Validation Specialist | Pharmaceutical | Kent | Permanent | up to £55,000 DOE
Are you a Validation Specialist with a passion for cleaning validation, GMP compliance, and equipment qualification? Join a leading pharmaceutical company where your work will directly contribute to safe, high-quality pharmaceutical production.
What You'll Do:
1. Execute validation protocols (IQ/OQ/PQ/PV) for equipment, facilities, and processes
2. Cleaning validation activities, develop protocols, sampling strategies, set limits, and compile reports
3. Perform temperature mapping and requalification of GMP-critical equipment
4. Draft and maintain validation documentation, including master plans and SOPs
5. Collaborate closely with QA, Engineering, and Production to ensure compliance with minimal disruption
6. Support internal and external audits and inspections
7. Stay current with regulatory guidelines (Annex 15, ISO 13485, EudraLex Vol 4) and drive process improvements
What You'll Bring:
1. 2+ years' validation experience in a GMP-regulated pharmaceutical environment
2. Hands-on experience with cleaning validation, including protocol writing and execution.
3. Knowledge of Annex 11, Annex 15, ISO 9001, and ISO 13485
4. Familiarity with calibration principles, validation lifecycle, and documentation standards
5. Strong written and verbal communication skills
6. Proficient in Microsoft Word, Excel, and PowerPoint
7. Highly organised, detail-oriented, and proactive
Why Apply?
1. Join a well-established pharmaceutical company known for quality and innovation
2. Great benefits packages that includes Annual Incentive Plan, Private Medical Insurance and Life Assurance
3. Be part of a supportive, collaborative team environment
4. Play a key role in high-impact projects that matter
5. Benefit from professional development opportunities and a structured career path
#J-18808-Ljbffr