Senior Manufacturing Associate (Downstream and Upstream Processing)

Randstad Switzerland; Luterbach; Vor Ort; CHF 100.000 - 130.000; Vollzeit

Zusammenfassung

Randstad Switzerland represents a leading biotechnology client in Luterbach, Solothurn, seeking a Senior Manufacturing Associate in Downstream and Upstream Processing. The role involves hands-on daily GMP operations, equipment handling, and meticulous documentation in a cGMP environment.

You bring 3–5 years of GMP pharma/biotech experience, familiarity with either downstream or upstream processing, strong attention to detail, and English communication at least at level B1.

Qualifikationen

• 3–5 years of GMP experience in pharma/biotech.
• Experience in downstream or upstream processing.
• English communication at least level B1.
• Excellent documentation and attention to detail.

Aufgaben

• Performs and documents daily manufacturing operations in a cGMP environment, operating process equipment and executing validation protocols.
• Ensures compliance to cGMP and maintains equipment and facilities on site.
• Maintains training level and supports other functions on site.
• Assists with daily manufacturing operations in the facility.

Kenntnisse

GMP knowledge

Documentation

Attention to detail

Team collaboration

Jobbeschreibung

For our client, a leading biotechnology company, we are seeking a Senior Manufacturing Associate in Downstream and Upstream Processing.

General Information:

• End date: 28.02.2027
• Extension: to be discussed
• Workplace: Luterbach, Solothurn

Tasks & responsibilities:

• Performs and documents daily manufacturing operations in a cGMP environment including operation of process equipment, execution of validation protocols, revising cGMP documents.
• Ensuring compliance to cGMP as well as maintaining equipment and facilities.
• Maintaining training level to the required level and support other functions on site.
• Assists with daily manufacturing operations in manufacturing facility.

Requirements:

• 3-5 years of relevant experience in GMP, ideally in pharma or biotech environment
• Experience in either in Downstream or Upstream Processing
• Good communication skills in English, at least level B1
• Attention to details with strong documentation skills