Job Description:

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.

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 pack operations at J&J Innovative Medicine Schaffhausen. We have recently established a new team focusing on the deployment of innovative digital tools and shop floor technologies.

Position Summary:

You will lead cross-functional project teams to prepare and execute the deployment of innovative technologies, e.g. in the area of Process Analytical Technologies (PAT) and Advanced Process Control (APC) to the manufacturing shop floor. You will help to define technology deployment strategies and actively shape your own role. You will also act as Site MSAT representative in technology projects that are still in the development phase.

Responsibilities:

• Site MSAT Subject Matter Expert for Process Analytical Technologies (PAT), Advanced Process Control (APC) projects and Real-Time-Release (RTR)
• Lead technology deployment projects and actively support technology development projects as a core team member and Site MSAT representative
• Engage with cross-functional stakeholders to define and realize technology deployment strategies
• Lead Change Controls and provide assessments to Change Controls/CAPAs and Deviations as technology owner during life cycle and act as technology single point of contact
• Support definition of standard processes, documentation templates and best practices
• Present project updates and strategies in different forums incl. leadership meetings and steering committees
• Active participation in health authority inspections as Subject Matter Expert
• Maintain excellent partnership with all business partners

Qualifications:

• You have successfully completed your university studies in Engineering, Chemistry, Pharmacy or equivalent and have already gained at least two years of experience in the pharmaceutical industry, ideally with past proven field experience in parenteral manufacturing processes.
• You have proven experience in project leadership and execution preferably in the live science and GMP environment. In addition to that you prefer an independent, self-initiative and goal-oriented way of working to apply your expertise and foster collaboration to reach fast paced goals according to management expectations and project schedules.
• Your strength is decision making and problem-solving, combined with excellent communication skills to represent MSAT in multi-functional and cross-sites teams within the global matrix organization.
• You are open to new ideas, and you drive innovation.
• Proficient in both English and German is required.