Cleanroom Production Operator – Pharmaceuticals

Are you ready to turn precision into progress and play a key role in shaping the future of pharmaceutical innovation?

R&D Partners is seeking a dedicated and experienced Production Operator to join a dynamic manufacturing team within a cleanroom environment. In this role, you will play a key part in ensuring smooth production processes, maintaining high-quality standards, and adhering to safety protocols. This position includes shift work with an additional allowance.

Please note that to be considered for this role you must have the right to work in this location.

Shift information: 

• Day shift: 7:00am – 7:00pm
• Night shift: 7:00pm – 7:00am

Shifts rotate weekly – one week of days, one week of nights, followed by a split shift (two day shifts, one day off, then two night shifts). The client operates Monday through Friday. For those working the Friday night shift, it ends at 4:00am on Saturday.

Responsibilities:

• Follow and promote workplace safety and environmental health practices.
• Report any issues related to safety, quality, equipment, or materials to the appropriate manager.
• Assist in introducing new products, equipment, and procedures while developing necessary documentation.
• Collaborate with team leads to prioritize tasks and meet production schedules.
• Complete and report on employee training to ensure compliance with quality standards.
• Maintain accurate timesheets and submit them for review weekly.
• Record and report hours worked for research and development purposes.
• Use problem-solving skills to address and resolve production challenges.
• Work closely with support teams to resolve operational issues.
• Meet daily production goals and participate in team communication.
• Ensure all training is completed efficiently and maintain compliance with training requirements.
• Support continuous improvement initiatives and lean manufacturing practices.
• Maintain cleanliness and organization in the workspace, adhering to a “clean as you go” policy.
• Follow all documented policies, procedures, and regulatory requirements.
• Ensure compliance with Good Manufacturing Practices (cGMP) and Good Documentation Practices (cGDP).
• Represent the company professionally during client or regulatory interactions.
• Participate in investigations and assist in resolving any identified issues.

Key Skills and Requirements:

• Proven years of working experience as a production operator in a GMP environment is a must.
• Strong commitment to workplace safety and quality standards.
• Willingness to wear appropriate cleanroom gowns to ensure compliance with quality standards.
• Ability to follow detailed instructions and complete required documentation accurately.
• Effective problem-solving and teamwork skills.
• Willingness to participate in training and continuous improvement efforts.
• Flexibility to work shifts and adapt to changing priorities.

For more information, please contact Billy O’Brien.

If you are interested in applying to this exciting opportunity, then please click ‘Apply’ or to speak to one of our specialists visit the ‘Contact Us’ page.

R&D Partners is a leading life sciences recruiter focused on finding exceptional people and matching them with the finest positions across the globe. R&D Partners is acting as an Employment Agency in relation to this vacancy.

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