Production Operator – Cleanroom Manufacturing
R&D Partners · Tipperary
Description du poste
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.
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R&D Partners
Tipperary
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