Sr Principal Eng

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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.

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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; Latina, Italy

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 We are searching for the best talent for a Sr Principal Eng - Process Engineering to join our Team This is an onsite/hybrid role. Please note that this role is available across multiple countries and may be posted under different requisition numbers to align with local requirements.

While you are welcome to apply to any or all of the postings, we recommend focusing on the specific country(s) that align with your preferred location(s): Belgium & Italy – Requisition Number: R-071736; Puerto Rico – Requisition Number: R-076777; Switzerland – Requisition Number: R-076783. Remember, whether you apply to one or all of these requisition numbers, your applications will be considered as a single submission.

As the GET PE – Synthetics Drug Product Manufacturing Senior Principal Engineer, you will lead early design inputs and technical strategy for synthetic's drug product manufacturing processes within strategic capital projects, network studies, and technology platforms across IMSC.

You will provide deep technical expertise in the synthetic's controlled bioburden-drug product manufacturing (OSD and innovative forms such as semi-solid) and drug product intermediate through bioavailability enhanced technologies, while supporting solving and optimization activities at internal and external manufacturing sites. Joining our global engineering group, you will collaborate with high‑performing, multi‑functional teams across multiple sites and functions.

This role offers a dynamic and inspiring work environment with significant opportunities to influence technology direction, standardization, and capability building across the network.

• Lead the intake, scoping, prioritization, and resolution of syntheticscontrolled bioburden- drug product manufacturing related technical requests across global sites
• Lead and influence early‑phase process design and domain expertise for oral solid dose (OSD) products, covering both batch and continuous manufacturing platforms; as well new innovative drug product forms
• Lead and influence early‑phase process design and domain expertise for bioavailability enhanced technologies, including amorphous solid dispersions (ASD) with a strong emphasis on spray drying, as well as other technologies such as Self-Emulsifying Drug Delivery Systems (SEDDS) and other related innovative drug product intermediate formulation approaches
• Ensure robust, fit‑for‑purpose process design while promoting standardization and platform approaches where they make valuable contributions
• Provide expert input and alignment on key process, equipment, and technology selection decisions for drug product manufacturing
• Actively collaborate with other functions such as R&D, MSAT, Quality, EHS and Operations leads across synthetic drug product sites
• Find opportunities for harmonization, shared solutions, and best‑practice exchange across the network
• Foster a culture of collaboration to reduce duplication, accelerate implementation, and improve speed‑to‑market
• Maintain strong connections with industry experts and external networks (e