Quality Assurance CSV Specialist

Start date: 14.01.2026Duration: 12 monthsLocation: VispHome office option: yes, 2 days home office possibleFor our Pharma client, we are looking for an experienced QA CSV Specialist, with minumum 5 years of experience in the Pharma industryMain responsibilities:Identify or create industry best practices and implement these within the framework of existing GAMP regulationsImplementing continuous improvements, procedures and local Validation Plans and Master Plans to ensure the department is operating as efficiently as possible by eliminating activities that do not positively impact production capacity or complianceDeveloping a project scope, implementation plan and tracking mechanisms, while being forward looking to identify roadblocks and solutions prior to issues affecting the project schedule.Actively audit projects and systems to ensure that the appropriate validation activities are carried out and are in compliance with regulatory requirements & corporate standardsIn conjunction with engineering, automation, operations and other departments, evaluate new applications in order to identify validation requirements.Act on behalf of, or be a conduit to, the QA CSV Manager on CSV issues to ensure that GMP issues are identified and addressed timely and correctly.Your experience:Bachelors degree in Engineering, Information Technologies, Natural Sciences or related.Fluent in English required, German is an advantage.Minimum 5 years experience in the Pharma industryExperience and in-depth understanding of all system lifecycle deliverables from Commissioning & Qualification (C&Q) and Computer System Validation (CSV) documents through System Retirement, as well as the regulatory requirements applicable (GMP Annex 11, 21CFR, GAMP, PICS...).