Quality Assurance Specialist Jobs in Florida
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.
Job Title: RCRA Specialist / Sr. Waste Coordinator Job Description We are seeking a dedicated RCRA Specialist to support operational efforts in ensuring compliance with local, state, and federal...
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Requirements Required Qualifications: Bachelor's degree in Life Sciences, Biology, Biotechnology, or a related field preferred....
Regulatory Affairs Specialist (On-site)
- Palm Beach Gardens, FL
- 16 days ago
- Palm Beach Gardens, FL
- 16 days ago
We are ZimVie, a publicly traded, global life sciences leader focused on restoring daily life by advancing clinical technology to improve patients' smiles, function, and confidence. Our company is...
Sr Product Stewardship & Regulatory Affairs Specialist Job
- Mulberry, FL
- 23 days ago
- Mulberry, FL
- 23 days ago
Degree in relevant field of study (e.g. environmental science, biology, chemical engineering, chemistry, toxicology) or equivalent Minimum of 5 years experience in product stewardship/regulatory affairs...
RWD Compliance Manager Company: Norstella Location: Remote, United States Date Posted: May 23, 2025 Employment Type: Full Time Job ID: R-1204 **Description** **About Norstella:** At Norstella, our...
Senior Corporate Compliance Manager - Training, Communications & Policy (Remote)
- Tallahassee, FL
- 29 days ago
- Tallahassee, FL
- 29 days ago
California, US residents click here (. **The job details are as follows:** Who we are We are the first publicly-traded biotech or pharmaceutical company to take the form of a public benefit...
Quality Assurance Associate (Pompano Beach, FL)
- Pompano Beach, FL
- 30+ days ago
- Pompano Beach, FL
- 30+ days ago
Client is seeking an entry-level Quality Assurance / Quality Control Associate to support clinical manufacturing and drug development activities in a GMP-regulated environment. This is a great...
Career Category Information Systems Job Description Join Amgens Mission of Serving Patients At Amgen, if you feel like youre part of something bigger, its because you are. Our shared missionto...
Accelerate your career. Join the organization that's driving the world's technology and shape the future. Ingram Micro is a leading technology company for the global information technology...
Location:Lee Health Corporate Center -4211 Metro ParkwayFort Myers FL 33916 Department: Compliance Work Type: Full Time Shift: Shift 1/8:00:00 AM to 4:00:00 AM Minimum to Midpoint Pay Rate:$38.48...
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Salary for Quality Assurance Specialist Jobs in Florida
Highest Education Level
Quality Assurance Specialists in Florida 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
- Analytical Skills
- Environmental Compliance
- Quality Systems
- ISO Certified
- Flexibility
- Implementation
- Air Quality
- Document Control
- Change Control
- Inspections
- ISO 13485
- Quality Management Systems
- Environmental Education
- Batch Record Review
- Internal Audits
- GxP
- TrackWise
- 21 CFR 820
- Institutional Review Board
- ICH GCP
- Cancer Research
- ICH Guidelines
- Good Clinical Practice
- Drug Development
- Biology
- Environmental Monitoring
- Stem Cells
- Microbiology
- Biotechnology
- Clinical Trials
- Clinical Research
- Medical Device Sales
- Data Science
- Good Manufacturing Practices
- FDA Regulations
- Corrective Actions & Preventive Actions
- Standard Operating Procedures
- Engineering
- Strategy Development
- Risk Management
- Military Background
- Investigation
- Auditing
- Written Communication
- Collaboration
- Documentation
- Quality Assurance
- Reporting
- Bachelor's Degree
- Education Experience
- Regulations
- Policy Development
- Microsoft Office
- Problem Solving
- Sales
- Research Skills
- Microsoft Excel
- Teamwork
- Organization
- Scheduling
- Leadership
- Communication Skills
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