Description
The Validation Engineer will be responsible for the performance and execution of Production and Cleaning Validation. The primary focus of the role will be on validation transfers of existing products to new equipment within the site.Key duties and Responsibilities:
- Responsibility for the co-ordination of Process Validation, Cleaning Validation activity and Equipment Validation in the Production Department.
- Preparation and execution of validation and re-validation protocols and reports, (IQ / OQ / PQ), for the validation of equipment, systems, products and projects.
- Responsible for Investigating and resolving deviations associated with validation studies.
- Acting as the primary point of contact for all Production related Validation matters as well as internal and external compliance audits or regulatory inspections.
Applicants should have a third level degree or equivalent in a Pharmacy/Science/Engineering discipline with a minimum of two years validation experience in the Pharmaceutical industry.
Demonstrated Validation experience in Granulation, Tabletting and Coating areas would be beneficial.
This role will have a start date of August and provides competitive hourly rates. If you would like to apply please contact Sarah Irvine on or apply with a copy of your current CV.
We also provide vouchers for any successful referrals so if you know of anyone who may be looking please feel free to get in touch.