Job type: Full-time

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Job content

Our client is a fast growing medical device company.

Responsibilities :
  • Manage Engineering activities and collaborate closely with Supply Chain and Manufacturing meetings;
  • Lead cross functional teams and suppliers to ensure targets are reached with good resources and budget;
  • Set up plans in place to meet the business needs with additional capital expenditure as required;
  • Drive safety, quality, delivery targets and ensure expectations are understood by all teams;
  • Support and encourage continuous improvement activities across the site;
  • Conduct all duties in compliance with Good Manufacturing Practice (GMP), Good Documentation Practice (GDP) and appropriate regulatory requirements;
  • Bring and deploy action plans to improve internal processes and act as solutions driven director with an innovative mindset;
  • Proactively ensure all equipment is support by effective maintenance plans, clearly defined and administered in line with business needs to ensure all commitments are achieved;
  • Develop a detailed product and process knowledge to realize synergies and opportunities between all business.
Profile :
  • Mechanical or Electromechanical Degree with experience of application in Biotech or Medtech business;
  • Justify more than 5 years of experience in a leadership position during a time of change and growth;
  • Large experience of managing engineering and facility activities in a regulated environment;
  • Extensive knowledge of FDA and ISO 13485 manufacturing process;
  • Facilities management covering HVAC monitoring is a good plus;
  • Fluent in English and French.
Permanent contract #boost
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Deadline: 09-06-2024

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