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Production Operator – Cleanroom Manufacturing

R&D Partners · Tipperary

New
🇬🇧 English
cGMP cGDP

Job description

About the role

Join a dynamic manufacturing team in a regulated cleanroom environment, supporting the production of innovative pharmaceutical products. The role involves maintaining high‑quality standards, adhering to safety protocols, and working on rotating day and night shifts.

Key responsibilities

  • Follow and promote workplace safety and environmental health practices.
  • Report safety, quality, equipment, or material issues to the appropriate manager.
  • Assist with the introduction of new products, equipment, and procedures, creating necessary documentation.
  • Collaborate with team leads to prioritize tasks and meet production schedules.
  • Complete and report employee training to ensure compliance with quality standards.
  • Maintain accurate timesheets and record hours for R&D reporting.
  • Apply problem‑solving skills to resolve production challenges and support continuous‑improvement initiatives.
  • Keep the workspace clean and organized, following a “clean as you go” policy.
  • Ensure compliance with cGMP and cGDP regulations.

Required profile

  • Proven experience as a production operator in a GMP environment.
  • Strong commitment to safety, quality, and cleanroom attire.
  • Ability to follow detailed instructions and complete documentation accurately.
  • Effective teamwork and problem‑solving abilities.
  • Flexibility to work rotating day and night shifts.

Required skills

  • cGMP (current Good Manufacturing Practices)
  • cGDP (current Good Documentation Practices)

What we offer

  • Shift allowance for day and night schedules.
  • Opportunities to work on cutting‑edge pharmaceutical projects.
  • Supportive team environment with continuous‑improvement focus.

Questions fréquentes

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Published 1 week ago

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R&D Partners

Tipperary