Johnson & Johnson

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Originele vacaturetekst

Project Engineer

Job Description

Janssen Biologics in Leiden, the Netherlands, is a leading production site within Johnson & Johnson. At the Leiden site commercial pharmaceutical products & vaccines are being produced and new products are being developed.

Function Description:

As a Project Engineer you will be responsible for the acquisition and design of brand-new technology for our production plant. With the introduction of new technology, you will contribute to the critical delivery of products to patients and will have a direct impact on the future of the Leiden site!

In this role, you will coordinate all engineering disciplines and you will interact with internal and external stakeholders to bring conceptual ideas to final solutions. The Project Engineer is responsible for the quality, progress, and deliverables of the project within set budget and time frame. You will have to meet the pharmaceutical Safety, Health, GMP and Environmental standards to ensure safe and effective operation of the, by your team, designed equipment. To ensure proper alignment with the Johnson & Johnson network, you will work with a variety of subject matter experts from all over the world, broadening your experience.

The position is a very versatile and challenging position with, often, multiple challenges in parallel! The role goes way beyond the technical focus: You’ll have a high interaction with all aspects of the company, whether Operations, Labs, R&D or Quality, both local and within the Johnson & Johnson enterprise.

Most important Responsibilities & Accountabilities:

  • Act as Core Team Member in multidisciplinary project teams, representing all engineering disciplines and coordinate the complete engineering scope with other involved engineers.
  • Check and approve drawings and calculations for design or construction and verify that design is in-line with the Dutch, European and Janssen Biologics standards
  • Manage progress and quality with external engineering firms, on site contractors and internal stakeholders
  • Coordination of modifications with stakeholders and participate in Management of Change to ensure proper implementation
  • Coach and support team members and peers in applying and developing our engineering standards

Qualifications, Education, Skills & Experience:

  • Bachelor/Master degree in a technical or life sciences discipline
  • Minimum of 3 year working experience as engineer in a related field of work
  • Understanding of regulatory requirements and industry guidelines specific for the pharmaceutical industry and maintenance & engineering (GMP, CE, Machinery directive EU etc.)
  • Familiar with ISPE Guidelines and Standards is a plus
  • Experience with EHS, FMEA/HAZOP standards & assessments
  • Flexible, can deal with changing priorities
  • Natural motivator and team builder
  • Enthusiastic team player with a “Can do” attitude
  • Practical technical understanding, analytical and conceptual thinking
  • Excellent communication skills in writing, presenting, and speaking (English and preferably Dutch)
Primary Location
Netherlands-South Holland-Leiden-
Janssen Biologics (7266)
Job Function
Requisition ID
Type vacature:


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