Validation Specialist
- Newcastle
- £38,000-42,500 per year
- Permanent
- Part-time
- Lead validation activities for the introduction of new facilities, equipment, systems, processes, products, and technologies.
- Generate and control validation documentation (URS, FAT/SAT, FDS, DQ, IQ, OQ, PQ, and validation reports).
- Maintain site validation status, ensuring all assets remain in a validated state.
- Prepare validation plans, protocols, and reports for equipment, systems, and software.
- Conduct validation studies and develop project scopes aligned with business needs.
- Manage the site's Validation Master Plan.
- Act as subject matter expert for validation and qualification activities.
- Liaise with customers for new product introductions and re-validations.
- Support ongoing process verification activities and ensure timely completion of CAPAs and change controls.
- Proven experience in validation within a GMP-regulated pharmaceutical or life sciences environment.
- Strong understanding of the full validation lifecycle and regulatory requirements.
- Experience with Computer Systems Validation.
- Confident in Microsoft Office applications.
- Excellent communication skills and the ability to work both independently and as part of a team.
- Scientific or engineering degree (or equivalent industry experience).
- Willingness to travel domestically and internationally as required.