Process Specialist NPI/LCM

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.jnj.com

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About Innovative Medicine

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.jnj.com/innovative-medicine 

Johnson&Johnson's Innovative Medicine is recruiting for a Process Specialist in the Parenterals Manufacturing and Filling Operations organization, located in Schaffhausen, Switzerland.

Purpose:

As a Process Specialist Parenterals New Product Introduction & Life Cycle Management you are responsible for the introduction of new products in our commercial production and implementation of new technologies and processes in alignment with tech transfer plans and business objectives. You will support innovation, cost improvement and compliance projects in parenterals operations and assure robust and reliable process implementation in close collaboration with the operations units. Your responsibilities include support of inspections, filings and health authority responses acting as subject matter expert for production related topics.

Job Responsibilities

• Support of projects in New Product Introduction and Lifecycle Management in the Business Unit Parenterals.
• Support of improvement projects.
• Responsible for change controls, recipe and document changes.
• Training of project related content on the shop floor and in the leadership teams.
• Close collaboration with production as well as with other relevant business partners.
• Follows GMP, EHS and SOX guidelines.

Qualifications

• A minimum of a bachelor’s degree in natural science or engineering is required. Master’s degree preferred
• 2+ years of experience in various fields in Pharmaceutical industry in a role involved in parenteral/pharmaceutical manufacturing or development required.
• Preferably experience with introduction of parenteral products into manufacturing sites (biotechnologically produced and/or chemically synthesized APIs), late-stage development activities as well as technical and process knowledge of manufacturing site unit operations (e.g. compounding, milling, and filling of liquid formulations and suspensions)
• Strong planning and logistics skills to effectively integrate drug product deliverables and execution at the manufacturing level
• Excellent written and oral communication skills and ability to influence partners, peers and collaborators at all levels
• Proficiency in German and English is a requirement
• Ability to work independently with proven problem-solving skills

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