Senior CIP & Cleaning Validation Lead - On-site Pharma

Korn Ferry Group

Region Sjælland

On-site

DKK 700,000 - 1,000,000

Full time

9 days ago

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Job summary

Senior Cleaning Validation / CIP Specialist in Zealand, Denmark, on-site, requires 8+ years of dedicated CIP experience and fluency in English. You will lead cleaning validation strategies, perform MACO calculations, and document IQ/OQ/PQ while coordinating with QA, Engineering and Production teams on challenging, regulated manufacturing projects.

Ideal candidates have a background in pharmaceuticals, biotechnology, or related fields and can independently own validation activities on-site,

Qualifications

  • 8+ years of dedicated CIP experience required.
  • Strong background in cleaning validation and CIP systems.
  • Experience in pharmaceuticals, biotechnology, food manufacturing or medical devices.

Responsibilities

  • Develop and implement cleaning validation strategies.
  • Plan and execute cleaning validation activities.
  • Perform cleaning risk assessments and MACO calculations.
  • Define CIP system requirements and support system design.
  • Plan and conduct riboflavin spray-coverage testing.
  • Prepare IQ, OQ and PQ protocols and reports.
  • Investigate deviations and perform root‑cause analysis.
  • Troubleshoot cleaning and CIP‑related issues.
  • Optimize CIP cycles to reduce cycle time and boost efficiency.

Skills

CIP experience
Cleaning validation
MACO calculations
Documentation
Regulatory knowledge
Risk assessment
On-site work

Education

Engineering/Pharmacy/Biotechnology degree

Job description

Senior Cleaning Validation / CIP Specialist in Zealand, Denmark, on-site, requires 8+ years of dedicated CIP experience and fluency in English. You will lead cleaning validation strategies, perform MACO calculations, and document IQ/OQ/PQ while coordinating with QA, Engineering and Production teams on challenging, regulated manufacturing projects.

Ideal candidates have a background in pharmaceuticals, biotechnology, or related fields and can independently own validation activities on-site,

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