Quality Assurance Specialist Jobs in Los Angeles, CA
A Quality Assurance (QA) Specialist in the biotechnology industry is responsible for ensuring that the biomedical products, pharmaceuticals, and medical devices produced meet strict quality standards. They conduct routine audits, develop quality control procedures, and oversee the manufacturing process to ensure compliance with legal regulations and industry standards. QA Specialists also assist in problem-solving efforts relating to quality management and perform regular inspections, documenting any discrepancies and implementing corrective actions when necessary.
A strong candidate for a QA Specialist typically requires a bachelor's degree in biology, chemistry, or a related field. They should have excellent attention to detail, strong communication skills, and the ability to work in a regulated environment. A working knowledge of FDA regulations, ISO standards, and GMP (Good Manufacturing Practices) is often required. Certified Quality Engineer (CQE), Certified Quality Auditor (CQA), or Certified Quality Improvement Associate (CQIA) are relevant certifications. Prior to becoming a QA Specialist, a person might have roles such as a Lab Technician, Quality Control Analyst, or Research Associate in the biotechnology field.
Staff International Regulatory Affairs Specialist
- Los Angeles, CA
- 6 days ago
- Los Angeles, CA
- 6 days ago
Summary As Staff Regulatory Affairs Specialist, you will be responsible for supporting MMS Dispensing products consisting of Medical Devices and Non-Medical Devices along with associated Software...
Research Compliance Manager California State University, Fullerton
- Fullerton, CA (21 miles from Los Angeles, CA)
- 8 days ago
- Fullerton, CA (21 miles from Los Angeles, CA)
- 8 days ago
Review Board (IRB)/human subjects protection administration....
Regulatory Affairs Specialist II
- Cypress, CA (16 miles from Los Angeles, CA)
- 18 days ago
- Cypress, CA (16 miles from Los Angeles, CA)
- 18 days ago
Regulatory Affairs Specialist II DiaSorin United States, California, Cypress 11331 Valley View Street (Show on map) Jun 14, 2025 Diasorin is a global leader in diagnostic solutions, pushing the...
Position: Contractual Compliance Analyst Location: Los Angeles, CA Compensation: $60,000-$75,000 Work Requirements: US Citizen, GC Holders or Authorized to Work in the US. The Contractual...
Research Compliance Analyst, Pathology & Laboratory Medicine
- Los Angeles, CA
- 90+ days ago
- Los Angeles, CA
- 90+ days ago
General Information Press space or enter keys to toggle section visibility Work Location : Los Angeles, USA Onsite or Remote Flexible Hybrid Work Schedule Monday - Friday, 8:00am - 5:00pm Posted...
Employee Relations and Compliance Manager
- Long Beach, CA (10 miles from Los Angeles, CA)
- 90+ days ago
- Long Beach, CA (10 miles from Los Angeles, CA)
- 90+ days ago
ABOUT ROCKET LAB Rocket Lab is a global leader in launch and space systems. The rockets and satellites we build and launch enable some of the most ambitious and vital space missions globally,...
General Information Press space or enter keys to toggle section visibility Work Location : Los Angeles, USA Onsite or Remote Flexible Hybrid Work Schedule Monday-Friday, 8:00am-5:00pm Posted Date...
Regulatory Affairs Specialist (CA)
- Torrance, CA (10 miles from Los Angeles, CA)
- 90+ days ago
- Torrance, CA (10 miles from Los Angeles, CA)
- 90+ days ago
Knowledge of cGMP Comfortable working directly for regulatory agencies, including the Food and Drug Administration (FDA), DEA, and Boards of Pharmacies Bachelor's degree in a relevant field (pharmacy, biology...
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Salary for Quality Assurance Specialist Jobs in Los Angeles, CA
Highest Education Level
Quality Assurance Specialists in Los Angeles, CA offer the following education backgroundQualifications / Skill Sets
The following top skills are often required or desired to land a Quality Assurance Specialist position
- English
- Driving
- Environmental Compliance
- Financial Services
- Quality Systems
- ISO Certified
- Geology
- Water Quality
- Implementation
- Air Quality
- Change Control
- Inspections
- ISO 13485
- Quality Management Systems
- Environmental Education
- Natural Resource Management
- Batch Record Review
- GxP
- TrackWise
- 21 CFR 820
- Institutional Review Board
- ICH GCP
- ICH Guidelines
- Lab Safety
- Biology
- Drug Development
- Biochemistry
- Pharmacovigilance
- Microbiology
- Environmental Monitoring
- Biotechnology
- Clinical Trials
- Clinical Research
- Laboratory Management
- Medical Device Sales
- FDA Regulations
- Corrective Actions & Preventive Actions
- Good Manufacturing Practices
- Standard Operating Procedures
- Product Development
- Engineering
- Risk Management
- Strategy Development
- Military Background
- Auditing
- Investigation
- Written Communication
- Interpersonal Skills
- Quality Assurance
- Collaboration
- Education Experience
- Documentation
- Reporting
- Bachelor's Degree
- Regulations
- Policy Development
- Microsoft Office
- Problem Solving
- Research Skills
- Microsoft Excel
- Organization
- Scheduling
- Leadership
- Communication Skills
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