Manufacturing Associate III für Swisslinx AG in Solothurn - myjob.ch
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      06.09.2026

      Manufacturing Associate III

      • Solothurn
      • Festanstellung 100%

      • Merken
      • drucken
       

      Swisslinx AG

      Swisslinx AG

      Manufacturing Associate III

      You will support daily manufacturing activities within a cGMP-regulated production environment, ensuring that operations are performed safely,…

      Manufacturing Associate III

      Job description:

      You will support daily manufacturing activities within a cGMP-regulated production environment, ensuring that operations are performed safely, accurately and in compliance with applicable quality standards and procedures.

      About the customer:

      • Role: Manufacturing Associate III
      • Location: Solothurn
      • Start: ASAP until 28/02/2027 with possible extension
      • Workload: Full time

      Requirements:

      • Perform and document daily manufacturing operations in accordance with cGMP requirements.
      • Operate manufacturing and process equipment.
      • Support the execution of validation protocols and related manufacturing activities.
      • Review and revise cGMP documentation where required.
      • Ensure compliance with cGMP standards, internal procedures and quality requirements.
      • Support the maintenance of manufacturing equipment and facilities.
      • Maintain the required level of training and ensure all assigned training is completed on time.
      • Collaborate with and support other functions across the site as needed.
      • Contribute to the smooth and efficient running of daily manufacturing operations.
      • Maintain accurate and complete documentation throughout all manufacturing activities.

      Competences:

      • 3–5 years of relevant experience within pharmaceutical, biotechnology or another cGMP-regulated manufacturing environment.
      • Hands-on experience supporting manufacturing operations and operating process equipment.
      • Good understanding of cGMP requirements and compliant documentation practices.
      • Experience supporting validation activities and working with validation protocols.
      • Strong attention to detail and very good documentation skills.
      • Ability to work reliably within established procedures and quality systems.
      • Comfortable working collaboratively with different functions across a manufacturing site.
      • Strong sense of responsibility and commitment to maintaining a safe and compliant working environment.

      Arbeitsort: Solothurn