{ “@context”: “http://schema.org”, “@type”: “JobPosting”, “title”: “Validation Engineer”, “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 parent QMS master plans.
- Validate manual assembly steps
Background
- Bachelor’s degree in Engineering (Manufacturing, Mechanical, , or Biomedical) or a related scientific discipline.
- 8+ years of direct experience in manufacturing validation and quality assurance within a highly regulated industry
- trong, working knowledge of regulatory guidelines and standards like FDA 21 CFR Part 11 & ISO13485
- Understanding of metrology, calibration tolerances, and NIST-traceable standards.
PLEASE NOTE THIS IS A CONTRACT ROLE
”, “datePosted”: “2026-05-21”, “hiringOrganization”: { “@type”: “Organization”, “name”: “Oxford Global Resources”, “sameAs”: “https://uk.whatjobs.com/pub_api__cpl__438878275__4861?utm_campaign=publisher&utm_medium=api&utm_source=4861” }, “jobLocation”: { “@type”: “Place”, “address”: { “@type”: “PostalAddress”, “addressLocality”: “” } } }Company: Oxford Global Resources
Location:
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 parent QMS master plans.
- Validate manual assembly steps
Background
- Bachelor’s degree in Engineering (Manufacturing, Mechanical, , or Biomedical) or a related scientific discipline.
- 8+ years of direct experience in manufacturing validation and quality assurance within a highly regulated industry
- trong, working knowledge of regulatory guidelines and standards like FDA 21 CFR Part 11 & ISO13485
- Understanding of metrology, calibration tolerances, and NIST-traceable standards.
PLEASE NOTE THIS IS A CONTRACT ROLE
…
Posted: May 21st, 2026