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Contamination Control Manager

United Kingdom, Falkirk · Job Posted May 13, 2026
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Job Description

At SRG, we are excited to be partnering with our client, a biologics Contract Development and Manufacturing Organisation (CDMO), to appoint an experienced Contamination Control Manager. This is a senior, high-impact role for a contamination control leader who combines deep technical expertise with strong on-the-floor influence, embedding contamination control into systems, behaviours, and decision-making across a multi-facility, multi-client manufacturing environment.

Job Responsibility

  • Own and evolve the site Contamination Control Strategy in line with EU/UK GMP Annex 1, FDA and ICH expectations
  • Embed contamination control principles into facility and equipment design, process flows, cleaning and sterilisation strategies, supplier management and training programmes
  • Partner with Manufacturing to influence aseptic behaviours, shift routines, operator decision-making and capability development
  • Collaborate with MSAT across equipment design, tech transfer, scale-up, process characterisation and new product introduction
  • Ensure full integration of the CCS with Quality systems including deviations, investigations, CAPAs, change control and audit readiness
  • Lead contamination-focused risk assessments (including FMEA) across client processes, shared equipment, utilities, campaign manufacturing and changeovers
  • Translate risk into practical, executable operational controls and maintain assessments as living tools informed by data and trends
  • Design and deploy contamination control training tailored to a CDMO environment, reinforcing learning through hands-on coaching and on-the-floor engagement
  • Champion a strong site-wide contamination control culture where prevention is everyone's responsibility
  • Provide governance-level oversight of contamination-related data, driving continuous improvement and reduction of repeat deviations
  • Act as the contamination control SME during client audits and regulatory inspections

Requirements

  • Degree in Microbiology, Biology, Biochemistry, Chemical Engineering or related discipline (Master's preferred)
  • Extensive industry experience in sterile or biologics pharmaceutical manufacturing, ideally within a CDMO
  • Strong expertise in aseptic processing, cleanroom operations and microbiological contamination control
  • Proven experience leading FMEA and cross-functional risk assessments
  • Solid understanding of global regulatory expectations
  • Ability to influence in matrixed environments with strong communication, coaching and facilitation skills

Nice to have

  • Hands-on involvement with EU GMP Annex 1 implementation
  • Experience supporting tech transfer into commercial manufacturing
  • Regulatory inspection and client audit readiness experience
  • Background in facilities operating shared equipment or campaign manufacturing

What we offer

  • Excellent salary and benefits package including enhanced pension, healthcare and annual bonus scheme
  • A chance to make a real difference and lead from the front in a key role on site
  • Working at the forefront of the biologics industry

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  • Embed contamination control principles into facility and equipment design, process flows, cleaning and sterilisation strategies, supplier management and training programmes
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  • Translate risk into practical, executable operational controls and maintain assessments as living tools informed by data and trends
  • Design and deploy contamination control training tailored to a CDMO environment, reinforcing learning through hands-on coaching and on-the-floor engagement
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  • Provide governance-level oversight of contamination-related data, driving continuous improvement and reduction of repeat deviations
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