Overview
Process Operator role in microparticle manufacturing within a GMP-compliant setting. You will execute and oversee manufacturing processes, aim for operational excellence, support audits, and collaborate across teams to maintain high standards of quality, safety, and efficiency.
Responsibilities
* Operate and monitor production processes according to SOPs, GMP, and HSE standards.
* Document environmental and water monitoring activities.
* Review and archive batch records and production documentation.
* Identify and report process deviations and quality issues.
* Maintain cleanliness and order in production areas.
* Manage material flow: ordering, receiving, inventory, and disposal.
* Support internal and external audits.
* Troubleshoot technical issues in collaboration with engineering.
* Mentor junior staff or trainees when needed.
What You Bring
* Completed vocational training in a technical or pharmaceutical field.
* 3-5+ years of experience in pharmaceutical production.
* Strong knowledge of GMP and process safety.
* Proficiency in SAP and MS Office.
* Fluent in German (mandatory).
* A collaborative mindset and commitment to continuous improvement.
For further information, please apply with your CV.
Please note: Only candidates with the right to work in Switzerland can be considered (e.g., EU citizens or holders of a valid Swiss work permit).
Seniorities
* Seniority level: Entry level
Employment type
* Full-time
Job function
* Manufacturing
Industries
* Manufacturing
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