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Principal Engineer DAP TLI

Job in 6300, Zug, Kanton Zug, Switzerland
Listing for: Johnson & Johnson Innovative Medicine
Full Time position
Listed on 2026-10-12
Job specializations:
  • Engineering
    Packaging Engineer, Quality Engineering, Validation Engineer, Manufacturing Engineer
Salary/Wage Range or Industry Benchmark: 150000 - 210000 CHF Yearly CHF 150000.00 210000.00 YEAR
Job Description & How to Apply Below

All Job Posting Locations:
Allschwil, Switzerland, Schaffhausen, Switzerland, Zug, Switzerland

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 Med Tech, 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  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:
Allschwil, Switzerland, Schaffhausen, Switzerland, Zug, Switzerland

Job Description Principal Engineer, Device & Packaging Technical Launch Integrator (TLI) (f/x/m)

Enabling access to and delivering our new product pipeline to customers and patients globally is a high priority for Johnson & Johnson Innovative Medicine and the Schaffhausen Launch & Grow site. We are looking for an experienced colleague who combines strong device and packaging technical expertise with project leadership and an end-to-end mindset
. Together, we strive to bring innovative combination products and packaging solutions successfully into our commercial supply chain. In this role, you will work within the Local Launch team of the MSAT Biotherapeutics Platform. As a Device & Packaging Technical Launch Integrator (TLI), you will provide technical leadership for the transfer, industrialization, validation, and launch of device and packaging solutions at commercial scale.

Key Responsibilities Device & Packaging Technical Leadership
  • Act as the MSAT Device & Packaging technical lead for assigned new product introduction and technology transfer projects.
  • Lead global and local cross-functional project teams and represent MSAT Device & Packaging within the value chain team and project development teams.
  • Provide technical leadership across device assembly, secondary packaging, labeling/artwork interfaces, and associated manufacturing processes.
  • Partner with R&D, Supply Chain, Quality, Regulatory, Engineering, Procurement, manufacturing sites, and external suppliers to translate product and design requirements into robust commercial manufacturing solutions.
  • Ensure appropriate specifications, controls, and technical requirements are established for device components, packaging materials, and associated processes.
Design Transfer, Industrialization & Validation
  • Lead the design and technology transfer of device and packaging solutions into the commercial manufacturing environment.
  • Drive development, implementation, scale-up, qualification, and validation of device assembly and packaging processes at commercial scale.
  • Partner closely with project and equipment engineers to ensure manufacturing equipment is appropriately designed, tested, installed, qualified, and ready for routine production.
  • Lead technical problem solving and risk management throughout transfer, qualification, validation, and launch.
  • Ensure solutions are robust, manufacturable, compliant, and capable of supporting reliable commercial supply.
Launch Readiness & Project Leadership
  • Drive Device & Packaging activities from project initiation through technical transfer, PPQ/validation, regulatory submission readiness, launch, and handover to the receiving organization.
  • Establish clear project plans, deliverables, risks, dependencies, and milestones for the Device & Packaging workstream.
  • Proactively identify technical and project risks and drive mitigation and escalation where required.
  • Provide regular updates to project stakeholders and sponsors through reports, presentations, governance meetings, and ad-hoc communication.
  • Work closely with the manufacturing-site organization to ensure successful project execution and operational readiness.
  • Ensure technical deliverables supporting health-authority submissions and launch readiness are completed on time and with the required quality.
Technical Documentation & Compliance
  • Deliver a robust technical transfer documentation package in accordance with…
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