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About the Role
The Advanced QC Technician will support the Consumables Manufacturing team on the swing shift to meet company goals related to safety, quality, continuous improvement, and daily production targets for cartridges.
Responsibilities
- Perform detailed inspections of materials, components, and finished products to ensure compliance with specifications, tolerances, and standards.
- Conduct assay testing using laboratory equipment to validate the performance of consumable cartridges.
- Maintain accuracy in test records, travelers, logs, and quality documentation.
- Accurately document findings, anomalies, and deviations, compiling data for product quality reports, CAPAs, and risk assessments.
- Assist in revising or developing standard operating procedures (SOPs) and work instructions.
- Support audits by preparing and presenting quality documentation for regulatory inspections or internal reviews.
- Identify trends in quality control data to highlight recurring issues and propose process improvements.
- Collaborate with engineering, manufacturing, and R&D teams to implement corrective and preventive actions (CAPAs) and process enhancements.
- Train and mentor junior technicians on quality standards and inspection/assay testing techniques.
- Ensure all work complies with quality management systems, following Good Manufacturing Practices (GMP).
Requirements
- Minimum of 2 years of quality control experience in the medical device, pharmaceutical, or life sciences industry.
- Proficiency in using lab equipment, inspection tools, software, and testing methodologies.
- Familiarity with statistical analysis and tools like JMP is a plus.
- Strong analytical skills to diagnose and resolve quality issues effectively.
- Excellent written and verbal communication skills for preparing technical documentation and liaising with multidisciplinary teams.
- Detail-oriented and committed to quality excellence.
- Strong time management skills with the ability to handle multiple responsibilities and meet deadlines.
- Team player who thrives in cross-functional environments and fosters collaboration.
- Passion for innovation and continuous learning in the life sciences and medical technology field.
Skills
- Quality Inspection
- Assay Testing
- Laboratory Equipment Operation
- Documentation
- Reporting
- CAPA Management
- SOP Development
- Process Improvement
- Statistical Analysis
- Communication
Location
- Onsite
Work Type
- Full-time
- Swing Shift
Experience Level
- 2+ years
Education Level
- BS in Biology, Chemistry, Biochemistry or related discipline preferred
Salary/Compensations
- $20.00 - $27.50 per hour
- Eligible for target annual cash bonus
Benefits
- Medical insurance
- Dental insurance
- Long-term disability insurance
- Life insurance
- Group income protection
- Personal accident insurance
- Travel insurance
- Group Registered Retirement Savings Plan (Group RRSP)
- Tax-Free Savings Account (TFSA) option
- Mentorship
- Promotional opportunities
- Training and development
- Tuition reimbursement
- Internship programs
- Employee resource groups
- Paid time off for volunteering
- Employee events
- Charity drives
- Accrued leave policy
- Paid holidays
- Paid time off
- Paid parental leave
About the Company
- Bio-Techne enables cutting-edge research in Life Sciences and Clinical Diagnostics.
- Bio-Techne and its brands provide tools for researchers to further treat and prevent disease worldwide.
- Fosters a culture of empowerment and innovation, where employees feel valued and encouraged to bring new ideas to the table.
Equal Opportunity
- All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, or status as a protected veteran.
- Bio-Techne will not accept unsolicited resumes from any source other than a candidate application.
- Requests for reasonable accommodation during the application process can be made by contacting hr@bio-techne.com.