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Position: Scientific Senior Engineer – Manufacturing Sciences and Technology

About the Department

Join the Global Pharmaceutical Product Development and Supply (PPDS) organization within the Therapeutics Development and Supply (TDS) team at Johnson & Johnson. Based in Beerse, Antwerp, Belgium, our development centers span the US, Asia, and Europe, driving the creation of cutting-edge pharmaceutical dosage forms.

Within the PPDS department we are looking for a Manufacturing Sciences & Technology Scientific Senior Engineer in the Pharmaceutical Supply & Engineering Sciences (PSES) organisation, located in Beerse, Belgium. You will be accountable for the management of clinical manufacturing of synthetic molecule drug products across our network with a focus on the internal drug product pilot plant. This role will encompass processes for oral solids, liquids, and parenteral applications, covering both small-scale and large-scale operations, as well as the utilization of innovative manufacturing platforms.

Your Role

As a Manufacturing Sciences & Technology (MST) Engineer you will be a key player in our Pharmaceutical Supply and Engineering Sciences Organization.

The MST engineer is responsible for successful introduction and follow-up of clinical manufacturing activities in the Drug Product (DP)-Pilot Plant (PP) and at external manufacturers as External Supply Integrator (ESI), being the PSES representative in the drug product development teams.

Working within an international setting and in crossfuctional teams, the MST engineer supports

• Lean and right first-time process introduction from (early) contract development and manufacturing organization (CDMO) sites,
• Manufacturing Plant readiness,
• Potential scale-up & tech-transfer of drug product processes from the PP to commercial manufacturing facilites from a (clinical) manufacturing perspective.

Technologies span over processes for oral solids, liquids and parenteral applications, ranging from small scale to large scale processes e.g. from a single punch tablet press to a continuous manufacturing line and e.g. syringe and vial filling lines for parenteral production.

As a key player of our PSES team, you will help shape the future of drug product formulation and process development. Your responsibilities will include:

• Dynamic Project Leadership and Coordination
  • Act as PSES representative in Drug Product Development and Clinical Supply Chain project teams, assuring and coordinating DP clinical readiness activities.
  • Serve as the primary point of contact towards early development CDMOs and team members, fostering collaborative relationships to internalize new manufacturing processes that ensure right-first-time outcomes while optimizing workflows.
  • Proactively identify, lead, and navigate project critical path milestones, adeptly managing risks and implementing innovative corrective actions to sustain robust process development and successful clinical manufacturing.
• Transformative Process Improvement and Optimization
  • Drive the evolution of existing workflows by addressing challenges head-on and uncovering opportunities to enhance (early) development tech transfers, manufacturing, and business processes within an international team and on a global scale.
  • Establish, review, and endorse manufacturing instructions and specifications, collaborating effectively with internal departments as well as early development manufacturing sites and global CDMO representatives.
• Innovation-Focused Expertise - Development and Collaboration for Success

• Cultivate manufacturing sciences expertise across diverse manufacturing platforms through cross-functional collaboration with development teams and subject matter experts, ensuring alignment with latest industry standards.
• Take ownership of the successful introduction of clinical manufacturing activities in the internal or external manufacturing site, acting as a key collaborator and partner for the DP development team, contributing to advancements in pharmaceutical manufacturing and assuring right first time manfuacutring of clinical drug product material.

Your Qualifications

• MSc or PhD in chemistry, pharmaceutical sciences, (bio)chemical or mechanical engineering, or other discipline within pharmaceutical/biotechnology sciences with at least 2 years experience in GMP regulated pharmaceutical development/engineering area.
• Familiarity with oral solid dosage, liquid, and/or parenteral products, as well as conventional and some innovative manufacturing technologies like spray drying, extrusion, and continuous manufacturing. Basic understanding of process analytical technologies is desirable.
• Experience working in regulated environments (e.g., FDA standards and general GMP guidelines) is important. Awareness of relevant internal and external regulations regarding equipment requirements and processes through literature, workshops, and training is beneficial.
• Good organizational and coordination skills, with knowledge of risk management. Able to search literature and utilize other resources effectively to apply and advance knowledge practically.
• Good collaboration and influencing skills to partner effectively at different levels and across multiple groups. Able to establish working relationships with internal teams and external partners. Experience managing projects within the Asian Region is a helpful asset.
• Technical expertise is valued, alongside developing project management skills. A willingness to explore advanced data sciences and related tools is a plus.
• Understanding of qualification, validation, and change management systems in the pharmaceutical industry is an advantage.
• Proactive and strong communication skills are essential for working in a global and dynamic setting. Ability to work independently under challenging timelines while maintaining a focus on quality is important.
• Fluency in English, both written and spoken, is required. Proficiency in Dutch is a helpful additional skill.
• Willingness to travel up to 10% of the time.

Our Offer

• Exciting Opportunities: Join an international and dynamic environment that promotes continuous learning and personal growth.
• Prime Location: Work at a site that encompasses all aspects of drug discovery and development, just a stone’s throw from the vibrant city of Antwerp.
• Competitive Benefits: Enjoy a competitive salary, on-site sports facilities, health programs, and family benefits that support your well-being.
• Inclusive Culture: Be part of a diverse team where your opinions are valued, and a healthy work-life balance is a priority.

If you’re ready to take the next step in your career and make a meaningful impact, we want to hear from you!

We will ensure that individuals with disabilities are provided with reasonable accommodation to participate in the job application or interview process, to perform essential job functions, and to receive other benefits and privileges of employment. Please contact us to request accommodation.

Johnson & Johnson is an Affirmative Action and Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, age, national origin, or protected veteran status and will not be discriminated against on the basis of disability.