Director of Quality Assurance and Regulatory Affairs Remote & Hybrid Only Jobs in Massachusetts
Senior Manager, Quality Assurance Investigations in Devens, MA
- Bristol Myers Squibb
- Devens, MA
- 8 hours ago
- Devens, MA
- 8 hours ago
Each of us is empowered to apply our individual talents and unique perspectives in a supportive culture, promoting global participation in clinical trials, while our shared values of passion, innovation...
HybridSenior Manager, Quality Assurance - Lab Operations
- Bristol Myers Squibb
- Devens, MA
- 16 days ago
- Devens, MA
- 16 days ago
In-depth knowledge of cGMP, GLP, ICH guidelines, and data integrity principles....
HybridSenior Manager, Regulatory Affairs
- rapport Therapeutics
- Boston, MA
- 19 days ago
- Boston, MA
- 19 days ago
Our first indication targets focal epilepsy with additional clinical trials for neuropathic pain and bipolar disorder....
HybridJob Title: Director, Regulatory Affairs Location: [Boston, MA or Hybrid/Remote] Industry: Biotechnology / Biopharma Type: Full-time About the Opportunity Im working with an innovative biotech...
HybridDirector, Regulatory Affairs - Clinical Strategy
- Azurity Pharmaceuticals
- Woburn, MA
- 45+ days ago
- Woburn, MA
- 45+ days ago
trials including but not limited to efficacy, safety, pharmacovigilance, and clinical pharmacokinetics Participate/lead FDA and Health Authority interactions regarding clinical regulatory aspects,...
HybridDemographic Data for Massachusetts
Moving to Massachusetts? Find some basic demographic data about Massachusetts below.
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Highest Education Level
Director of Quality Assurance and Regulatory Affairss in Massachusetts offer the following education backgroundQualifications / Skill Sets
The following top skills are often required or desired to land a Director of Quality Assurance and Regulatory Affairs position
- Study Management
- DNA/RNA Extraction
- Molecular Cloning
- Immunofluorescence
- Gene Therapy
- Next Generation Sequencing
- Virology
- Transfection
- Pharmacovigilance
- Internal Audits
- Medical Affairs
- Batch Record Review
- Lab Safety
- ICH Guidelines
- Drug Development
- Clinical Laboratory Operations
- Experimental Design
- ISO 13485
- GxP
- Good Clinical Practice
- Quality Systems
- Good Laboratory Practice
- Enzyme-Linked ImmunoSorbent Assay
- Microscopy
- Cell Culture
- Molecular Biology
- Biotechnology
- Biology
- Quality Management Systems
- Polymerase Chain Reaction
- Laboratory Management
- Microbiology
- Validation
- Clinical Trials
- Good Manufacturing Practices
- FDA Regulations
- Standard Operating Procedures
- Product Development
- Continuous Improvement
- Strategy Development
- Engineering
- Quality Control
- Implementation
- Auditing
- Documentation
- Collaboration
- Interpersonal Skills
- Investigation
- Reporting
- Inventory Management
- Mentoring
- Quality Assurance
- Bachelor's Degree
- Policy Development
- Education Experience
- Project Management
- Research Skills
- Regulations
- Microsoft Office
- Staff Supervision
- Microsoft Excel
- Problem Solving
- Scheduling
- Leadership
- Communication Skills
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