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Johnson & Johnson Loopbaan

Scientist Technical Operations

Leiden, Nederland


Requisition ID: 1805687698W

Leiden site Technical Operations (TO) is part of the global Technical Operations organization. TO manages the technology platform strategy within Leiden as well as across the other parenteral sites.  The strategy is locally executed by TO.

TO is responsible for validation and standardization of processes and equipment within the Janssen Biologics site and manages Life Cycle Management (LCM) projects and improvement projects. We accomplish this through our broad technical competency, global reach and local execution power. A job within the TO team is very dynamic and diverse. We are looking for someone who likes challenges, is collaborative and is keen on working within local as well as global project teams. And is capable to lead these teams.  

General responsibilities:

As Scientist you are the primary interface between the Leiden site Operations, Quality, BioTD departments and the TO organization. You ensure integration of the global standards into local production process and/or LCM projects or local improvement projects. In support of the global TO organization you are Subject Matter Expert for one of the commercial cell lines.

Specific tasks:
  • Management of LCM projects
  • Management of standardization projects
  • SME for one of the commercial cell lines, probably Simponi
  • Coordinator of resin lifetime studies, cleaning as well as process performance
  • Support of complex investigations, facilitation of risk assessments
  • Execution of (process) validation assessments, including reporting
  • Subject matter expert during internal and external audits and inspections
  • Manager and initiator of process improvements to remain competitive. Preparing business cases.
  • Leading technical JJPS initiatives
  • Networker, change agent to implement and validate new technologies

  • Master degree or in Science (Biomedical, Biochemical, Chemical Technology, Biotechnology, Pharmacy, Engineering)
  • Minimal 5 years of relevant work experience in the (bio-) pharmaceutical industry.
  • Good knowledge of EHSS and GMP requirements, high quality norm
  • Good large molecule API Process and process validation knowledge
  • Strong  Analytical, expertise in leading investigations
  • Influencing skills, excellent stakeholder management within a high complex matrix parenteral organization
  • Customer focused and Innovative
  • Excellent verbal as well as writing communication skills in English and Dutch.
  • Result oriented and organizational skills
  • Certified as FPX project lead and/or as Green or Black Belt is a plus
  • Modelling experience is a plus

Primaire locatie
Nederland-Zuid Holland-Leiden
Janssen Biologics (7266)
Requisition ID