relevant field and at least one year of GMP experience, preferably with HPLC. The successful...- ...Sonara Inc. is seeking a Quality Associate for an on-site contract opportunity in San Diego, California... ...will inspect incoming materials for GMP production and assist with various packaging activities, ensuring compliance with FDA guidelines. Applicants must hold an...Contract work
$75k - $87k
...laboratory environments. Responsibilities include executing assays, maintaining control materials, and documenting laboratory work in compliance with GMP. The position offers a salary range of $75,000 - $87,000 annually, reflecting the company's commitment to advancing medical...$29 - $39 per hour
...Description Quality Assurance Specialist II - Simply Biotech OVERVIEW Are you looking... ...Quality Assurance Experience - 3+ yrs. GMP level Audits/CDMO a +/pharma or biotech... ...Specialist II supports quality and compliance activities within a regulated manufacturing...Work at officeImmediate start- ...Quality Systems Specialist in San Diego, CA to support quality assurance operations in a GMP-regulated pharmaceutical environment. This role involves reviewing batch records, compliance documentation, and supporting production activities to ensure quality standards are...
$70k - $82k
...seeking an individual to join our Quality Compliance department. This role conducts internal and... .... The ideal candidate brings hands‑on GMP/GxP auditing experience within the life sciences... ...reasonable improvements. Collaborate with QA/QC, Manufacturing, Regulatory, Supply...$22.5 - $24 per hour
...manufacturing Design History Records (DHRs), associated test reports and records and reports... ...Verifies training and other records for compliance to specifications.Assists with resolving... ...methods and general knowledge of GMP requirements for production.Experience with...Hourly payLocal areaWork visaFlexible hoursShift workWeekend work- ...oriented Quality Assurance Specialist to support operations in a GMP-regulated pharmaceutical manufacturing environment in San Diego,... ...production setting. The ideal candidate will have a Bachelor's degree and QA experience in a GMP environment. Responsibilities include...
- ACADIA Pharmaceuticals Inc. is seeking an Associate Director, Quality Operations in San Diego, CA. This critical role ensures the quality and compliance of clinical and commercial products, overseeing GMP quality for internal operations and CMOs. The ideal candidate should...Work at office3 days per week
$75k - $87k
...patients and families who need them most. The Quality Control Associate II, Controls will support the development, qualification, and... ...data, summarize results, and document findings in accordance with GMP and data integrity requirements. Document all laboratory work...$120k - $150k
...The Senior Quality Systems (QS) Specialist II is responsible for leading the planning,... ...Management System (QMS) in alignment with GMP, FDA, ISO, and global regulatory requirements... ...complex quality system processes, leads compliance improvement initiatives, mentors other specialists...Work at officeWorldwide- ...plans. May be assisted by QA Specialists and Sr.... ...Safety requirements. II. Essential Functions:... ...incoming materials for GMP production • Assist with... ...approval, facility compliance, auditing, label inspection... ..., logbooks and other associated documents • Performs...Contract workImmediate start
$43.1k - $61.6k
...flexibility, learning, and career development. Summary Under minimal supervision, the Dental QA Associate supports quality assurance activities related to dental claims review, compliance, and process accuracy. This role requires strong dental knowledge, attention to detail,...Full timeWork at officeFlexible hours- ...Gainwell Technologies LLC is seeking a Dental QA Associate in California to support quality assurance activities related to dental claims review. You will ensure compliance, analyze clinical documentation, and report on quality evaluations. The ideal candidate will have...
- ...and Specialty Services (CSS) Quality Assurance Specialist I supports clinical trial projects, ensuring all work is performed in compliance with regulatory requirements and company policies. Location: 8926 Ware Court, San Diego, CA 92121 Onsite Position: Shift - Mon...Temporary workWork at officeShift work
$30 - $33 per hour
...Diagnostics in San Diego is seeking a Senior Quality Assurance Associate to contribute significantly to product quality and regulatory compliance. In this hands-on role, the successful candidate will perform QA release processes, review Device History Records (DHRs), and...Hourly pay$33 per hour
...work plans. May be assisted by QA Specialists and Sr.... ...inspection of incoming materials for GMP production Assist with packaging... .../room approval, facility compliance, auditing, label inspection,... ...records, logbooks and other associated documents Performs Quality...Hourly payFull timeLocal areaFlexible hours$23.55 - $31.5 per hour
...BioLegend we are dedicated to commercializing high quality reagents to support the research community for legendary discoveries. The QC Associate II for BioLegend’s Quality Control group will test products such as antibodies and proteins in the following applications: flow...Full timeTemporary workPart timeWork experience placement$70.3k - $75.93k
PCI Pharma Services is looking for a Quality Assurance Specialist in California to support clinical trial packaging, inspection, and quality metrics tracking. The role requires a High School Diploma and 3-5 years of relevant experience. Responsibilities include document...- ...Artiva Biotherapeutics is seeking a Quality Assurance professional responsible for compliance activities supporting deviations, CAPAs, change control, and product releases. The ideal candidate has over 5 years of experience in an FDA regulated industry and a Bachelor’...
- ...Artiva Biotherapeutics Inc., based in San Diego, California, is looking for a Quality Assurance Compliance professional. This role is focused on supporting deviations, CAPAs, and change control processes critical for ensuring compliance in a regulated industry. The ideal...
- ...Inc. is seeking a skilled quality management professional in San Diego, California. This role involves managing quality systems compliance, drafting regulatory documents, and supporting audits. The candidate should excel in technical writing and possess a strong regulatory...
$90k - $110k
...coordination, and improvement of the Quality Management System to ensure compliance with FDA and ISO standards. Candidates should have a Bachelor’s... ...years of relevant experience in Quality Assurance within a GMP environment. The salary ranges from $90,000 to $110,000, based...Temporary work- ...maintains necessary regulatory approvals. The role includes managing documentation, compliance operations, and communication with regulatory agencies. Ideal candidates will possess an Associate's degree, be bilingual in English and Spanish, and demonstrate good...
$70.3k - $75.93k
...duties may be assigned. #Perform product lot disposition by reviewing executed packaging records for completeness, accuracy, and compliance to GMP and company procedures. #Perform document change control activities as needed. #Perform and lead in investigations,...Full timeFlexible hours
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