Proclinical are seeking a dedicated Validation Engineer to ensure the ongoing validation and compliance of equipment, systems, and processes in a healthcare manufacturing environment.
Responsibilities:
- Design, execute, and report on validation studies for equipment, systems, and processes.
- Provide technical interpretation and guidance on current US FDA and EU validation requirements.
- Maintain validation documentation throughout the validation lifecycle and support site change control process.
Requirements:
- 3-5 years' experience in a healthcare manufacturing environment, ideally in the pharmaceutical sector.
- Strong technical knowledge of pharmaceutical plants and understanding of relevant quality and compliance regulations.
- Degree in Science (Chemistry, Microbiology, or Pharmacy preferred) or Engineering (Chemical/Mechanical/Electrical).
Proclinical is a specialist employment agency and recruitment business, providing job opportunities within major pharmaceutical, biopharmaceutical, biotechnology and medical device companies.
Proclinical Staffing is an equal opportunity employer.
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