Senior Validation Specialist

ROLE OVERVIEW We are supporting a leading Pharmaceutical company who are seeking a Senior Validation Specialist to join their team in the Essex area. As the Senior Validation Specialist, you will play a crucial role in ensuring that all GMP processes, equipment, and computerised systems meet regulatory and business requirements. KEY DUTIES AND RESPONSIBILITIES: Your duties as the Senior Validation Specialist will be varied however the key duties and responsibilities are as follows: 1. Provide ongoing engineering validation support for GxP processes, equipment and computerised systems across the site. 2. Act as a subject matter expert in EU and FDA regulations, ensuring compliance with validation policies and procedures. 3. Review and approve validation documentation, ensuring timely and compliant submissions. 4. Support QMS activities, including deviation investigations and change control impact assessments. ROLE REQUIREMENTS: To be successful in your application to this exciting role as the Senior Validation Specialist we are looking to identify the following on your profile and past history: 1. Relevant degree in Engineering, Sciences, or equivalent. 2. Extensive industry experience in engineering validation, with a focus on computer system validation. 3. A working knowledge and practical experience with GxP regulations and guidelines. Key Words: Senior Validation Specialist / GxP / Computer System Validation / Engineering Validation / Life Sciences / Regulatory Compliance / QMS / EU Regulations / FDA Regulations / Validation Documentation / Deviation Investigations Hyper Recruitment Solutions Ltd (HRS) is an Equal Opportunities employer. We welcome applications from anyone who meets the role requirements. HRS exclusively supports the Life Science sectors, combining recruitment expertise with scientific knowledge to help you advance your career.

Location: Essex, UK, GB

Posted Date: 10/31/2025