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Ready to put your cGMP expertise and attention to detail to work in a hands-on pharmaceutical manufacturing environment?

º¬Ðß²ÝÓ°Ôº is seeking a Manufacturing Associate (Level III) to support daily manufacturing operations in a cGMP environment. This role focuses on ensuring compliance, maintaining equipment and facilities, and contributing to the production of high-quality pharmaceutical products. The position requires attention to detail, strong documentation skills, and collaboration with other site functions.

Please note that to be considered for this role you must have the right to work in this location or hold an EU passport.

Responsibilities:

• Perform and document daily manufacturing operations in a cGMP environment.
• Operate process equipment and execute validation protocols.
• Revise and maintain cGMP documents to ensure compliance.
• Maintain equipment and facilities to required standards.
• Support other functions on-site as needed.
• Ensure training levels are maintained to meet operational requirements.

Key Skills and Requirements:

• Strong attention to detail and documentation skills.
• Familiarity with cGMP standards and manufacturing processes.
• Ability to operate and maintain manufacturing equipment.
• Collaborative mindset to support cross-functional teams.
• Commitment to maintaining compliance and quality standards.

If you are having difficulty in applying or if you have any questions, please contact Joshua Bye at j.byej.bye@proclinical.com.

Apply Now:

If you are interested in applying to this exciting opportunity, then please click 'Apply' or to speak to one of our specialists please request a call back at the top of this page.

º¬Ðß²ÝÓ°Ôº is a leading life sciences recruiter focused on finding exceptional people and matching them with the finest positions across the globe. º¬Ðß²ÝÓ°Ôº is acting as an Employment Agency in relation to this vacancy.

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