Onsite QA Associate - GMP & Continuous Improvement
Regulatory Jobs
Amgen in Thousand Oaks, CA seeks an Associate Quality Assurance to sample and inspect raw materials and components, manage documentation, and lead small improvement projects. The role is fully onsite, expects ability to lift 30+ pounds, pass a vision assessment, and work in clean room sampling areas. Training on GMP will be provided; prior GMP is a plus. Qualifications include high school diploma with 2 years QA experience or an Associate's + 6 months, or a Bachelor’s degree. #J-18808-Ljbffr Regulatory Jobs
Vacancy posted 2 days ago
Similar jobs that could be interesting for youBased on the Onsite QA Associate - GMP & Continuous Improvement in Thousand Oaks, CA vacancy
- Amgen in Thousand Oaks, CA, seeks an Associate Quality Assurance to ensure sampling and... ...performing quality reviews within a GMP environment. Training can be provided... ...needed. The candidate will contribute to continuous improvement projects, operate essential lab...Suggested
- Amgen in Thousand Oaks seeks a Sr. Associate Quality Assurance to support the Plant QA organization, providing daily oversight of Drug Product manufacturing and... .... Duties include electronic batch review, GMP document revision, maintenance work order approvals,...SuggestedShift work
- Takeda is seeking a Quality Assurance Validation Associate in Thousand Oaks to oversee validation deliverables and change controls, ensuring GMP and GxP compliance across facilities, utilities, equipment, and computerized systems. The role emphasizes risk assessment, traceability...Suggested
$104.29k - $141.09k
...organization the Drug Product QA Specialist provides... ...operational activities associated with the aseptic Drug... ...Safety and ensure we continue to meet Amgen standards... ...and drives continuous improvement projects in cross-functional... ...systems within GMP manufacturing environments...SuggestedFull timeFlexible hours- ...study stimuli for Human Factors activities. The ideal candidate has strong manual dexterity, experience with artwork production, labeling, and print workflows, and can work onsite at the client in a fast-paced, regulated environment. #J-18808-Ljbffr 3 Key Consulting, Inc.SuggestedContract work
$71.8k - $112.86k
...the role: As a Quality Assurance Validation Associate, you will work as part of cross-functional... ...include and implement all the applicable QA requirements. Participate in the risk... ...in all quality-related issues, including GMP regulations Assess and approve Change controls...Full timeLocal areaShift work- ...managing quality records, investigations, and cross-functional improvement initiatives. Responsibilities Partner with Manufacturing,... ...contamination control, environmental monitoring, and utility systems in GMP manufacturing Excellent written and verbal communication...
$100.45k - $135.9k
...collaboration, and approval of associated documentation.Generate and... ...microbiology teams to support process improvements, operational excellence... ...in a fast-paced, flexible GMP laboratory.Ability to generate... ...deadline for this position; we will continue accepting applications until...Full timeContract workWork experience placementFlexible hoursWeekend work- Amgen’s Thousand Oaks site seeks a Drug Product Quality Assurance Specialist to provide quality oversight for aseptic manufacturing and inspection areas. You will ensure compliance with cGMP, quality systems, and regulatory expectations while partnering with Manufacturing...Flexible hours
- ...customer requirements, internal procedures, and aerospace industry standards. The specialist plays a key role in supporting continuous improvement and maintaining regulatory compliance throughout the manufacturing process. Key Responsibilities: Prepare and submit...Work at office
- Job Description: FM Approvals is an international leader in third-party testing and certification services. We test property loss prevention products and services—for use in commercial and industrial facilities—to verify they meet rigorous loss prevention standards of...Work at officeWorldwideFlexible hoursNight shift
Do you want to receive more vacancies?
Subscribe and receive similar vacancies to Onsite QA Associate - GMP & Continuous Improvement. Be the first to apply!
Related searches
- qa technician Thousand Oaks, CA
- qa Thousand Oaks, CA
- quality assurance team leader Thousand Oaks, CA
- quality assurance Thousand Oaks, CA
- quality assurance representative Thousand Oaks, CA
- work from home qa testing Thousand Oaks, CA
- lead qa Thousand Oaks, CA
- continuous improvement Thousand Oaks, CA
- director continuous improvement Thousand Oaks, CA
- continuous improvement lead Thousand Oaks, CA



