Quality Assurance Specialist Jobs in Stillwater, MN
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 Integrity and Compliance Manager
- Minneapolis, MN (21 miles from Stillwater, MN)
- 13 days ago
- Minneapolis, MN (21 miles from Stillwater, MN)
- 13 days ago
About the Job The Research Integrity and Compliance (RIC) Manager is a managerial position of the Research Integrity and Compliance team responsible for managing the process to ensure that all...
Research Integrity and Compliance Manager University of Minnesota Twin Cities
- Minneapolis, MN (21 miles from Stillwater, MN)
- 15 days ago
- Minneapolis, MN (21 miles from Stillwater, MN)
- 15 days ago
The Research Integrity and Compliance (RIC) Manager is a managerial position of the Research Integrity and Compliance team responsible for managing the process to ensure that all research...
Diasorin is a global leader in diagnostic solutions, pushing the boundaries of science and technology to create cutting-edge tools that improve healthcare worldwide. With a legacy spanning over 50...
Sr Regulatory Affairs Specialist (Ad/Promo) (Remote) - Shockwave
- New Brighton, MN (16 miles from Stillwater, MN)
- 30+ days ago
- New Brighton, MN (16 miles from Stillwater, MN)
- 30+ days ago
Fueled by innovation at the intersection of biology and technology, we're developing the next generation of smarter, less invasive, more personalized treatments....
Remote WorkPrincipal Regulatory Affairs Specialist - Vascular (on-site)
- Saint Paul, MN (14 miles from Stillwater, MN)
- 30+ days ago
- Saint Paul, MN (14 miles from Stillwater, MN)
- 30+ days ago
Chemistry, life Sciences, Biology (or equivalent vocational qualifications) Experienced in regulatory submissions for Pharmaceutical, In vitro diagnostic devices and/or medical devices....
Global Respiratory Protection Regulatory Affairs Specialist
- Maplewood, MN (9 miles from Stillwater, MN)
- 45+ days ago
- Maplewood, MN (9 miles from Stillwater, MN)
- 45+ days ago
Your Skills and Expertise To set you up for success in this role from day one, 3M is looking for candidates who must have the following qualifications: Bachelors degree in Chemistry, Biology, Science...
Demographic Data for Stillwater, MN
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Salary for Quality Assurance Specialist Jobs in Stillwater, MN
Highest Education Level
Quality Assurance Specialists in Stillwater, MN 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
- 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
- Risk Management
- 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
- Staff Supervision
- Organization
- Research Skills
- Scheduling
- Leadership
- Communication Skills
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