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Manufacturing Operations Specialist (m/f/d)

Lucerne Interim View Job Description
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.

added 13/02/2025

  • Prestigious pharmaceutical company
  • Temporary project for 1 year

About Our Client

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.

Job Description

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

  • Executes and troubleshoots manufacturing processes under GMP regulations
  • Ensures compliance with GMP and EHS standards
  • Documents process execution, deviations, and changes; collaborate with Quality Assurance
  • Supports process improvements and new technology implementation
  • Manages SOPs, batch records, and technical documentation
  • Handles material management using ERP systems (SAP)
  • Mentors junior team members and facilitate knowledge transfer
  • Participates in sampling activities and on-call duties, including weekend

The Successful Applicant

To 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
  • Willingness to work on weekends as required

What's on Offer

A challenging and rewarding position in a globally recognized company.

Contact
Christina Beer
Quote job ref
JN-012025-6646502

Job summary

Job Function
Engineering & Manufacturing
Specialisation
Quality
Industry
Healthcare / Pharmaceutical
Location
Lucerne
Contract Type
Interim
Consultant name
Christina Beer
Job Reference
JN-012025-6646502

PageGroup is an equal opportunity employer committed to workforce diversity, both as an employer as well as a recruitment service provider. Each recruitment decision we make for people we hire and people we place into new roles is based solely on the candidates’ knowledge, experience and skills.