SENIOR PROCESS ENGINEER

Johnson & Johnson is recruiting for a Senior Process Engineer within the Manufacturing Science and Technology (MSAT) team located in Geel, 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 https://www.
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For more than 130 years, diversity, equity & inclusion (DEI) has been a part of our cultural fabric at Johnson & Johnson and woven into how we do business every day.
Rooted in Our Credo, the values of DEI fuel our pursuit to create a healthier, more equitable world.
Our diverse workforce and culture of belonging accelerate innovation to solve the world’s most pressing healthcare challenges.
Our expertise in Innovative Medicine is informed and inspired by patients, whose insights fuel our science-based advancements.
Visionaries like you work on teams that save lives by developing the medicines of tomorrow.
Join us in developing treatments, finding cures, and pioneering the path from lab to life while championing patients every step of the way.
Learn more at https://www.
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om/innovative-medicine The chemical production facility in Geel is part of the Johnson & Johnson Innovative Medicines Supply Chain organization and is the largest manufacturer of active pharmaceutical ingredients (APIs) and spray dried powders (SDP) within the network and our API Launch and Grow site.
The APIs/SDPs we manufacture are sent for further processing through pharmaceutical production into tablets, ointments, syrups, and other formulations, which are distributed to our patients around the globe.
The Senior Process Engineer will become a member of the MSAT Small Molecule Drug Substance Value Optimizer (SM DS VO) team who are responsible for supporting the ongoing production of our commercial Life Cycle Management (LCM) API portfolio.
They will represent MSAT as part of site-based multi-functional teams, and within global project teams throughout the business, collaborating closely with partners to guarantee smooth and efficient API production whilst ensuring that safety, environmentally sound practices, and quality are embedded in everything we do.
The primary focus of this role will be ensuring API manufacturing readiness, identifying and implementing process optimizations, leading non-conformance investigations / Corrective Actions Preventative Actions (CAPA) implementation, supporting process validation and qualification activities, and coordinating technology transfers.
The (Senior) Process engineer will also play a leading role in increasing agility and capacity at the Geel site through the application of scientific- and data-driven API manufacturing process improvements and will be recognized as the MSAT site expert for their API syntheses.
Key Responsibilities.
Partnering with the Operations, Quality, and Planning departments for daily operational support of API drug substance synthesis (e.
.
campaign preparation, resolution of non-conformances, CAPA implementation, process optimizations, production follow up, etc.) Leading complex process investigations or product related technical issues Identifying and implementing Cost Improvement Projects (CIP) (e.
., yield improvements, cycle time reduction, de-bottlenecking, etc.) and process optimizations.
Applying approaches such as process modelling / digital twins, advanced data-driven methodologies (e.
., multivariate analysis, data analytics, AI/ML technology etc.), and process analytical technologies (e.
.
infrared spectroscopy, focused beam reflectance measurement) to facilitate improved process understanding, optimizations, and non-conformance investigations.
Building process technology expertise and supporting the evaluation and introduction of new process technologies.
Collaborating closely with the global technology, data, and development functions to design specific technology solutions for optimized syntheses.
Leading/supporting slow moving and obsolete inventory (SLOB) avoidance activities.
Leading internal technology transfers and supporting external technology transfers.
Monitoring process and product performance (Continuous Process Verification, Product Quality Reviews).
Contribution, review, and approval of technical documentation Technical support in partnership with Quality in regulatory audits and inspections Qualifications Master’s Degree or PhD preferably in Chemical engineering or Process technology (bioengineering, industrial engineering or chemistry), or proven record in an industrial, operational environment.
At least 4 – 6 years of proven experience in chemical synthesis/API synthesis and/or process technology.
Experience in an API manufacturing or development environment is an asset.
Experience or knowledge in one or more of the following areas related to API manufacturing is preferred.
organic chemistry, reaction engineering, distillation, liquid-liquid extraction, solid-liquid separation, drying Knowledge or strong interest in one or more of the following areas is an asset.
process modelling, process analytical technology (PAT), data analytics, multivariate analysis, AI/ML, lean manufacturing (certification is a plus), process excellence (certification is a plus).
Awareness of API manufacturing site systems and procedures (SAP, complaint handling, change control, qualification, process validation, etc.) Good project management, planning, and coordination skills.
Motivated, able to work independently and take decisions autonomously, with demonstrated problem solving skills and results driven personality.
Strong interpersonal skills, e.
., influencing and handling conflicting interests.
Strong analytical skills with a high level of accuracy.
Able to establish close collaborations with internal and external business partners Working knowledge of English (both verbally and written) and Dutch (or willing to develop proficiency in Dutch) We will ensure the space and opportunities to lead and grow and learn via various professional trainings and certifications, but also strong future perspectives for variate career path opportunities.
Moreover, you will become one with a competent, dedicated and purpose-infused team! Johnson & Johnson is an Affirmative Action and Equal Opportunity Employer.
All qualified applicants will receive consideration for employment without regard to race, colour, religion, sex, sexual orientation, gender identity, age, national origin, or protected veteran status and will not be discriminated against on the basis of disability.
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