Manufacturing Engineer II

Bio-Rad Laboratories AG

Cressier FR
Postuler
  • Date de publication:

    20 juin 2022
  • Taux d'activité:

    100%
  • Type de contrat:

    Durée indéterminée

Manufacturing Engineer II

Manufacturing Engineer II

ID der Stelle


2022-28999



# der offenen Position


1



Ort


CH-FR-Cressier



Kategorie


Ingenieurwesen

Überblick

Bio-Rad is a global leader providing a broad array of clinical diagnostics and life science research products. With a team of more than 8,000 employees and a global network of operations serving our customers, we help people live longer, healthier lives.

Bio-Rad was founded over six decades ago and has continued to provide the healthcare industry with innovative and useful products that help life science researchers accelerate the discovery process and medical diagnostic labs obtain faster, better results.

 

Based in its Cressier site, Bio-Rad is looking for a Manufacturing Engineer (100% - M/F).

Verantwortlichkeiten

Project management and continuous improvement:


  • Drive project management from A-Z (budget, planning, resources and communication) for manufacturing at the Cressier facility

  • Coordinate the Manufacturing Project Portfolio

 

Engineering:


  • Automation and continuous improvement (equipment, processes, cleaning, steriliztation, utilities)

  • Lead investigations, root cause analysis, corrective and preventive actions and closure of exception management documentation in a timely manner

  • Participate in the development of the qualification/validation activities (URS, SAT, FAT, IQ, OQ, PQ), including review of design and engineering specifications and ensure the interface for new process/equipment/product within manufacturing operation

  • Work with external companies to drive specific development and automation programs

  • Develop and implement appropriate tools and methods to perform standard investigation and problem-solving techniques, to close exception documents and to ensure appropriate adherence to quality documents

  • Assist and participate in performing complaint investigation and in CAPA process investigation, as needed

Qualifikationen


  • Min. 5 years of experience in project management (with certification) and engineering, ideally in a diagnostic/pharmaceutical environment

  • Good interpersonal (coach), problem solving, moderation and negotiation skills

  • Open minded flexible, tolerant, pragmatic, analytic and resilient

  • Good understanding of cGMP requirements

  • Native French or German with good knowledge of the other language and good English skills (speaking and writing)

  • Business and customer oriented - innovative and creative

  • Expertise in continuous improvement, ideally Green Belt certification

Optionen

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