Quality Control Associate II GMP Biotech QC
$75k - $87kCapricor Therapeutics, Inc.
A biotechnology company in San Diego is seeking a laboratory professional to support quality control (QC) analytical assays. The ideal candidate will have a Bachelor's in Biological Sciences and at least 2 years of experience in 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 science and innovative therapies. #J-18808-Ljbffr
$75k - $87k
...and families who need them most. The Quality Control Associate II, Controls will support the development,... ...analytical control materials used in QC assays. This role will be responsible for... ...document findings in accordance with GMP and data integrity requirements. Document...Suggested$29 - $39 per hour
...Job Description Job Description Quality Assurance Specialist II - Simply Biotech OVERVIEW Are you looking for... ...Assurance Experience - 3+ yrs. GMP level Audits/CDMO a +/pharma or... ...closely with Production, Quality Control, and other departments to address...SuggestedWork at officeImmediate start$23.55 - $31.5 per hour
...Job Summary At 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...SuggestedFull timeTemporary workPart timeWork experience placement$70k - $87k
...most. Position Summary The Quality Control Associate, Raw Materials is... ...regulatory requirements, and GMP standards. As part of the QC Raw Materials team, you will... ...or industry). Associate II: 1+ years of QC experience... ...environment (pharma, biotech, or manufacturing). Strong...SuggestedWork at office$70k - $82k
...individual to join our Quality Compliance department.... ...candidate brings hands‑on GMP/GxP auditing experience... ...g., GMP manufacturing, QC, validation,... ...experience within biopharma, biotech, medical devices, or related... ..., CAPA, Change Control, Training, Document Control...Suggested$34.29 - $61.02 per hour
...Quality Control Associate (#139933) Apply Deadline: Fri 6/12/2026. Job... ...Under supervision, the QC Associate will focus... ...in a pharmaceutical, biotech, drug manufacturing, or... ...Manufacturing Practice (GMP), Food and Drug... ...work in Biosafety Level II environment where biological...Hourly payContract workMonday to FridayDay shift- ...Description Under supervision, the QC Associate will focus on QC activities... ...in a pharmaceutical, biotech, drug manufacturing, or academic... ...Good Manufacturing Practice (GMP), Food and Drug Administration... ...Willingness to work in Biosafety Level II environment where biological (...Hourly pay
- ...and families who need them most. We are seeking a Quality Assurance Associate II to join our team. This role is critical in... ...investigations, label issuance, and management of controlled documentation across GLP/GCP/GMP systems. The ideal candidate is detail-oriented,...Work at office
- ...Therapeutics, Inc. in San Diego, California, is seeking a Quality Assurance Associate II. This critical role supports clinical production... ...batch record review, deviation investigations, and managing controlled documentation. Candidates with 0-3 years of experience in...
- Peregrine Team is seeking a Quality Assurance Specialist in San Diego to support a growing biotech organization. You will review batch records, support audits, and ensure... ...’s degree and has 3-5+ years of experience in a GMP-regulated environment, with strong knowledge of...
$120k - $150k
...than 7,000 strong. Overview The Senior Quality Systems (QS) Specialist II is responsible for leading the... ...Management System (QMS) in alignment with GMP, FDA, ISO, and global regulatory requirements... .... Strong understanding of change control requirements. Strong understanding of...Work at officeWorldwide$75k - $95k
The Quality Control Associate III, Sample Management is responsible for the receipt, tracking, storage, distribution, and disposal of samples in a... ...Familiarity with LIMS or electronic tracking systems Knowledge of GMP/GLP regulations Skills and Competencies Strong attention...$22.5 - $24 per hour
...slim X2 insulin pump with Control-IQ+ technology — an... ...supervision and according to Quality Test Procedures (QTP) &... ...History Records (DHRs), associated test reports and records... ...with QSRs, QC testing methods and general knowledge of GMP requirements for production...Hourly payLocal areaWork visaFlexible hoursShift workWeekend work$100k - $118k
...graveyard) shift role supporting off-hours GMP manufacturing. As a Quality Assurance Specialist at Capricor,... ...records, logbooks, forms, and associated documentation as authorized. Identify... ...Support investigations, CAPAs, change controls, and quality risk assessments as...Shift workNight shift- ...Peregrine Team is hiring a Quality Assurance Specialist to support a growing biotech organization focused on developing and... ...records, deviations, and change controls in accordance with cGMP guidelines... ...~3–5+ years of experience in a GMP-regulated environment (biotech/pharma...Full time
- ...and Safety requirements. II. Essential Functions: •... ...of incoming materials for GMP production • Assist with... ..., logbooks and other associated documents • Performs Quality verification of just-in-time... ...programs, procedures and controls to ensure that products conform...Contract workImmediate start
- ...USLA BioLegend, Inc. is seeking a Quality Control Associate I for Flow Cytometry on the PM Shift in San Diego. The role involves testing high-quality reagents while following SOPs and ISO requirements. Candidates should be motivated science enthusiasts ready to work in...Shift work
$19 - $26.5 per hour
...Job Title Quality Control Associate I, Flow Cytometry (PM Shift) Location San Diego About Us Revvity is a developer and provider of end-to-end solutions designed to help scientists, researchers, and clinicians solve the world’s greatest health challenges. We pair the enthusiasm...Hourly payFull timeWork experience placementLocal areaShift work- 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
$23 - $35 per hour
...Now Hiring Quality Associate Location: San Diego, CA Pay Rate: $23.00 $35.00 per hour (based on experience) 2nd Shift: 2:30 PM 11:00 PM... ...manufacturing environment 3+ years of experience in quality control, performing visual and mechanical inspections 3+ years of experience...Hourly payContract workFor contractorsLocal areaImmediate startShift workAfternoon shift- Actalent is seeking a 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...
$29.65 - $33.36 per hour
...PCI TRGR Penn Pharmaceutical Services Ltd is seeking a Quality Assurance professional in San Diego, California. This position involves... ...requirements, assisting with audits, and providing quality support for GMP operations. Ideal candidates will have a Bachelor’s degree in...Hourly pay- ...Medvacon Life Sciences, LLC is looking for a Quality Assurance Associate in San Diego, California. This on-site contract position lasts for 3 months... .... Responsibilities include inspecting materials for GMP production and ensuring compliance with FDA guidelines. The...Contract work
- ...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...
$33 per hour
...Adecco is hiring immediately for a Quality Assurance Associate with a local client in San Diego, CA... ...of quality-related tasks in support of GMP production. This role involves routine... ...labeling processes · Manage document control activities, including issuance, scanning...Hourly payTemporary workLocal areaImmediate startShift work- ...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 work
$33 per hour
...inspection of incoming materials for GMP production Assist with... ...batch records, logbooks and other associated documents Performs Quality verification of just-in-time labeling... ...in Quality programs, procedures and controls to ensure that products conform to...Hourly payFull timeLocal areaFlexible hours- ...who need them most. The QC Specialist, Analytical supports the quality and compliance of cell... ...Contribute to change control activities and assess potential... ...complete, and compliant GMP documentation in alignment... ...related function within biotech or pharmaceutical industry...Work at officeShift work
- ...with Precision Diagnostics ® We are looking to add a Quality Control Laboratory Associate I . The QC Lab Associate I is responsible for ensuring that only... ...regulations and industry standards, and to maintain GMP environment. The Quality Control Laboratory Associate...InternshipWork at officeWorldwide
- Actalent is seeking a detail-oriented Quality Assurance Specialist to support operations in a GMP-regulated pharmaceutical manufacturing environment in San Diego... ...include reviewing production records and performing document control activities. #J-18808-Ljbffr Actalent
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