We are looking for for an experienced Validation Engineer to join our laboratories in Glasgow and Newhouse.
This is a great opportunity for an experienced Validation Engineer to join our laboratories in Glasgow and Newhouse. You will be a key member of the team, leading the execution and documentation of validation activities performed during the qualification of facilities, utilities and equipment.
You will be collaborating with colleagues, external partners and suppliers. Your role will include working to EU GMP Annex 11, 21 CFR Part 11, GAMP 5 and associated computerised system validation within the pharmaceutical environment.
What you will accomplish together with us:
Primary contact and validation subject matter expert
Working within the guidelines of GMP
Ensuring all work is performed within production time constraints
Owning and developing validation master plan and relevant documentation
Responsible for authoring, executing, reporting and testing IQ, OQ and PQ validation activities within project timescales
Managing multiple validation projects |equipment, facilities, utilities, including associated control systems
Acting as a subject matter expert in customer and regulatory audits
Working collaboratively with the project team and various departments
Responsible for the generation of accurate protocols and reports
What will convince us:
Educated to HND in a scientific or engineering discipline or equivalent
IQ, OQ and PQ equipment validation and testing experience within the pharmaceutical or medical device industry
A sound understanding of pharmaceutical technology and its respective validation requirements