Manufacturing Associate (level III)

Proclinical Group; Bezirk Solothurn; Vor Ort; CHF 65.000 - 90.000; Vollzeit

Zusammenfassung

Proclinical is seeking a Manufacturing Associate (Level III) to support daily manufacturing operations in a cGMP environment in Solothurn, Switzerland. This hands-on role focuses on ensuring compliance, maintaining equipment and facilities, and contributing to the production of high-quality pharmaceutical products.

The ideal candidate will have strong documentation skills, attention to detail, and the ability to collaborate with cross-functional teams while upholding strict quality standards.

Qualifikationen

• 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.

Aufgaben

• 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.

Kenntnisse

Attention to detail

Documentation skills

cGMP knowledge

Equipment operation

Collaborative mindset

Jobbeschreibung

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

Proclinical 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.

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