Laboratory Quality Engineer / Johnson&Johnson

☞ Randstad Switzerland

View: 124

Update day: 24-04-2024

Location: Neuchâtel Neuchâtel NE

Category: Quality Assurance / Quality Control

Industry: Staffing Recruiting Biotechnology Research Pharmaceutical Manufacturing

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.

The Laboratory Quality Engineer applies intermediate Quality Engineering/Scientific Method techniques and principles to daily tasks and activities as well as managing project dedicated to laboratory. In addition, applies relevant regulations, standards, and industry best practices to assignments. Plans and conducts projects and assignments with technical responsibility or strategic input. Receives intermittent, moderately detailed instructions from technical Quality leaders at various levels, in addition to other stakeholders.

Responsibilities
  • Utilize quality engineering principles and problem-solving skills to manage project for products/processes/laboratory.
  • Collaborate with project teams and business partners to ensure compliance. with company policies and procedures as well as medical device regulations.
  • Develop, Plan, execute and report project activities.
  • Manage validation of test equipment and/or test methods.
  • Establishes maintenance and calibration schedule for test equipment based on manufacturers recommendations and maintains equipment records.
  • Ensure that Test Methods and Quality procedures are executed in compliance with specifications and standards.
  • Work in development, writing, updating and review of test methods, SOPs, protocols and specifications as required.
  • Change control management for documents.
  • Support Base Business and Production Initiatives.
  • Responsible for communicating business related issues or opportunities to next management level.
  • Investigates Out of Specification / Out of Trend data, including raising the appropriate Quality System records and performing associated corrective actions.
  • Complies with site HSE and quality procedures.
  • Responsible for ensuring personal and Company compliance with all Federal, State, local and Company regulations, policies, and procedure.
  • Performs other duties assigned as needed.
Who We Are Looking For
  • University/Bachelor’s Degree or Equivalent in Engineering or Science.
  • Quality background with up to 2 to 3 years in industry, preferred in medical field
  • Laboratory Background with expertise in lab testing, developing and validating test methods, and equipment management in a regulated Quality Lab
  • Project management background
  • Process Validation expertise is preferred
  • Quality and Statistical tools knowledge.
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: 08-06-2024

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