Sunday Times Best Places to Work 2024 BioNow Business Growth Award Winner 2024 The Opportunity: We are seeking a highly skilled and experienced Validation Specialist who’s primary purpose will be to validate equipment, systems, processes, facilities, and utilities. Key Accountabilities Writing/approving GMP documentation including (but not limited to) protocols, reports, URSs, FATs, SOPs, BMRs, HACCPs and other technical or scientific supporting documents Executing validation protocols Investigating and writing deviations or non-conformance reports Performing and writing risk assessments Performing and writing root cause analyses Ensuring all relevant items are qualified/validated within the planned dates Involvement in audits both from internal and external parties Keeping up to date with current regulatory requirements Skills, Qualifications and Experience Essential To be successful in this role, applicants need to have the following essential skills and experience: Validation experience of several the following: equipment, systems, processes, facilities, utilities, etc Experience of working within a pharmaceutical or related GMP environment Demonstrated written and oral communication skills Demonstrated ability to work well as part of a team Experience of IT programmes (e.g., Microsoft office, document management or other relevant programmes) Demonstrated planning / organisational skills and the ability to work under their own initiative. Desirable Experience of laboratory equipment qualification Experience of cold chain qualification Do you want to feel inspired every day? We are future-focused, and our business is growing rapidly. We succeed together through passion, commitment, and teamwork, and so can you.