Biotech QA Specialist: QC & Compliance
Bionova Scientific
Bionova Scientific LLC is seeking a QA Specialist in Fremont, CA to provide Quality Assurance for QC and Analytical Laboratories in a fast-paced CDMO. You will handle investigations, self-inspections, data reviews, and change control in GMP environments. Qualifications include a Bachelor’s in sciences, 2–4 years GMP-related experience, and strong documentation/communication skills. The role supports cGMP audits and document control tasks within a collaborative team. #J-18808-Ljbffr Bionova Scientific
- ...Scientific LLC in Fremont, CA is seeking a QA Specialist (Full Time) to provide QA for QC and Analytical Laboratories in a fast-paced biotech CDMO. The role focuses on investigations... ..., change control, SOPs, and ensure cGMP compliance, with collaboration across Manufacturing...SuggestedFull time
$36 - $48 per hour
...Scientific LLC Job Description: The QA Specialist will provide Quality Assurance for... ...job, with a focus on QA expectations for QC activities. The position requires diverse... ...materials in QAD ERP System. Evaluate compliance of completed manufacturing records (...SuggestedFull timeTemporary workWork at office$36 - $48 per hour
...QA SpecialistThe QA Specialist will provide Quality Assurance for Quality Control and Analytical Laboratories... ...with a focus on QA expectations for QC activities. The position requires... ...materials in QAD ERP System.Evaluate compliance of completed manufacturing records (sample...SuggestedFull timeTemporary workWork at office$95k - $110k
...Quality Assurance Compliance Team MemberBionova Scientific LLC is seeking a Quality Assurance Compliance Team Member. This role is part of the Quality Assurance Compliance team. As a member of the QA team, the role incumbent has GMP Quality experience assessing supplier...SuggestedWork at office$95k - $110k
Bionova Scientific, Inc. is seeking a Quality Assurance Specialist in Fremont, CA to ensure supplier compliance and maintain quality standards. The role involves assessing suppliers, managing quality agreements, and conducting audits. Candidates should have at least 5 years...SuggestedFull time- Protagonist Therapeutics is seeking a Specialist/Sr. Specialist, Quality Assurance to perform GMP QA activities supporting manufacturing. The role reports to the... ...per week. The position requires 5+ to 8+ years in biotech/pharma QA and willingness to travel up to 25% (...Work at office
- ...to define and drive global quality and regulatory programs across QA, QC, validation, and supplier quality. This executive role partners with cross-functional leaders to ensure cGMP, GLP, GCP compliance and successful regulatory submissions. The successful candidate will...
$20k
...Review Risk Assessments, Process Development Reports, and Protocols. Quality support of the validation system to ensure quality and compliance requirements are met in an efficient and effective manner. Quality support and approval of validation related documentation (e.g....Contract workWorldwide2 days per week$21.88 - $32.84 per hour
...Code: 94587 Travel Percentage: 0 Compensation Range: $21.88 - $32.84 The compensation range provided is in compliance with state specific laws. Factors that may be used to determine your actual rate of pay include your specific skills, years of experience...Work at officeLocal areaWorldwideNight shift- Delta Electronics Americas is seeking a Risk & Quality Management professional in Fremont, CA. The role provides independent risk assessment and quality oversight across High-Value and At-Risk SI projects throughout the lifecycle, ensuring adherence to Delta’s standards...
$105k - $125k
Job Summary:The Sr. Specialist, Quality Assurance is an intermediate level position with hands-on QA experience. Under moderate supervision, the individual will be working... ...of quality assurance activities to ensure compliance with Revance procedures, applicable US and international...Work at officeLocal areaFlexible hours$105k - $129k
...Quality Assurance Specialist III, AnalyticalArdelyx is a commercial-stage biopharmaceutical company focused on redefining treatment approaches... ...(OOT), and other atypical analytical results, while ensuring compliance with applicable GMP regulations and internal procedures. The...Full timeContract workWork at officeFlexible hours2 days per week3 days per week- Quality Assurance Associate Start your career in quality control with ultimate flexibility! We have immediate openings for quality assurance associates to support production on short-term mandates. This role is perfect for detail-oriented individuals who are comfortable...Temporary workImmediate startRemote workShift work
- ..., supporting documentation) for accuracy, completeness, and GMP compliance. Review analytical methods, method validation protocols/reports,... ...related field + 5+ years in analytical development, manufacturing, or QA in biotechnology (or equivalent). 3+ years experience in a GMP...Contract workFlexible hours
- Scorpion Therapeutics is seeking an experienced QA professional to review analytical quality documentation supporting regulatory submissions and batch dispositions. The role emphasizes GMP compliance, method validation oversight, and collaboration with CMOs and laboratories...
$25 per hour
...accepted components from rejected materials, ensuring the accurate segregation of non-conforming items. - Accurately fill out simple qc logs and inspection checklists to record findings hourly or batch-by-batch. - Collect samples of materials or components at...Hourly payTemporary workWork experience placementLocal areaImmediate startShift work$24 - $33 per hour
...Job Title:Quality Specialist Hourly:$24 - $33 Location:Fremont, CA (On-site) Type:Full-... ...01 Quality Management System (QMS). The QA Auditor coordinates closely with Production... ...Corporate QA teams to monitor real-time compliance, identify process drift, and enforce...Hourly payFull timeLocal areaImmediate start- ...document control, and validation programs. The candidate will review and author validation documents, assess risk, and collaborate with Operations, Manufacturing, QC and Validation to maintain GXP asset integrity and continuous process improvement. #J-18808-Ljbffr CSBio Co.
- ...role based in Fremont, CA or Salt Lake City, UT.As the Senior Staff Clinical Quality Associate, you will focus on clinical quality, compliance governance, and regulatory readiness across global clinical research activities. You will provide oversight of quality systems,...Full timeFor contractors
$75k - $80k
...Quality Assurance Specialist /AuditorLeanTeq is best-in-class in a very niche part of the semiconductor industry and is looking for quality... ...for managerial reviewCompliance SupportMonitor and update compliance software.Other compliance projects as required.Other duties as...Work at officeNight shift$23 per hour
...you to apply your precision inspection skills when it fits your life. Your responsibilities: - Perform routine quality control (qc) inspections on components, sub-assemblies, or finished products based on detailed standard operating procedures (sops) and visual aids...Temporary workWork experience placementLocal areaImmediate startFlexible hours- Overview Of Position LeanTeq is best‑in‑class in a very niche part of the semiconductor industry and is looking for quality‑oriented people who enjoy working in a great culture to join our team. Our company does chemical cleaning of the manufacturing parts for the semi‑...
- LeanTeq 濂達科技 in Milpitas, California, is seeking a dedicated Quality Assurance Specialist. The role focuses on ensuring compliance with quality standards like ISO 9001:2015 and ISO/IEC 17025:2017, driving process improvements, and conducting audits. Ideal candidates will...
- ...Quality System Specialist Unigen, headquartered in Newark, California, is a trusted partner for businesses seeking to power their next... ...001), and Information Security (ISO 27001). This role ensures compliance with applicable standards, legal requirements, and customer...
- PPG Quality busca Auditores para garantizar la precisión de los envíos salientes y mantener altos estándares de calidad en el control de calidad. El rol es ideal para profesionales con experiencia de vida que deseen permanecer activos y contribuir en logística. Las responsabilidades...
- ...for Visa Sponsorship. Position Overview As a Senior Quality Specialist at Nestlé Nutrition & Health, your mission is to ensure quality... ...and food safety in their own job deliverables. Ensures full compliance to Nestlé Standards and Regulatory requirements. Provides support...
- Aperia Technologies is hiring a Quality Assurance Technician to conduct product testing, analyze results, and perform failure analysis to ensure our Halo technologies meet quality standards. You will log data, support ORT and RMA processes, maintain the FA lab, and uphold...
- Quanta Manufacturing Fremont is seeking a Quality Specialist to execute end-to-end Patrol Audit systems and accountability programs... ...with Production Operations, Training, and Corporate QA to monitor compliance and drive improvements. #J-18808-Ljbffr Quanta Manufacturing...
- Pentagon Technologies, Inc. is seeking a Quality Technician for the second shift in Hayward, CA. This role focuses on executing quality controls, audits, and risk management for materials, equipment, and processes under direct supervision. The ideal candidate will have ...Afternoon shift
$25.61 per hour
...shipment tracking activities. Quality Control & Inspection Inspect incoming materials, components, and finished goods to ensure compliance with company quality standards and specifications. Perform visual inspections and basic dimensional inspections using...H1bLocal areaImmediate startTrial periodShift work
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