Hands-On cGMP Manufacturing Associate (Level III)

Proclinical Staffing; Bezirk Solothurn; Vor Ort; CHF 70.000 - 100.000; Vollzeit

Zusammenfassung

Proclinical Staffing is seeking a Manufacturing Associate (Level III) to support daily manufacturing operations in a cGMP environment. You will help ensure compliance, maintain equipment and facilities, and contribute to the production of high-quality pharmaceutical products.

This role requires strong documentation skills, attention to detail, and collaboration with cross-functional site teams to uphold 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

Collaborative mindset

Cross-functional teamwork

Jobbeschreibung

Proclinical Staffing is seeking a Manufacturing Associate (Level III) to support daily manufacturing operations in a cGMP environment. You will help ensure compliance, maintain equipment and facilities, and contribute to the production of high-quality pharmaceutical products.

This role requires strong documentation skills, attention to detail, and collaboration with cross-functional site teams to uphold quality standards.