Quality Assurance Specialist Jobs in Westborough, MA
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.
Research Regulatory Compliance Specialist
- Brookline, MA (24 miles from Westborough, MA)
- 5 days ago
- Brookline, MA (24 miles from Westborough, MA)
- 5 days ago
Delivers education to study staff on various topics including good clinical practice, research regulations and the conduct of clinical trials....
Research Regulatory Compliance Specialist Boston Children's Hospital
- Brookline, MA (24 miles from Westborough, MA)
- 6 days ago
- Brookline, MA (24 miles from Westborough, MA)
- 6 days ago
Delivers education to study staff on various topics including good clinical practice, research regulations and the conduct of clinical trials....
Job Description: Compliance Specialist CMC Do you want to be part of an inclusive team that works to develop innovative therapies for patients? Every day, we are driven to develop and deliver...
Regional Compliance Manager Americas
- Waltham, MA (20 miles from Westborough, MA)
- 22 days ago
- Waltham, MA (20 miles from Westborough, MA)
- 22 days ago
Bring more to life. Are you ready to accelerate your potential and make a real difference within life sciences, diagnostics and biotechnology? At Leica Microsystems, one of Danahers 15+ operating...
QA Senior Compliance Specialist, Night Time Operations
- Framingham, MA (9 miles from Westborough, MA)
- 45+ days ago
- Framingham, MA (9 miles from Westborough, MA)
- 45+ days ago
Job Title: QA Senior Compliance Specialist, Night Time Operations Location: Framingham, MA About the Job We deliver 4.3 billion healthcare solutions to people every year, thanks to the flawless...
QA Principal Compliance Specialist, Operations
- Framingham, MA (9 miles from Westborough, MA)
- 90+ days ago
- Framingham, MA (9 miles from Westborough, MA)
- 90+ days ago
Job Title: QA Principal Compliance Specialist, Operations Location : Framingham, MA About the Job We deliver 4.3 billion healthcare solutions to people every year, thanks to the flawless planning...
Demographic Data for Westborough, MA
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Highest Education Level
Quality Assurance Specialists in Westborough, MA offer the following education backgroundQualifications / Skill Sets
The following top skills are often required or desired to land a Quality Assurance Specialist position
- Verbal Communication
- Filing
- Environmental Compliance
- NEPA
- CERCLA
- Environmental Management
- Quality Systems
- ISO Certified
- Implementation
- Air Quality
- Inspections
- ISO 13485
- Clean Water Act
- Environmental Education
- Clean Air Act
- Natural Resource Management
- ISO 14001
- Certified Hazardous Materials Manager
- Reimbursement
- GxP
- 21 CFR 820
- Institutional Review Board
- ICH GCP
- Clinical Data Management
- Good Clinical Practice
- Gene Therapy
- ICH Guidelines
- Field Sampling
- Biology
- Ecology
- Pharmacovigilance
- Good Laboratory Practice
- Biotechnology
- Clinical Trials
- Clinical Research
- Environmental Science
- Genetics
- FDA Regulations
- Medical Device Sales
- Corrective Actions & Preventive Actions
- Good Manufacturing Practices
- Standard Operating Procedures
- Engineering
- Affirmative Action
- Strategy Development
- Quality Control
- Investigation
- Written Communication
- Auditing
- Documentation
- Quality Assurance
- Collaboration
- Reporting
- Education Experience
- Bachelor's Degree
- Microsoft PowerPoint
- Regulations
- Policy Development
- Project Management
- Problem Solving
- Microsoft Office
- Microsoft Excel
- Time Management
- Staff Supervision
- Organization
- Research Skills
- Scheduling
- Leadership
- Communication Skills
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