Senior GMP QA Associate - Floor & Documentation
BioSpace
BioSpace is seeking a Senior Associate Quality Assurance in Thousand Oaks, California, to oversee drug product manufacturing areas while ensuring regulatory compliance and supporting Amgen's Quality Assurance program. This role involves daily oversight and various quality control responsibilities to maintain product integrity. The ideal candidate will bring GMP experience and a strong understanding of aseptic principles alongside excellent organizational skills. You can expect a comprehensive benefits package including medical coverage and generous retirement contributions. #J-18808-Ljbffr BioSpace
- US Tech Solutions is seeking a Senior Associate, Quality Assurance to provide onsite QA support at their Thousand Oaks location. The role involves rotating between... ...will have QA or manufacturing experience in a GMP environment, strong critical thinking skills, and a...FloorSeniorRotating shiftDay shiftAfternoon shift
- Job Title: AutomationEngineer Senior, DeltaV/Rockwell PLCs/GMP - (JP15196) Location: Thousand Oaks, CA.... ...design, engineering and validation documentation and project execution. The ideal individual... ...• Purposeful Presence on the Floor (PPoF) Provide Continuous Improvement...FloorSeniorContract workWork experience placementWork at officeMonday to FridayShift work
- Amgen SA in Thousand Oaks, California, seeks a Senior Associate Quality Assurance professional to provide oversight for Drug Product manufacturing... ...electronic batch records and ensuring compliance with GMP standards. The ideal candidate will possess a strong background...FloorShift work
- Job Title: Software Engineer, Senior - Biopharma, GMP Lab Instruments Automation (JP13852) Location:... ...office based, lab based, manufacturing floor. Candidate will be lab and office... ...5 years of engineering experience or Associate degree and 10 years of engineering experience...FloorSeniorContract workWork experience placementWork at officeLocal areaWork from homeRelocationFlexible hours
- ...Description The manager is seeking a Senior Associate, Quality Assurance to provide real-time, floor-based QA support at USTO site. This... ...experience in a GMP environment (preferably within... ...maintaining training, and good documentation practices. Also, ability to make...FloorSeniorFlexible hoursShift workRotating shiftDay shiftAfternoon shift
- Job Title: MCS Manufacturing Senior Associate, Biopharma (JP10845) Location: Thousand Oaks, CA... ...performing all work while following GMP documents (SOPs) with strict adherence to safety... ...process - perform troubleshooting on the floor, initiate investigation and bring...FloorSeniorContract workShift workWeekend work
- Senior Associate Quality Assurance The Sr. Associate Quality Assurance... ...program under the Plant QA organization, providing... ...on the manufacturing floor (Form/Fill Grade 8... ...routine interventions and documentation. Electronic batch record review GMP Document (SOPs/FORMs) revision...FloorSeniorFlexible hoursShift workAfternoon shift
- Senior Associate Quality Assurance This role supports Amgen’s... ...program under the Plant QA organization,... ...compliance, reviewing documentation, and supporting quality... ...on the manufacturing floor (Form/Fill Grade 8 Gowning... ...Electronic batch review GMP document (SOPs/FORMs)...FloorSeniorFlexible hoursShift work
- Senior Associate Manufacturing Per the Manufacturing Senior Associate role... ..., reviewing and audit documentation, applying knowledge of MES,... ...processing operations on the mfg. floor Identify and propose solutions... ...writing capability GMP knowledge with ability to interpret...FloorSeniorFlexible hours
- Inc. (Vti) is seeking a Senior Validation Lead in Thousand Oaks, California. The role requires... ...in leading validation activities for GMP qualification across various systems and... ...teams and managing validation documentation. Hands-on experience with relevant tools...Senior
- ...requires a Bachelor's degree in Life Sciences and at least 1 year of related experience in quality assurance or manufacturing within the GMP pharmaceutical or medical device industry. Responsibilities include evaluating product complaint samples, managing inventory, and...Senior
- Amgen in Thousand Oaks, California seeks a Senior Associate Quality Control - Microbiology to support the... ...microbial assessments and testing. You will perform documentation, troubleshooting, and equipment operation in a fast-paced GMP laboratory. The ideal candidate will have...SeniorFlexible hours
- Senior Associate Manufacturing What you will do Let’s do this. Let’s change the world. In this... ...performing all work while following GMP documents (SOPs) with strict adherence to safety... ...process - perform troubleshooting on the floor, initiate investigation and bring...FloorSeniorFlexible hoursShift workWeekend work
- Amgen SA is looking for a Senior Associate in Quality Control - Microbiology to support the QC Microbiology and Environmental... ...microbial testing, managing sample and data documentation, and ensuring compliance with safety and GMP guidelines. The ideal candidate will have a...Senior
- SSi People is looking for an MCS Senior Associate Quality Assurance in Thousand Oaks, California. This role requires delivering real-time quality... ...flexibility in shift rotations, and hands-on experience in a GMP environment. The ideal candidate will have strong attention to...SeniorShift work
- ...best of my knowledge. About the role The Senior Project Management Lead is a critical... ...schedules, risk mitigation, communications, and documentation. Support project prioritization and... ...Requirements Mix of office work and on-floor presence within the facility. Occasional...FloorSeniorFull timeWork at officeLocal areaFlexible hoursWeekend work
- A leading consulting firm is seeking an MCS Manufacturing Senior Associate to join their client's dynamic biopharmaceutical team in Thousand... ...activities, leading projects, and providing expertise within a GMP environment. Candidates should possess a degree in Engineering...Senior
- ...you will work with various teams to develop project scope and manage implementation. Responsibilities include ensuring compliance with GMP, leading project strategies, and developing accurate cost estimates. The ideal candidate should have a bachelor's degree in...SeniorWork experience placement
- ...and periodic review programs for various clients in regulated industries. This role plays a critical part in ensuring compliance with GMP and quality standards. The ideal candidate will possess a Bachelor's degree and have extensive experience in pharmaceutical and...Senior
- Job Title Senior Automation Engineer - DeltaV DCS / Rockwell PLC & SCADA (GMP Biopharma Capital Projects) Job ID JP15356 Location... ...the SOPs, and training documents, delivering spare parts list,... ...degree and 7 years of experience Associates degree and 12 years of experience...SeniorPermanent employmentContract work
- ...product manufacturing operations at our Thousand Oaks facility. This role requires managing operational schedules ensuring compliance with GMP and supporting new product introductions. The ideal candidate will possess a strong background in drug product manufacturing, with...SeniorFlexible hours
- BioSpace is seeking a Senior Associate for Quality Control in Microbiology in Thousand Oaks, California. This role involves supporting... ...and Environmental Monitoring team with microbial testing and documentation. Ideal candidates will possess a Bachelor’s degree or...SeniorFlexible hours
- ...Bachelor's Degree in Life Sciences or a related field, with at least 1 year of experience in quality assurance or manufacturing in a GMP environment. Strong attention to detail, project management skills, and proficiency in word processing and spreadsheet tools are essential...Senior
$22 - $32 per hour
...experience. Typically 1 plus years of related quality assurance or manufacturing experience in a GMP pharmaceutical or medical device industry. Tasks and Expectations Evaluate documentation and operation according to company guidelines. Be self‑motivated, attentive to details,...SeniorSummer work- ...with a 30min lunch. Local Candidates only. No relocations. Lab Based Job. Education Bachelor's degree. Nice to have: documentation practices, GMP, previous lab experience. Hiring Manager Notes What type of qualities/characteristics are you looking for in...SeniorWork experience placementSummer workLocal areaRelocationFlexible hoursShift work
$27 - $29 per hour
...shipment inventory for delivery to patients via the Mail Center. Document receipt of incoming packages from complainants and open packages... ...of related quality assurance or manufacturing experience in a GMP pharmaceutical or medical device industry. Top 3 Must Have Skill...SeniorHourly payFull timeLocal areaFlexible hours- ...company in Thousand Oaks, California is seeking a Quality Operations Specialist. The role encompasses ensuring GMP compliance, supporting batch documentation review, and collaborating with cross-functional teams. Ideal candidates will have a Bachelor's degree in Life Sciences...Full time
- ...Principal (DeltaV/PLC/Scada), Biopharma/GMP - (JP13780) Location: Thousand Oaks, CA.... .../hour W2 DOE with benefits, open to less Senior as well. Posting Date: 2/27/2025 Target start... ...team, revising the SOPs, and training documents, delivering spare parts list, updating Maximo...Long term contractContract work
- Amgen is seeking a Drug Substance Quality Assurance Specialist in Thousand Oaks to provide vital quality oversight for manufacturing operations. The role demands adherence to cGMP, ensuring compliance and safety in manufacturing processes. The specialist will engage with...
- ...organization, the Drug Substance QA Specialist provides quality... ...quality and compliance oversight of GMP processes, procedures,... ...thoroughly investigated, appropriately documented, and resolved in accordance... ...4 years of quality experience Associate’s degree and 8 years of...Flexible hours
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