Job Information
J&J Family of Companies Experienced Engineer – Manufacturing Sciences and Technology in Beerse, Belgium
At Johnson & Johnson, we believe health is everything. Our strength in healthcare innovation empowers us to build a world where complex diseases are prevented, treated, and cured, where treatments are smarter and less invasive, and solutions are personal. Through our expertise in Innovative Medicine and MedTech, we are uniquely positioned to innovate across the full spectrum of healthcare solutions today to deliver the breakthroughs of tomorrow, and profoundly impact health for humanity. Learn more at jnj.com (https://www.jnj.com.) .
As guided by Our Credo, Johnson & Johnson is responsible to our employees who work with us throughout the world. We provide an inclusive work environment where each person is considered as an individual. At Johnson & Johnson, we respect the diversity and dignity of our employees and recognize their merit.
Job Function:
Supply Chain Engineering
Job Sub Function:
Process Engineering
Job Category:
Scientific/Technology
All Job Posting Locations:
Beerse, Antwerp, Belgium
Job Description:
Position: Experienced 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 PPDS we are looking for a Manufacturing Sciences & Technology Experienced Engineer in the Pharmaceutical Supply & Engineering Sciences (PSES) organisation, located in Beerse, Belgium. You will be accountable for the management and execution of early development clinical manufacturing activities for synthetic-molecule drug products with a primary focus on the internal Drug Product Pilot Plant (DP-Pilot Plant). This role covers processes for oral solids, liquids, and especially parenteral applications, across small-scale and pilot-scale operations and the use of innovative pilot-plant manufacturing platforms.
Your Role
As a Manufacturing Sciences & Technology (MST) Experienced Engineer you will be a core member of the Pharmaceutical Supply and Engineering Sciences organization, focused on early development in the internal pilot plant.
The MST engineer is responsible for successful introduction and follow-up of clinical manufacturing activities in the Drug Product (DP)-Pilot Plant (PP), being the PSES representative in the drug product development teams.
Working within an international setting and in crossfunctional teams, the MST engineer is responsible for and supports:
Lean and right first-time process introduction during early development in the internal pilot plant,
Pilot-plant manufacturing readiness,
Potential scale-up & tech-transfer preparation of drug product processes from the PP to commercial manufacturing facilities from a (clinical) manufacturing perspective.
Technologies span over processes for oral solids, liquids and parenteral applications, ranging from small scale to pilot-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:
- Potential scale-up & tech-transfer preparation of drug product processes from the PP to commercial manufacturing facilities from a (clinical) manufacturing perspective.
· 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 internal point of contact within development and pilot-plant operations 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.
- Potential scale-up & tech-transfer preparation of drug product processes from the PP to commercial manufacturing facilities from a (clinical) manufacturing perspective.
· Drive the evolution of existing workflows by addressing challenges head-on and uncovering opportunities to enhance early development pilot-plant 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 and pilot-plant teams.
- Potential scale-up & tech-transfer preparation of drug product processes from the PP to commercial manufacturing facilities from a (clinical) manufacturing perspective.
· 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 pilot plant, acting as a key collaborator and partner for the DP development team, contributing to advancements in pharmaceutical manufacturing and assuring right-first-time manufacturing 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.
Strong/basic to profound knowledge of parenteral manufacturing activities (e.g., sterile handling, aseptic filling, vial/syringe workflows) is a key advantage. 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 (focus on internal cross-functional partners and pilot-plant teams).
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 5% 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.
Required Skills:
Preferred Skills:
Analytical Reasoning, Computerized Equipment Skills, Emerging Technologies, Gemba Kaizen, Issue Escalation, Lean Supply Chain Management, Problem Solving, Process Control, Process Engineering, Process Oriented, Product Improvements, Science, Technology, Engineering, and Math (STEM) Application, Situational Awareness, Supply Planning, Technical Research, Technologically Savvy, Validation Testing