
Pharmaceutical Validation Specialist
1 week ago
We are seeking a skilled professional to lead validation activities for computerised equipment and systems in a sterile manufacturing environment.
- The ideal candidate will be responsible for generating validation documentation and executing protocols, as well as participating in change control processes.
- They will also contribute to the development and execution of DQ, IQ, OQ, and PQ protocols, ensuring all projects are delivered in line with cGMP, Health & Safety, environmental, and regulatory standards.
Candidates should possess strong technical knowledge of pharmaceutical operations and familiarity with GAMP, ISPE Baseline Guides, and quality/compliance regulations.
Requirements:- Degree in Science (Chemistry, Microbiology, or Pharmacy preferred) or Engineering (Chemical/Mechanical/Electrical).
- Post-graduate qualification desirable.
- 3–5 years' experience in a healthcare manufacturing environment, ideally within the pharmaceutical sector.
- 2–3 years' experience in a validation or CSV role.
- Project management experience.
- Effective communication and facilitation skills, with ability to influence and work across multifunctional teams.
In addition to a competitive compensation package, we offer opportunities for professional growth and development.
Why Choose Us?We value our employees and strive to create a diverse and inclusive workplace where everyone is respected and supported.
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