Manufacturing Operations Specialist (m/f/d)

Job title:

Manufacturing Operations Specialist (m/f/d)

Company

Michael Page

Job description

The selected candidate will be responsible for the following task area:

  • Responsible for setting up, operating, and troubleshooting upstream and downstream processes in continuous and fed-batch manufacturing under GMP guidelines.
  • Ensures adherence to GMP and EHS standards by accurately documenting processes, managing deviations, changes, and CAPAs, and collaborating with Quality Assurance and other stakeholders.
  • Drives process optimization initiatives and supports the integration of new technologies through non-GMP engineering runs and testing activities.
  • Prepares and maintains SOPs and electronic master batch records while performing technical reviews of GMP documentation.
  • Manages materials using ERP systems such as SAP to ensure an efficient workflow.
  • Participates in sampling activities and is available for on-call duties, which may include occasional weekend work.

Prestigious pharmaceutical companyTemporary project for the next 2 yearsTo be considered for this position, the ideal candidate must have:

  • Successfully academic degree in a related field.
  • At least 1-3 years of working experience in the pharmaceutical or biotech industry, with experience in GMP biologics manufacturing (upstream or downstream processing).
  • Hands-on experience with quality management systems such as Trackwise, SAP QM, or VeevaVault.
  • Familiarity with DeltaV and electronic batch record systems (MES).
  • Excellent command of English (both written and oral), good German skills (level B1) are required
  • Prior involvement in process scale-up or technology transfer.
  • A proactive, reliable, and independent approach to work.

Our client, a global leader in the pharmaceutical industry, is seeking a motivated Specialist to join their Manufacturing Operations team in the greater Lucerne area. This full-time, on-site role offers an exciting opportunity to contribute to the implementation and GMP manufacturing of early-phase clinical therapies in a collaborative and forward-thinking environment.A challenging and rewarding position in a globally recognized company.

Expected salary

Location

Lucerne

Job date

Thu, 23 Jan 2025 23:06:28 GMT

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