Pharmaceutical Validation Specialist

13 hours ago

Cork, Cork, Ireland beBeeValidation Full time €70,000 - €95,000

Job Title: Validation Specialist

A dynamic and experienced Validation Specialist is required to join our team for a 12-month contract. This role involves the validation of all new computerized equipment, control systems, and manufacturing processes.

Key Responsibilities:

  • Develop and execute validation protocols for computerized equipment and systems.
  • Participate in the change control process advising on CSV issues.
  • Manage DQ, IQ, OQ, and PQ activities ensuring compliance with cGMP regulations.
  • Provide technical assistance on current US FDA and EU validation requirements.
  • Ensure that the validation status of equipment and systems are in compliance with cGMP at all times.

Requirements:

  • Degree in Science (Chemistry, Microbiology, or Pharmacy) or Engineering (Chemical, Mechanical, or Electrical).
  • 3-5 years experience working in a Healthcare manufacturing environment – ideally part of which would be in the pharmaceutical sector.
  • 2-3 years experience in validation environment.

Benefits:

  • Initially 100% onsite; after the first few months, up to two days per week remote working may be possible (on one of the working days needs to be Monday or Friday).

Role Overview:

This role requires a strong understanding of validation principles, regulatory requirements, and good manufacturing practices (cGMP). As a key member of our team, you will work closely with colleagues to ensure the delivery of high-quality products while maintaining compliance with regulatory standards.

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