Manufacturing Associate / Manufacturing Associate

Join Our Team as a Manufacturing Associate (Level III)

Are you ready to leverage your cGMP expertise and keen attention to detail in a dynamic pharmaceutical manufacturing environment? Proclinical is seeking a dedicated Manufacturing Associate (Level III) to support daily manufacturing operations in a compliant cGMP setting. This role emphasizes adherence to compliance standards, maintenance of equipment and facilities, and the contribution to the production of high-quality pharmaceutical products.

The ideal candidate will possess strong documentation skills and be able to collaborate effectively with other functions on-site. Please note that only applications matching the job profile will be considered. Additionally, applicants 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.

Apply online using the form below.

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