Position: Associate

Job type: Full-time

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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.

Reporting to the Franchise Quality Manager/Supervisor, the QA Project Team Lead will support planning and execution of assigned DePuy Synthes projects, utilizing robust project management and quality risk analysis in support of ongoing business needs. The QA Project Team Lead will serve as the project Quality representative for their franchise.

Main Responsibilities
  • Maintain Quality oversight and responsibility for assigned projects, ensuring there are no negative effects on the business and that they are executed compliantly.
  • Lead development of project Quality Plan and related quality deliverables, including solicitation of input from stakeholders and reviewers.
  • Ownership of development and maintenance of project change order management processes and supporting documentation.
  • Manage the activities of a defined team of QA personnel.
  • Management responsibilities include day-to-day work allocation and prioritization, performance and output quality review, coaching, training, internal communications, and general personnel assistance during the course of their duties.
  • Actively support all project goals and objectives.
  • Lead assigned project QA activity as defined and resolve problems & eliminate constraints to ensure project targets are met.
  • Represent the Quality function as required by management.
  • Ensure that all Health, Safety and Environmental requirements are fulfilled.
Who We Are Looking For
  • A degree level or similar qualification in mechanical or industrial engineering.
  • Minimum 3 years of experience in medical device manufacturing in a people management role.
  • English fluent
  • Demonstrated ability to successfully manage QA systems in the medical device industry.
  • Demonstrated knowledge and ability regarding product verification and process validations.
  • Demonstrated knowledge of medical device FDA, MDD and MDR GMP requirements.
  • Demonstrated experience in medical device regulatory distribution controls.
This role based in Le Locle (NE), Switzerland will initially be limited until 31.12.2022. If you are interested in working for a global leading health care company in a challenging role, then send us your application in English today. Or give us a call if you have any questions!
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Deadline: 04-05-2024

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