Quality Assurance Specialist Jobs in Alberta
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.
Trials, etc., Advanced technical knowledge in global regulations and industry standards as they apply to clinical research, medical devices and pharmaceuticals and in the conduct of clinical study...
Quality Assurance Specialist Online Courses and Training Opportunities
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Salary for Quality Assurance Specialist Jobs in Alberta
Highest Education Level
Quality Assurance Specialists in Alberta 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
- Quality Systems
- Implementation
- Air Quality
- 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
- Clinical Data Management
- ICH Guidelines
- Drug Development
- Biology
- Pharmacovigilance
- Environmental Monitoring
- Stem Cells
- Microbiology
- Biotechnology
- Clinical Trials
- Clinical Research
- Genetics
- Medical Device Sales
- Data Science
- Good Manufacturing Practices
- FDA Regulations
- Corrective Actions & Preventive Actions
- Standard Operating Procedures
- Machine Learning
- Engineering
- Risk Management
- Military Background
- Auditing
- Investigation
- Collaboration
- Documentation
- Quality Assurance
- Reporting
- Bachelor's Degree
- Education Experience
- Regulations
- Policy Development
- Microsoft Office
- Problem Solving
- Sales
- Research Skills
- Microsoft Excel
- Organization
- Scheduling
- Leadership
- Communication Skills
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