GMP Production Engineer

Vor 3 Tagen


Luzern, Luzern, Schweiz Randstad Vollzeit
Manufacturing Operations Role

We are seeking an experienced Process Engineer - II - P2 Specialist, Manufacturing Operations to join our team. In this role, you will be responsible for supporting GMP manufacturing activities and ensuring seamless integration within the existing team.

About the Position
  • Establish and maintain effective relationships with Quality Assurance and other internal stakeholders to ensure smooth process execution.
  • Develop and implement process improvements to enhance efficiency and productivity.
  • Manage documentation for process execution, deviations, changes, and CAPAs while collaborating with internal stakeholders.
  • Support the implementation of new technologies, including non-GMP engineering runs or testing activities.
  • Develop and maintain SOPs and electronic master batch records, as well as review technical documentation for process transfer and GMP manufacturing.
  • Manage material using ERP systems (e.g., SAP).
  • Train and mentor junior team members and actively participate in knowledge transfer.
  • Participate in sampling activities or be on-call, including potential weekend duties.
Requirements
  • Educational background in a relevant discipline.
  • 2-5 years of experience in the pharmaceutical or biotech industry.
  • Minimum of 2 years of practical experience in the GMP manufacturing of biologics (upstream or downstream).
  • Expert knowledge in specific unit operations for biologics manufacturing.
  • Understanding of GMP principles and ability to work under pressure in a complex environment.
  • Fluent English communication skills (C1 level).
  • Intermediate German skills (B2 level). Candidates with German A1/B1 proficiency may be considered if other skills strongly align with the role.


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