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Manufacturing Operator Biotech (w/m/d)

  • Locatie:

    Wallis, Zwitserland

  • Contactpersoon:

    Melis Bartsch

  • Contractsoorten:

    Temp to Perm

  • Telefoon contactpersoon:

    +41 41 749 49 19

  • Bedrijfssectoren:

    Biotechnology

  • E-mail contactpersoon:

    melis_bartsch@oxfordcorp.com

About the Client

Our client is a major player in the pharmaceutical manufacturing sector, known for its advanced drug product facilities in Switzerland. Their site specializes in producing liquid and lyophilized drug forms, supporting a wide range of therapies for global markets. With a strong focus on innovation, quality, and compliance, they offer a collaborative and high-performing environment for professionals seeking to advance their careers in the biotech and pharmaceutical industries.

Job Description

We are looking for a Manufacturing Operator in the Biotech area to support the production of sterile drug products, including liquid and freeze-dried forms, at our client's site in Switzerland. This role involves operating, setting up, and cleaning production equipment in compliance with cGMP standards. You will contribute to smooth batch execution, troubleshoot issues, and ensure accurate documentation to maintain product quality. This is a hands-on position for individuals with strong technical skills and a commitment to high standards in pharmaceutical manufacturing.

Responsibilities

  • Operate, clean, and set up production equipment for sterile drug product manufacturing

  • Perform manufacturing activities according to cGMP standards and batch records

  • Monitor processes and troubleshoot equipment issues, proposing solutions as needed

  • Complete and review production documentation in a timely and accurate manner

  • Support investigations and assist with decision-making on production issues

  • Contribute to process changes, CAPAs, and continuous improvement projects

  • Train and guide colleagues and new team members in relevant procedures

  • Maintain a safe, organized, and compliant work environment at all times

Requirements

  • 2-4 years of experience in GMP-regulated pharmaceutical manufacturing (preferably in sterile drug products)

  • Strong understanding of cGMP principles, quality procedures, and SOPs

  • Ability to communicate effectively in English or German (both is a plus)

  • Team player with a proactive and structured work approach

  • Experience with equipment setup, troubleshooting, and cleaning processes

  • Comfortable working in a 2-shift pattern with flexibility

  • IT skills, including SAP and MES, are an advantage

  • High motivation and willingness to contribute to a dynamic team environment