MSAT Senior Engineer Device Assembly & Packaging (100%)

“Caring for the world… one person at a time” inspires and unites the people of Johnson & Johnson. This culture of caring is the focus of our corporate philosophy, that are anchored in the internationally applicable Credo. Come and join us to create a future where disease is a thing of the past. Johnson & Johnson Innovative Medicine Schaffhausen Site/Cilag AG is a Launch site for new products with focus on Parenteral Products (e.g., pre-filled syringes and vials).

We belong to the Manufacturing Science & Technology (MSAT) organization for the MTO (Manufacturing and Technical Operations) Large and Small Molecule Manufacturing Platform. We support the Parenteral small and large molecule filling, visual inspection, device assembly and packaging operations at J&J Innovative Medicine Schaffhausen and currently we are looking for a passionate, highly motivated and inclusive packaging engineer supporting our mission to deliver best in class results for our patients.

MSAT Senior Engineer Packaging (100%)

Position summary:

You will be the Site MSAT representative on multi-functional teams supporting process validations of device assembly and packaging processes as well as technical implementation of print templates of all secondary packaging components for all pharmaceutical products packed at the Schaffhausen Fill Finish site.

You will provide the following:

• Technical support and leadership to top line growth


• Ensure reliability, compliance & efficiency of product value chains end to end


• Integrate Manufacturing Operations and Pharmaceutical Development in partnership with Product and Customer Management

Principal responsibilities:

• Site MSAT SME for Device Assembly, Packaging and Artwork Coordination.


• Accountable to meet project timelines during qualification and validation of device assembly and packaging lines and related processes.


• Own and coordinate technical changes of print templates for pharmaceutical secondary packaging components (labels, boxes, inserts) as part of and qualification activities.


• Support validation activities with internal partners as part of multi-functional project teams.


• Deliver on strategic project goals and process improvements to ensure competitiveness at the pharmaceutical market and with global players.


• Provide Technical Assessments to Change Controls/CAPAs and Deviations.


• Active participation in health authority inspections.


• Maintain excellent partnership with all business partners.


• Perform statistical analyses on production data.