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Validation Specialist x 2 (Pharma)

Job description

This global biopharmaceutical leader wants two ambitious, driven and experienced Validation professionals to join their Technical department in their Cork branch.

JOB RESPONSIBILITIES

  • Ensuring highest Quality, Compliance and Safety standards are adhered to.
  • Validation protocol/report authoring/execution/oversight/approval as appropriate.
  • Recommending technical approaches in line with global and local standards.
  • Conducting detailed technical assessments of materials and supplier changes and proactively manage the implementation of changes.
  • Maximizing team member performance through continuous process improvement initiatives.
  • Benchmarking and remaining current with development of new technologies 
  • Participating in problem solving teams across all areas of the Deparment
  • Supporting process related deviations and reports.

JOB REQUIREMENTS

  • 4+ years’ experience in a regulated manufacturing environment.
  • Knowledge of cleaning validation and CIP systems,
  • Knowledge of material qualification and supplier change notifications.
  • Knowledge of temperature mapping activities, requalification requirements of equipment, periodic reviews of equipment
  • Knowledge of the requirements around sanitization and sterilization processes.
  • Hon. Degree or Masters in a Science or Engineering discipline.

For a confidential discussion on this or any other current job opportunity please contact Marcel Skolimowski on 021 4847 138 / marcel@sigmar.ie

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