Description
Validation Engineer - Secondary PharmaceuticalsType - initially 6 month contract
Location - UK, South
One of our global Pharmaceutical leaders is looking for a couple of Validation Professionals to join their team on an ongoing project, at their Secondary Manufacturing plant.
Key Responsibilities
• Validation documentation - drafting, reviewing and approving validation documentation IQ, OQ, PQs and protocols
• Preparation and writing of the Validation Master Plan
• Accountable for scheduling, tracking, reporting and achieving project deadlines
• Co-ordinate the execution of re-qualification
• Attend departmental and team meetings focused on Qualification / Validation activities.
• Understanding and applying industry specific compliance standards/regulations to all Qualification / Validation activities.
• Developing an understanding of the importance, considering impact on GMP and compliance, on decisions made.
Key Experience:
• Experience in validation of pharmaceutical secondary manufacturing equipment such as blenders/mixers/isolators/ powder filling etc
• Additional experience in utilities and/or clean rooms would be also beneficial
• Strong technical writing and communication skills
• Must be goal-oriented and able to prioritise and manage risks