×
Register Here to Apply for Jobs or Post Jobs. X

Cleaning Validation Engineer

Job in Devon and Torbay, Torquay, Devon, TQ2, England, UK
Listing for: R&D Partners
Full Time position
Listed on 2026-10-11
Job specializations:
  • Quality Assurance - QA/QC
  • Pharmaceutical
    Pharma Engineer, Pharmaceutical Manufacturing
Salary/Wage Range or Industry Benchmark: 75000 - 95000 GBP Yearly GBP 75000.00 95000.00 YEAR
Job Description & How to Apply Below

Are you a Cleaning Validation expert ready to take ownership of complex automated washer systems and drive them to full GMP compliance?

R&D Partners is seeking a Cleaning Validation Engineer to lead and execute cleaning validation activities for large automated washing equipment at a pharmaceutical manufacturing site. This role requires an experienced professional who can independently assess the current validation status, identify gaps, and bring the system up to GMP standards. The position is fully onsite and offers an immediate start.

Please note that to be considered for this role you must have the right to work in this location.

Responsibilities:

  • Lead cleaning validation activities for large automated washers.
  • Review existing validation approaches and identify outstanding gaps or challenges.
  • Update and improve validation procedures, SOPs, and cleaning recipes/cycles.
  • Independently drive validation activities through to completion.
  • Collaborate closely with the site's operational validation team.
  • Coordinate activities and manage deliverables, requiring strong project management and stakeholder management skills.
  • Ensure documentation and validation activities meet pharmaceutical GMP requirements.
  • Support the eventual handover of the validated system to the operational validation team.

Key Skills and Requirements:

  • Approximately 7-10 years of pharmaceutical validation experience.
  • Strong specialist knowledge of cleaning validation and automated washers.
  • Proven ability to work independently and take ownership of complex validation projects.
  • Excellent project management and stakeholder coordination skills.
  • Familiarity with GMP requirements and documentation standards.

For more information, please contact Jack Keens.

To View & Apply for jobs on this site that accept applications from your location or country, tap the button below to make a Search.
(If this job is in fact in your jurisdiction, then you may be using a Proxy or VPN to access this site, and to progress further, you should change your connectivity to another mobile device or PC).
 
 
 
Search for further Jobs Here:
(Try combinations for better Results! Or enter less keywords for broader Results)
Location
Increase/decrease your Search Radius (miles)
0
200
Filters
Education Level
Experience Level (years)
Posted in last:
Salary