Job Ref: 2905 Recruiter: Tom Doyle
Country: Ireland Location: Dublin
Job Category: Process, Pharma Life Science, Salary Range: €Negotiable

Job Description

Validation Engineer (Cleaning Validation) Pharmaceutical Process Plant Dublin West.  kppm are looking to recruit a Validation Engineer for our client based in West Dublin

The Job: You will be responsible for aspects of the Cleaning Validation programmes onsite at the FGMIE manufacturing site in Dublin.

Suitable Candidates: Will have  degree in a life-science / engineering related discipline and strong experience in cleaning validation (minimum of 3 year’s validation experience). Experience and a good understanding of the pharmaceutical industry including GMP and relevant validation requirements. You will be a self-starter, possessing excellent interpersonal, team work and communication skills. You will have a demonstrated track record in the delivery of goals and improvements. You will have had experience of working to tight deadlines.

Furthermore you will be:

  • passionate and enthusiastic in your way of working
  • a professional with positive and proactive influencing and collaboration skills
  • a strong and proactive team player who thrives on working in a fast paced production environment.
  • possess strong attention to detail.

Primary Tasks of the role:

  • Co-ordinate cleaning validation site wide including worst case studies.
  • Co-ordinate and execute Cleaning Validation studies.
  • Liaise with Planning, Production and Laboratories to coordinate these studies.
  • Generate Protocols / Reports / SOPs / WIs associated with cleaning validation studies.
  • Perform Sprayball coverage or Riboflavin testing for new equipment.
  • Input into APQR and OCV reports.
  • Participate in Change control assessments and deviation investigations relating to cleaning.
  • Participate in preparation and presentation of Cleaning Validation data during regulatory audits
  • Ensure work is carried out in accordance with the requirements of Company Group Validation Policies, Guidelines, Site Validation Master Plan and GMP.

For further information or to apply in strictest confidence please contact:Tom Doyle at kppm,  P: 086 8205038.  E:

or email

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