GMP Validation Engineer | Quality & Compliance

Oxoid Remel Microbiology

Basingstoke

On-site

GBP 50,000 - 65,000

Full time

4 days ago
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Benefits offered by this job

Competitive salary
Annual merit-based pay increases
Medical benefits
Paid annual leave
Employee referral bonus
Career development and advancement

Job summary

Oxoid Remel Microbiology in the United Kingdom is seeking a Validation Engineer to help keep manufacturing processes, equipment, and systems validated and compliant. The role emphasizes quality, regulatory compliance, and reliability while collaborating with cross-functional teams in a GMP environment.

The engineer will plan, execute, and maintain validation docs, support qualification activities, perform risk and impact assessments, and assist audits and inspections to continuously improve the

Qualifications

  • Experience in GMP/regulatory environments is essential.
  • Ability to create clear, compliant validation documentation.
  • Experience with risk-based approaches and lifecycle management.

Responsibilities

  • Plan, prepare, execute, and maintain validation documentation.
  • Support equipment, utilities, facilities, and processes qualification.
  • Collaborate with Manufacturing, Engineering, Quality, and Regulatory Affairs.
  • Perform risk assessments and investigations supporting changes and deviations.
  • Review validation records and ensure compliance with GMP and site procedures.
  • Assist audits and inspections and support validation program improvements.

Skills

GMP knowledge
Documentation skills
Cross-functional teamwork
Analytical thinking
Technical writing

Education

BSc in Engineering or Life Sciences

Job description

Oxoid Remel Microbiology in the United Kingdom is seeking a Validation Engineer to help keep manufacturing processes, equipment, and systems validated and compliant. The role emphasizes quality, regulatory compliance, and reliability while collaborating with cross-functional teams in a GMP environment.

The engineer will plan, execute, and maintain validation docs, support qualification activities, perform risk and impact assessments, and assist audits and inspections to continuously improve the

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