On-Site GMP Quality Assurance Associate (Contract)
Medvacon Life Sciences, LLC
Medvacon Life Sciences, LLC is looking for a Quality Assurance Associate in San Diego, California. This on-site contract position lasts for 3 months with a potential for extension. Responsibilities include inspecting materials for GMP production and ensuring compliance with FDA guidelines. The ideal candidate will have an Associate's degree, excellent communication skills, and the ability to work effectively under pressure. Join us in our mission to maintain high-quality standards in clinical supplies. #J-18808-Ljbffr
- ...Sonara Inc. is seeking a Quality Associate for an on-site contract opportunity in San Diego, California. The successful candidate will inspect incoming materials for GMP production and assist with various packaging activities, ensuring compliance with FDA guidelines....Contract workWebsite
$75k - $83k
...Sr. Quality Assurance Specialist Location: San Diego, CA |... ...key quality activities associated with cGMP manufacturing... ...and interact with contract testing laboratories.... ...authority. Ensure site adherence to Quality System... ...competencies include: GMP compliance and...Contract workWebsiteFull timeCasual workWork at officeWorldwideAfternoon shift$85k - $89k
Quality Assurance Specialist II - San Diego By Catalent, Inc., a leading global contract development and manufacturing organization (CDMO), this 100% on‑site position focuses on early‑stage development of small molecule... ...change actions. Adhere to GMP standards routinely with...Contract workWebsite$85k - $89k
Catalent Pharma Solutions is looking for a Quality Assurance Specialist II in San Diego. This role supports clinical trial projects with essential... ...review, document authoring, and ensuring compliance with GMP standards. Applicants should have a high school diploma or GED...Website$85k - $89k
Catalent in San Diego is hiring a Quality Assurance Specialist II responsible for ensuring regulatory... .... Candidates should have relevant GMP experience and educational qualifications... ...standards. The position is full-time, on-site with a competitive salary range of $85,0...WebsiteFull time- ...entry-level Document Control Associate in San Diego, CA. The role involves... ...control processes related to GMP and GDP, overseeing the... ...and ensuring compliance with site procedures. Successful candidates... ...processes. This position is a contract role requiring candidates to be...Contract workWebsiteMonday to Friday
- ...Control (Mu st Have GMP/GDP and Document Control... ...Level Employment Type: Contract on W2 (Need US Citizens... ...Job Description: Associate will oversee document management... ...and reviewed by quality. Scanning of documents... ...by Quality per site procedures. Associate...Contract workWebsiteMonday to FridayFlexible hoursDay shift
$94.78k - $128.23k
...Classification On-Site Job Function Quality Company Overview... ...Follows and/ or develops, assures and maintains the quality... ...education and experience: Associate's Degree and 5-7 years' experience... ...an employment agreement or contract, implied or otherwise.Contract workWebsiteFull timeTemporary workWork at officeShift work$65k - $70k
Quality Assurance Associate I, Analytical Catalent, Inc. is a leading global contract development and manufacturing organization (CDMO) dedicated to delivering unparalleled service... ...testing, formulation development, GMP manufacturing, and stability storage and testing...Contract work- ...knowledge and experience 10+ years Quality Assurance experience in a GMP manufacturing environment or equivalent... .... Participates in and maintains site audit readiness by working closely with... ...-based approach Support functions associated with the packaging of clinical and...Website
$22.5 - $24 per hour
...supervision and according to Quality Test Procedures (QTP) & Standard... .../Sat/Sun 5am - 530pm pst on-site.)Performs In-process, Final Inspection... ...History Records (DHRs), associated test reports and records and... ...methods and general knowledge of GMP requirements for production....WebsiteHourly payLocal areaWork visaFlexible hoursShift workWeekend work- ...Job Description This is an on-site contract opportunity. 3 months with potential... ...inspection of incoming materials for GMP production • Assist with packaging... ...batch records, logbooks and other associated documents • Performs Quality verification of just-in-time labeling...Contract workWebsiteImmediate start
$90k - $110k
The Quality Systems Specialist III is responsible for enhancing the Quality Management System (QMS) to ensure compliance with... ...requirements. Candidates must have a background in Quality Assurance within a GMP regulated environment and will be expected to drive key Quality...Contract workTemporary work$130k - $153k
...External Quality Operation Manager (GMP) Full-time Sobi Location: United States Statistics show that women and underrepresented groups tend to apply... ...of contact for all quality-related activities at the Contract Manufacturing Organization (CMO) Ensure that all aspects...Contract workWebsiteFull timeTemporary workWorldwide- ...company development, including contract research in low-Earth orbit.... ...Under supervision, the QC Associate will focus on QC activities supporting... ...of analysis, and managing off-site testing of QC samples. Will... ...Good Manufacturing Practice (GMP), Food and Drug Administration...Contract workWebsiteHourly pay
$140k - $150k
...validating the Guaranteed Maximum Price (GMP). This role functions as both a technical... ...bid packages aligned with project scope and contract requirements. You will coordinate all aspects... ...of project scheduling, sequencing, and site logistics as they relate to costs Proficiency...Contract workWebsiteFor contractorsFor subcontractorLocal area$33 per hour
...Specialists. Comply with divisional and site Environmental Health and Safety... ...inspection of incoming materials for GMP production Assist with packaging... ...batch records, logbooks and other associated documents Performs Quality verification of just-in-time labeling...WebsiteHourly payFull timeLocal areaFlexible hours- Peregrine Team is seeking a Quality Assurance Specialist in San Diego to support a growing biotech organization. You will review batch records... ...holds a Bachelor’s degree and has 3-5+ years of experience in a GMP-regulated environment, with strong knowledge of FDA...
$70.3k - $75.93k
PCI TRGR Penn Pharmaceutical Services Ltd is hiring a Quality Assurance Specialist based in San Diego, California. This role supports clinical trial and operations activities, ensuring compliance with GMP and company procedures while performing product inspections, document...$34.29 - $61.02 per hour
Quality Control Associate (#139933) Apply Deadline: Fri 6/12/2026. Job Details Title... ...Percent: 100% Union: RP Contract Total Openings: 1 Work... ...analysis, and managing off‑site testing of QC samples. The role... ...Good Manufacturing Practice (GMP), Food and Drug Administration...Contract workWebsiteHourly payMonday to FridayDay shift$85k - $89k
Position Summary Quality Assurance Specialist II - supports clinical trial projects through quality... ..., core hours 8:00am-4:30pm, 100% on-site (San Diego). This position is part of Catalent... ...controls and action plans Adhere to GMP standards with limited errors and guidance...WebsiteMonday to Friday$89.22k - $122.67k
...next step in their career. As a Quality Specialist, you will be... ...Quality oversight of a US based site that manufactures and distributes... ...Healthineers Radiopharma. Focusing on GMP Investigations and CAPA’s,... ...Are an expert in the quality assurance disciplines of problem‑solving...WebsiteTemporary workLocal area- ...design phases and setting the GMP and establishing the projects... ...maintaining and enforcing project site safety programs Make... ...to the project team to ensure quality control remains a priority throughout... ...PlanGrid to organize all contract documents and progress photo documentation...Contract workWebsiteFor subcontractor
- Siemens Healthineers is seeking a Quality Specialist in San Diego, CA, responsible for providing quality oversight for the... ...sterile drug manufacturing, regulatory compliance, and quality assurance. You will manage GMP investigations, conduct audits, and participate in...
- ...Planet Pharma Group is seeking a QA Associate in San Diego, CA. The role includes inspecting incoming materials for GMP production, reviewing production batch records, and... ...excellent communication skills, and adherence to quality control standards. Physical demands include...
$220k - $260k
...management of the proposal to assure they align with the... ...Enforces safety on job site and implements, enforces... ...Extensive knowledge of Prime Contract and contract types including lump sum, GMP, hard bid, negotiated,... .... Strategic decision quality and use of sound judgement...Contract workWebsitePermanent employmentTemporary workFor contractorsWork experience placementLocal area$26.85 - $28.85 per hour
...Technician Location: San Diego CA Duration: 6 Months (Contract to hire) Pay Range: $26.85 - $28.85 per hour on W2... ...proper integration with design intent. Resides at project sites to support commissioning and client coordination activities....Contract workWebsiteHourly payFor contractorsFor subcontractor- CSV Quality Specialist (On‑Site - San Diego, CA) Join a collaborative QA team at a clinical‑stage biopharmaceutical... ...and gene therapies. In this on‑site contract role, you’ll lead and enhance the... ...background with experience in GMP systems. Proficiency with QMS tools (Change...Contract workWebsite
$110k - $150k
...estimating, procurement, and scheduling. Develop and maintain site logistics plan, in coordination with Project Manager. Assist... ...relating to cost and schedule. Exhibit thorough knowledge of contract documents, project requirements, and 3rd party agreements including...Contract workWebsiteTemporary workFor contractorsFor subcontractor- ...seeking a Senior Data Integrity Consultant in San Diego, California, for a long-term contract. The role supports Data Integrity and Computer System Validation activities within a GMP-regulated biotech environment, ensuring compliance with FDA and EU regulations. The ideal...Long term contract
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