• Contract
  • Anywhere
  • Recruiter: Usha Rao

Reliability and Quality Engineer – 5915 URA

Our client, a dynamic global bio-pharmaceutical company headquartered in Switzerland, covering multiple therapeutic areas, is looking for a Reliability and Quality Engineer for a long term contract based in the Bern area.

Ideally this person will have close cooperation with all technicians, teams and departments. Helping to ensure that master data and new data match the life cycle data. Helping on any quality tasks like but not limited to:

  • CAPA documentation support
  • Non Conformance documentation support
  • Audit action support
  • Quality database support
  • Keep track on lead times and documentation quality.
  • Work in close collaboration with team leader on timeline & deliverables. Helping to update and shape internal written processes.

Main Responsibilities:

  • Remind individuals on their deliverables within the time frame of any quality actions.
  • Keep track of ongoing changes within the department
  • Support the team leader on quality actions
  • Working with engineers and equipment owners as well as external providers to be compliant with our processes
  • Internal exchange via technical drawing and document management systems to ensure that the requirements of the location are met.
  • Technical Optimization of processes and systems / improvement measures.
  • Creates impact assessments for quality tasks.
  • Initiates and identifies opportunities for technical and economical optimization of processes and systems.
  • Support the organization to guarantee the technical qualified status according to the current given internal and external requirements supporting the specific qualification owner

Qualifications and Experience:

  • Relevant working/residency permit or Swiss/EU-Citizenship required.
  • 8 to 10 years of experience in Project Engineering in Pharmaceutical industry.
  • Preferably engineering diploma (preferably mechanical, electrical, industrial, chemical) or equivalent experience.
  • Solid experienced in supporting GMP projects
  • User knowledge, experience in GMP quality systems
  • Aware of maintenance management, compliance, GMP and other regulatory standards
  • Excellent oral and written communication skills at different hierarchical levels.
  • Ability to work in a matrix organization.
  • Ability to lead without direct management responsibility.
  • Excellent analytical skills.
  • Team player, strong communication, innovative, knowledgeable