KH
Validation Specialist
Katalyst Healthcares & Life Sciences
π¨π¦ Canada | πΊπΈ United States
On-site
Manager or above
1 week ago
- Change Management
- GMP
- MS Office
- Excel
- Technical Writing
1 week ago
- We are seeking a hands-on Equipment Qualification & Process Validation Contractor to support the Enterprise Quality β Change Management & Systems organization.
- The contractor will be responsible for executing qualification activities, including Installation Qualification (IQ), Operational Qualification (OQ), and Performance Qualification (PQ), for manufacturing equipment, processes, and materials within a regulated manufacturing environment.
- This is an execution-focused role, with day-to-day direction from the Manager.
- Success will be measured by the timely, accurate, and right-first-time completion of qualification deliverables.
Responsibilities:
- Execute and close IQ/OQ/PQ protocols for manufacturing equipment and systems.
- Author protocols, qualification reports, and GMP-compliant documentation.
- Document deviations/discrepancies and maintain full record traceability.
- Coordinate qualification activities with Manufacturing, Engineering, Quality, and Project teams.
- Support change control, documentation remediation, and record management.
- Execute qualification activities on the factory floor around production schedules.
Qualifications:
- Bachelor's degree in a technical discipline or equivalent experience.
- 5+ years of hands-on IQ/OQ/PQ and process validation experience in GMP or regulated manufacturing.
- Experience with protocol writing, execution, reports, deviations, and traceability.
- Proficiency with eQMS (TrackWise or similar), document management systems, and MS Office/Excel.
- CQE, CQA, ASQ, or similar certification preferred.
Top 3 Skills:
- IQ/OQ/PQ & Process Validation.
- Technical Writing & GMP Documentation.
- Cross-Functional Coordination & Factory-Floor Execution.
Validation Specialist Β· Katalyst Healthcares & Life Sciences