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 is anchored in the internationally applicable Credo. We embrace research and science - bringing innovative ideas, products and services to advance the health and well-being of people. Employees of the Johnson & Johnson Family of Innovative Medicine work with partners in health care to touch the lives of over a billion people every day, throughout the world. We have more than 260 operating companies in more than 60 countries employing approximately 134,000 people. Our worldwide headquarters is in New Brunswick, New Jersey, USA.

Main Responsibilities

In this multidisciplinary role, you will be a member of MSIT executing project activities in different areas of (new) biopharmaceutical processes in the Late Stage Development department. The MSIT Engineer is responsible for covering priority activities in validations, qualifications, cleaning or monitoring studies, zone concepts and other MSIT Drug Substance or Drug Product activities. This role gives you a broad area of insight and development of unique experience of GMP related MSIT work with new areas and challenges with each new task. You perform technical work under general supervision of experienced Subject Matter Experts, providing you with knowledge of the specific area and expanding your expertise therewith. If you look for a diverse role in different areas of expertise, are interested in learning about GMP processes from all angles, this is the job for you!

Essential duties:

? Collaborate in implementation projects for Drug Substance or Drug Product under GxP for the production of vaccines and other products

? Represent MSIT functions in project teams

? Deliver specific project tasks based on project milestones/priorities based on area of expertise

? Writing documents and supporting document readiness for activities in the production units

? Establish, review and Implementation of process related procedures

? Evaluate product/process performance and deviations, troubleshooting, performance of change activities, tracking and reporting key production and quality indicators against established metrics

? Propose new or improved technologies to enhance product quality, manufacturing cost efficiencies, personnel safety and regulatory compliance

? Collaborate with GMP Operations for investigations, change controls, data verification and process improvements

? Lead specific Qualification and Validation project activities related to manufacturing processes, equipment and cleanrooms

Who we are looking for

? Master Bachelor Degree within the area of Engineering, Biotechnology, Food Technology, Biology or similar discipline

? Work experience in a pharmaceutical company is a major plus

? General Knowledge of GMP

? Flexible team player with the ability to prioritize

? Interest in working in different teams open for challenges and new topics

? Accurate working and documentation style

? Analytical thinking and problem-solving ability

? Good communication in German and English

This job in our Manufacturing Science Innovation & Technology team is based in Bern, Switzerland and will initially be limited to 12 months with possibility of extension. If you are interested in working with a global leading pharmaceutical company in a dynamic, progressive and collaborative environment, then send us your application today. Or give us a call if you have any questions.