Position: Entry level

Job type: Full-time

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Job content

Caring for the world … one person at a time inspires and unites the people of Johnson & Johnson. This culture of caring is the focus of our corporate philosophy, that is anchored in the internationally applicable Credo. We embrace research and science - bringing innovative ideas, products and services to advance the health and well-being of people. Employees of the Johnson & Johnson Family of Companies work with partners in health care to touch the lives of over a billion people every day, throughout the world. We have more than 260 operating companies in more than 60 countries employing approximately 134,000 people. Our worldwide headquarters is in New Brunswick, New Jersey, USA.

ETHICON Neuchâtel is responsible for the production of implants for the treatment of female incontinence and bio-resorption products to stop bleeding during surgical procedures.

Responsibilities

Under supervision of the engineering manager and in accordance with all applicable federal, state and local laws/regulations and Corporate Johnson & Johnson, procedures and guidelines, this position:
  • Lead equipment design and validation project and process improvements projects.
  • Follow compliance and EHS policies and guidelines.
  • Work with vendors to procure new equipment and ensure new equipment and processes conform to all pertinent guidelines.
  • Responsible for performing and documenting activities for IQ, OQ and PQ.
  • Responsible for creating production documentation and providing input into new product BOMs, routings, and DMR.
  • Provide input into regulatory submissions i.e. PMA submission.
  • Technical writing, data analysis, data tracking and trending.
  • Support raw material and supplier qualifications.
  • Provide input into annual budgets and manage project spending.
  • Identify and lead opportunities to reduce cost of goods for future implementation.
  • Support closure of NCRs, CAPAS, audit observations, ergonomics and safety related action items.
  • Support critical engineering tasks in other departments as assigned.
  • Use project management tools and methodologies to deliver projects on-time, on-budget, and on-scope.
  • Serve as the engineering approver for process development studies and validation documentation when authorized.
  • Provides complex technical support for project planning, development, implementation, and modification; contributes extensively to engineering standards development balancing corporate and customer needs.
  • Performs complex research of new technology for potential corporate application.
  • Performs complex assignments designed to continue the development of professional work knowledge and abilities requiring advanced application of standard engineering techniques, procedures and criteria in carrying out engineering tasks.
  • Exercises independent judgment on significant details of work and makes selections and adaptations of engineering alternatives.
  • Performs assignments that have complex objectives and require the investigation of multiple variables.
  • Performs work which involves complex conventional types of plans, investigations, surveys, structures, or equipment with highly complex features for which there may be no precedents.
  • Assignments usually include several of the following: equipment design and development, test of materials, preparation of specifications, process study, research investigations, and report preparation.
  • Provides complex design reviews and feedback for improvements in manufacturability.
  • Develops equipment, materials, and process performance requirements, performs vendor searches and equipment evaluation to ensure adequate capability to produce quality products in required quantities at effective costs.
  • Designs experiments and capability studies, develops process specifications, and designs and procures process tooling.
  • Analyzes new processes and equipment the intent of achieving continuous improvement of present methods.
Who We Are Looking For
  • University / Bachelors Degree, Engineering degree or Equivalent
  • Mechanical and automation background with 1 to 3 years in industry, preferred in medical field
  • Equipment and Process Validation / Establish Equipment requirements (CAR request, URS,FAT)
  • Manufacturing processes improvements
  • Lean and/or Six Sigma belt
  • Automation and vision system optimization
  • Ability to work in a team environment
  • Ability to communicate across multiple levels in the organization
  • CAPA, NR, Audit (internal & External)
  • Machine safety
  • Good level in English
This role based in Neuchâtel, Switzerland will initially be limited to approx. 12 months. If you are interested in working for a global leading health care company in a challenging role, then send us your application in English or French today. Or give us a call if you have any questions!
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Deadline: 09-06-2024

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