Senior Manufacturing Operator, cGMP & Compliance

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

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.