We are recruiting for a motivated professional MSAT Process Engineer to join a leading CDMO and pharmaceutical manufacturer based near Basel for an initial 6‑month contract with a chance to be extended for further. In this role you will be responsible for oversight of maintenance plans within the GMP manufacturing area.
Responsibilities
* Develop and maintain Standard Operating Procedures (SOPs):
o Analyse existing processes for optimization.
o Document procedures in line with internal guidelines and regulatory standards.
o Collaborate with specialist departments such as Production, Quality, and Technology.
* Plan and manage maintenance activities:
o Create and update maintenance plans for systems and operating resources.
o Coordinate scheduled maintenance measures to ensure operational efficiency.
o Prepare technical documents, reports, and protocols.
o Maintain compliance with documentation standards and ensure traceability.
o Organize filing and version control within digital systems.
Requirements
* Proven experience in technical documentation or maintenance.
* Familiarity with GMP‑regulated environments (advantageous).
* Proficient in MS Office; SAP knowledge is a plus.
* Highly structured and able to work independently.
* Strong written and spoken German; English skills are an advantage.
Seniority level
Not Applicable
Employment type
Contract
Job function
Biotechnology Research and Pharmaceutical Manufacturing
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