Job Detail

• Job TitleProcess Engineering Pharma


• Vacancy Reference Number12921


• Work SiteSwitzerland / | CHE - All Regions / Basel


• Contract TypePermanent [Full-Time]


• Minimum number of years of experience required5 years of experience and more

Our offer

• A permanent contract with the leader in innovation and high-tech engineering consulting


• A multi-stage model with career opportunities through specialization prospects, as well as with over 45'000 consultants around the world and revenue of EUR. 2.9 Bn, the Altran Group is the undisputed global leader in Engineering and R&D services (ER&D).


• In Switzerland, Altran employs more than 250 consultants and aims towards large growth with offices located in Zürich, Basel, Lausanne and Geneva.


• Altran deploys its expertise particularly in:
  
  
  
  • Life Sciences (Pharma, Biotech, and Medical Devices),
  
  
  • Industry, Aerospace, Automotive, Energy, Railways,
  
  

Your role

• Assess existing processes and equipment and identify and implement improvements.


• Implement new or transferred manufacturing processes in a timely manner.


• Lead and/or participate in equipment and process validations, assist in troubleshooting of process and/or equipment issues.


• Automation & Factory Support specifics:
  
  
  
  • Assist in designing and implementing new equipment and tools to improve manufacturing efficiencies, reduce ergonomic stress, and improve quality.
  
  
  • Create and update drawings using Pro/Engineer or SolidWorks.
  
  
  • Work as part of a project team in the development and/or implementation of new equipment and tools.
  
  
  • Technical support for daily production issues related to manufacturing equipment.
  
  


• Assist in addressing, owning, and resolving quality related issues for the manufacturing departments (ex CAPAs, and Audits)

Your profile

• Master degree in a directly related discipline (Engineering, Biology, etc).


• Minimum 5 years of related experience Knowledge,


• Automation & Factory Support specifics:
  
  
  
  • Experience with automated manufacturing equipment and automation technologies.
  
  
  • Experience with Lean Systems.
  
  


• Quality Support specifics:
  
  
  
  • Experience in reagent or instrument manufacturing for a Medical Device or Pharmaceutical company.
  
  
  • Experience in a regulated environment. Knowledge of FDA Quality System Regulations (QSRs).
  
  


• Languages: English fluent, German is a plus