We are currently looking for a Validation Specialist to join a leading pharmaceutical company based in the East Sussex area. As the Validation Specialist, you will be responsible for KEY DUTIES AND RESPONSIBILITIES: Your duties as the Validation Specialist will be varied however the key duties and responsibilities are as follows: 1. Effectively leading the execution of validation projects. 2. Providing commissioning, qualification, and validation support to new and ongoing projects across the site. 3. Ensuring validation and revalidation requirements are identified and implemented. 4. Confirming that all required processes and/or equipment remain in a validated state in accordance with company policy and regulatory requirements. ROLE REQUIREMENTS: To be successful in your application to this exciting role as the Validation Specialist we are looking to identify the following on your profile and past history: 1. Relevant degree in an Engineering or Science discipline. 2. Proven industry experience in a quality (validation) environment within the pharmaceutical industry. 3. A working knowledge and practical experience with Good Manufacturing Practice (GMP). Key Words: Senior Validation Engineer / Validation / Project Management / Pharmaceutical / GMP / Quality Assurance / East Sussex/ Commissioning / Qualification / Compliance / Risk Management Hyper Recruitment Solutions Ltd (HRS) is an Equal Opportunities employer. We welcome applications for any applicant who fulfill the role requirements for this position. HRS is a company exclusively supporting the science and technology sectors, and is made up of a collaboration of recruitment professionals and scientists. We look forward to helping you with your next career moves.