Cleaning Validation Engineer

Proclinical is working with a Global Pharmaceutical organisation who have an extensive history and heritage in developing innovative studies and general programmes. They are known for their passion for developing and manufacturing lifesaving drugs and distributing them around the world.

You will be responsible for aspects of the Cleaning Validation programs onsite at the state of the art manufacturing site in Dublin.

Role Overview:

• 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 validation studies.
• Preform Sprayball coverage or Riboflavin testing for new equipment.
• Input into APQR and OPV reports.
• Participate in Change control assessments and deviations investigation relate 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 the Group Validation Policies, Guidelines, Site Validation Master Plan and GMP

Skills and Requirements:

• Degree in the Life Science industry
• Extensive experience in cleaning and process validation with a minimum of 3 year's validation experience.
• You will be a self-starter, possessing excellent interpersonal, team work and communication skills

To Apply:

Please click on the Apply button. Please include a short note outlining why you are interested in the role and why you think you are suitable.
In case you have difficulty in applying or if you have any questions, please call Joseph Emmott on +44 203 8141 316 or upload your CV on our website - www.Proclinical.com.
A full job description is available on request.
Proclinical is a specialist employment agency and recruitment business, providing job opportunities within major pharmaceutical, biopharmaceutical, biotechnology and medical device companies.