Quality Assurance Specialist
1 week ago
JOB SUMMARY
Document management for medical device records and forms, both customer supplied and internal.
NATURE AND SCOPE
Duties and Responsibilities:
Internal Quality Audits
Process documentation and auditing
In-process and final inspection of medical devices
Testing of product
Other duties as required
Skills and Abilities:
Excellent organizational skills
Communication skills written and verbal
Process documentation experience
Advanced computer skills (MS Office)
EMPLOYMENT REQUIREMENTS
Educational Requirements:
Post secondary education
Years of Experience:
5 + years experience in Quality Assurance.
Specialization Required:
Knowledge and experience with FDA Quality System Regulations for medical devices
Knowledge and experience with GMP
F046 Rev 2
**Job Types**: Full-time, Permanent
**Benefits**:
- Company events
- Dental care
- Extended health care
- Life insurance
- On-site parking
- Paid time off
- Vision care
Schedule:
- 8 hour shift
- Day shift
- Monday to Friday
- Overtime
Supplemental pay types:
- Overtime pay
Ability to commute/relocate:
- Stittsville, ON: reliably commute or plan to relocate before starting work (required)
**Experience**:
- quality assurance: 1 year (preferred)
Work Location: One location
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