Quality Assurance Specialist Jobs in Maplewood, 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.
Consulting Biologist - ESA Compliance Specialist
- Golden Valley, MN (15 miles from Maplewood, MN)
- 13 days ago
- Golden Valley, MN (15 miles from Maplewood, MN)
- 13 days ago
regular Consulting Biologist, depending on experience and skillset, and will be a motivated self-starter who possesses: Minimum of a bachelor's degree in Natural Resou ces, Wildlife Management, Wildlife Biology...
Senior Regulatory Affairs Specialist
- Stillwater, MN (9 miles from Maplewood, MN)
- 29 days ago
- Stillwater, MN (9 miles from Maplewood, MN)
- 29 days ago
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...
Senior Regulatory Affairs Specialist (on-site)
- Plymouth, MN (19 miles from Maplewood, MN)
- 60+ days ago
- Plymouth, MN (19 miles from Maplewood, MN)
- 60+ days ago
Provides mentoring and leadership to other Regulatory team members Required Qualifications Bachelor's Degree; preferably in a technical discipline such as biology, chemistry, microbiology, immunology...
Principal Regulatory Affairs Specialist - Vascular (on-site)
- Saint Paul, MN (5 miles from Maplewood, MN)
- 45+ days ago
- Saint Paul, MN (5 miles from Maplewood, MN)
- 45+ days ago
Chemistry, life Sciences, Biology (or equivalent vocational qualifications) Experienced in regulatory submissions for Pharmaceutical, In vitro diagnostic devices and/or medical devices....
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Global Respiratory Protection Regulatory Affairs Specialist
- Maplewood, MN
- 60+ days ago
- Maplewood, MN
- 60+ 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 Maplewood, MN
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Salary for Quality Assurance Specialist Jobs in Maplewood, MN
Highest Education Level
Quality Assurance Specialists in Maplewood, 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
- Environmental Compliance
- Waste Management
- Environmental Management
- Affirmative Action
- Quality Systems
- ISO Certified
- Implementation
- Air Quality
- Inspections
- ISO 13485
- Environmental Education
- ISO 14001
- Certified Hazardous Materials Manager
- GxP
- TrackWise
- 21 CFR 820
- Institutional Review Board
- ICH GCP
- Clinical Data Management
- Gene Therapy
- ICH Guidelines
- Good Clinical Practice
- Field Sampling
- Drug Development
- Biology
- Pharmacovigilance
- Stem Cells
- Good Laboratory Practice
- Clinical Trials
- Biotechnology
- Environmental Science
- Clinical Research
- Genetics
- Medical Device Sales
- FDA Regulations
- Corrective Actions & Preventive Actions
- Good Manufacturing Practices
- Standard Operating Procedures
- Engineering
- Strategy Development
- Risk Management
- Investigation
- Written Communication
- Auditing
- Documentation
- Quality Assurance
- Collaboration
- Bachelor's Degree
- Reporting
- Education Experience
- Microsoft PowerPoint
- Regulations
- Policy Development
- Project Management
- Problem Solving
- Research Skills
- Microsoft Office
- Microsoft Excel
- Time Management
- Staff Supervision
- Organization
- Scheduling
- Leadership
- Communication Skills
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