Johnson & Johnson Carrières

Senior Process Engineer

Neuchâtel, Neuchâtel
Process Engineering

Description du poste

Requisition ID: 1805646863W

The Johnson and Johnson Family of companies is comprised of more than 250 operating companies in 57 countries employing approximately 128,000 people. Johnson and Johnson is the world‘s most comprehensive and broadly based manufacturer of health care products, as well as a provider of related products for the consumer, pharmaceutical and medical devices & diagnostics markets. At least a billion people around the world are touched each day by what we do.

DePuy Mitek, one of the legal manufacturer of the group Johnson & Johnson, develop, manufacture and distribute innovative medical products for sports medicine and for the reconstruction of muscles, ligaments and tendons is looking for a permanent contract:

Manufacturing Process Engineer (100%) – CDD 2 years – Neuchâtel

  • Serve as the process and equipment engineering to support manufacturing on a day to day basis
  • Provide engineering input to solve complex manufacturing process problems in the medical assembly environment, including a continuous focus on plant equipment and manufacturing processes to achieve cost and cycle time savings
  • Follow process performance metrics and initiate appropriate actions
  • Take the responsibility for the technical know-how of operators and technicians
  • Support closure of NRs, CAPAs, audit observations, ergonomics and safety related action items.
  • Lead Lean Manufacturing studies to improve assembly processes and to introduce new processes and equipment
  • Critically assess, improve and implement medical manufacturing processes to achieve cost reductions and quality improvements in line with agreed targets and priorities of Business Unit.
  • Create and execute validation strategies for medical device assembly processes and equipment, including writing validation protocols and reports (IQ, OQ, PQ), executing process tests, and analyzing the resulting data from validation activities
  • Ensure all Health, Safety and Environment requirements are met and new standards are implemented
  • Manage external equipment vendors through the process of machine design, procurement, and installation of new manufacturing equipment



·            Engineering Degree (automation/ mechanical / micromechanical background) from an accredited technical or manufacturing engineering program is required

·            Process Excellence Six Sigma and/or Lean certification is desirable

·            Experience in manufacturing and equipment engineering in the medical device industry will be appreciated

·            Project management experience to  support equipment development and introduce them into Manufacturing

·            Experience required in leading manufacturing process initiatives to achieve quality improvements and cost reductions

·            Thorough working knowledge of the validation requirements for Medical Devices with demonstrated experience; generate and execute equipment, process, and computer system validation.

·            Resistance to stress

·            Good organization skills and results oriented

·            Excellent communication skills; making complex issues easy for others to understand and the ability to prepare communications for team and project documentation. Ability to communicate across multiple levels in the organization

·            Fluent in French and English

Please note that we already have a pre-identified candidate for this position. however if you are interested in the role please don't hesitate to send your application.

Emplacement principal
Medos International Sarl (7898)
Process Engineering
Requisition ID