Manufacturing Operations Specialist

vor 3 Wochen


Luzern, Schweiz K-Recruiting Life Sciences Vollzeit

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We unite the people who make our world healthier by placing top experts with life sciences companies worldwide. Fast and reliably, with the perfect…

Specialist Manufacturing Operations (M/F/D)

Tasks:

  • Set up, practical execution and troubleshooting of upstream, downstream and support unit operations in continuous manufacturing and fed-batch processes under Good Manufacturing Practices (GMP)
  • Knowledge of and compliance to GMP principles and EHS standards in the area of responsibility
  • Management and documentation of process execution, deviations, changes and CAPAs. Partnering with Quality Assurance and other internal stakeholders during investigations and technical discussions
  • Involvement in continuous improvement efforts and support for the implementation of new technologies, including non-GMP engineering runs or testing activities
  • Creation and updates of SOPs and (electronic) master batch records. Technical review of various documentation related to process transfer and GMP manufacturing
  • Participation in sampling activities or on-call duties, which may include weekend work

Qualification:

  • Educational background in a relevant discipline
  • A minimum of 2-5 years of work experience in the pharmaceutical or biotech industry
  • Experience (2-5 years) or educational background in upstream or downstream processing. General knowledge of unit operations in manufacturing processes for biologics and of GMP requirements
  • Ability to solve problems and take new perspectives on existing solutions with a desire to continuously learn, improve and develop. Ability to perform under pressure in a complex GMP environment.
  • Business Fluent in English and German: Effective oral / written communication skills in English (C1) Oral / written communication skills in German (B1)

Preferred Experience and Skills:

  • A bachelor’s or master’s degree in a relevant discipline
  • Experience with quality management and compliance systems (Trackwise/SAP QM/VeevaVault)
  • Familiarity with the use of automated systems in manufacturing (DeltaV) or electronic batch records (MES)
  • Prior experience with process development or process scale-up is beneficial
  • Ability to work efficiently as part of a team, as well as willingness to take responsibility for independent projects

Requirements:

Start: asap

Duration: 31.12.2026

Seniority level
  • Associate
Employment type
  • Full-time
Job function
  • Manufacturing
  • Industries
  • Pharmaceutical Manufacturing
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