Validation Technician

Validation Technician

Location:

Braunton, GB, EX33 2DL

Join Perrigo, a leader in consumer self‑care and a top player in the European market. Our mission is to make lives better through trusted health and wellness solutions that are accessible to all.

• Prepare and execute validation protocols based on master plans and schedules in Process Validation, including Performance Qualification, product hold time and transport studies, Equipment Qualification, Cleaning Validation, Computer Systems Validation, Spreadsheet Validation, and temperature profile mapping for quality critical equipment.
• Conduct periodic lifecycle reviews for each validation discipline.
• Support improvement projects with technical input and participate in problem‑solving teams such as CAPA, Quality Event, and Kaizen.

• Generate and assist in the completion of qualification and validation protocols to enable compliant and efficient introduction of new or changed products, processes, equipment, computer systems, spreadsheets, and cleaning procedures.
• Report results and findings following protocol execution.
• Conduct lifecycle reviews for products, processes, equipment, cleaning processes, computer systems, spreadsheets, and temperature profiles for quality‑controlled equipment.

• Collaborate with Quality Engineering and Operational Excellence to provide validation and qualification expertise in improvement initiatives.
• Provide data via validations to support product control plans and risk assessment processes.
• Take an active role in CAPA action teams, QE investigation teams, and Kaizen events when required.

• Identify validation and qualification requirements through risk assessment for both new and changed products, processes, equipment, cleaning procedures, computer systems, and spreadsheets.

• Undertake other reasonable duties as required to support the Perrigo business.

• Flexibility to work varied hours as needed, though this is not expected to be frequent.
• Minimum of 2 years’ experience in validation or process engineering roles within the pharmaceutical or other regulated industry.
• Knowledge of GMP and its application in validation and change management, and ability to learn new regulations.
• Preferred experience in a lean management environment, though not essential.

Competitive compensation, comprehensive benefits for you and your family, and career development opportunities to ensure you feel valued and supported both professionally and personally. Learn more about Perrigo's Total Rewards and our recognition as a Forbes “America’s Best Employers by State 2024”.

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We are an equal opportunity employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, status as a protected veteran, or other characteristics protected by law.