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01Compétences
02CollaborationAttention to detailProduction operationscGMPDelta validation protocolsQuality management systemSafety certificationTraining and DevelopmentGood Documentation Practices
Le poste
03Manufacturing Associate III
Location: Solothurn
Start: ASAP until 28/02/2027 with possible extension
Workload: Full time
01Perform and document daily manufacturing operations in accordance with cGMP requirements.
02Operate manufacturing and process equipment.
03Support the execution of validation protocols and related manufacturing activities.
04Review and revise cGMP documentation where required.
05Ensure compliance with cGMP standards, internal procedures and quality requirements.
06Support the maintenance of manufacturing equipment and facilities.
07Maintain the required level of training and ensure all assigned training is completed on time.
08Collaborate with and support other functions across the site as needed.
09Contribute to the smooth and efficient running of daily manufacturing operations.
10Maintain accurate and complete documentation throughout all manufacturing activities.
Exigences
↳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.
Avantages
