Job Description
Our Client are in Belfast is expanding and the Program manager for the Manufacturing Quality group tasked with integration of the QMS is looking for a Senior Manufacturing Validation consultant,
Manufacturing Validation Consultant.
Full time onsite (occasional hybrid)
LOA – 18 months -2 years
Start – end of June
- Plan and execute the re-qualification of existing manufacturing equipment (IQ, OQ, PQ) to meet corporate and regulatory standards.
- Assess and update Process Validation Master Plans (PVMP) to reflect updated
- Align local manufacturing Standard Operating Procedures (SOPs) with the newly adopted QMS requirements. (1 )
- Perform rigorous risk assessments (e.g., FMEA) on transitioning production lines to mitigate risks during the system switchover.
- Harmonise legacy equipment calibration schedules with paren...
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Submit ApplicationJob Details
- Location belfast metropolitan area, belfast metropolitan area
- Job Type Full-time
- Category Medical Equipment Manufacturing
- Posted Date June 06, 2026
- Application Deadline July 16, 2026