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Johnson & Johnson

Makes prescription drugs and medical devices

Manager Centre of Expertise LVV facility

Process EngineeringPosted on Nov 9
Full-timeSassenheim, Netherlands€76k - €121.4k /yrIn-person

About the Job

Requirements

  • A bachelor's or university degree, preferably in engineering, science, or a technical subject such as mechanical, electrical, automation, or process engineering, or equivalent.
  • Six to eight years of relevant experience as a people leader (supervisor and/or manager), leading and directing teams and/or departments.
  • More than 10 years of experience in a pharmaceutical Good Manufacturing Practice (GMP) production environment.
  • Tangible experience successfully implementing Lean projects, both in content and leadership.
  • Fluency in English.
  • Knowledge of Environment, Health, Safety and Sustainability (EHSS) standards and regulatory requirements in relation to LVV production.
  • Knowledge of the production process and GMP requirements.

Responsibilities

  • Provide leadership and direction for manufacturing specialist resources and activities.
  • Partner with Operations in the LVV facility to identify, define, and execute base business improvements.
  • Deliver technical requirements for equipment, single-use items, and continuous improvements.
  • Encourage and support the identification and development of innovative solutions to problems and opportunities.
  • Oversee technical changes and the execution of small- to medium-complexity equipment and disposable improvement projects.
  • Provide comprehensive technical advice.
  • Facilitate resolution of complex process and technical problems.
  • Promote innovation initiatives for new processes, products, and ideas.
  • Review and approve technical documentation to verify compliance with technical specifications and standards.
  • Communicate with internal and external partners, including Operations, Quality Assurance, Quality Control, MAM, MSAT, and Information Technology, to coordinate and execute project plans.
  • Assign tasks based on projected scopes, including compliance and quality improvement, cost reduction, cycle time reduction, capacity increase, raw material qualification, and launch preparation.
  • Support implementation of multiple new product development plans and programs for the business unit.
  • Monitor execution of plans and programs at lower levels and across functions.
  • Monitor correct execution of equipment maintenance and repair reports.
  • Collaborate with the maintenance department to evaluate recurring issues that may require equipment replacement.
  • Allocate resources to achieve goals within established timelines and budgets.
  • Ensure departmental and company compliance with local government and company regulations, policies, and procedures for health, safety, and environmental compliance.
  • Take rotating beeper duty.

About the Company

Johnson & Johnson

Makes prescription drugs and medical devices

Johnson & Johnson develops prescription medicines and makes medical devices for hospitals, and unlike most big drugmakers, it runs both businesses under one roof. In 2015, its Darzalex became the first antibody drug approved for multiple myeloma, a blood cancer. Its medicines treat cancer, immune diseases such as psoriasis, and mental illnesses such as depression, and patented drugs bring in most of its sales. Its MedTech unit makes heart pumps, catheters that treat irregular heartbeats, surgical sutures, and Acuvue contact lenses. It was founded in 1886 to make sterile surgical dressings, is based in New Brunswick, New Jersey, and spun off its consumer brands, such as Tylenol and Band-Aid, as Kenvue in 2023.

Company size
10,001+
Company stage
IPO
Headquarters
New Brunswick, NJ
Founded
1886

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