LifeSciences Master Graduate // Johnson & Johnson

Job content

Caring for the world, one person at a time. inspires and unites the people of Johnson & Johnson. 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 Companies work with partners in health care to touch the lives of over a billion people every day, throughout the world. We have more than 265 operating companies in more than 60 countries employing approximately 120,000 people.Janssen Vaccines, one of the Janssen Pharmaceutical Companies of Johnson & Johnson, is a global biopharmaceutical company dedicated to bringing meaningful innovation to global health. We do this by discovering, developing, manufacturing and marketing products that combat major threats to the health of people worldwide. The Bern site, with its approx. 600 people of over 25 nationalities, acts as a center of expertise for development and manufacturing of innovative cell based viral- and bacterial vaccines and bacterial based therapeutic products.Main Responsibilities

• Execution of the practical project work within a cGMP regulated environment. To a lead technician an implicit lead function in process execution can be assigned.
• Carry out core Fill and Finish processes (manual and automated aseptic filling, visual inspection, equipment preparation)
• Carry out development and manufacturing activities according to predefined study plans or batch records complying to the defined timelines.
• Generation and update of manufacturing and process supportive documentation.
• Document the executed work in protocols and batch records in accordance to good documentation practice.
• Review filled out batch records and manufacturing protocols.
• Plan the execution of work packages and manufacturing operations as well as side activities.
• Take part in establishment and provide feedback to study plans, study reports, work instructions, batch records, technical and equipment maintenance/calibration reports.
• Internal organization of assigned manufacturing suites including implementation of safety relevant procedures as well as house-keeping activities (log books, cleaning protocols, etc.) in accordance to cGMP regulations.
• Reporting of non-conformances and initiation of quality issue records and low impact investigations as well as corrective actions under cGMP.
• Implementation and introduction of new processing techniques and manufacturing equipment and/or coordination of equipment improvements and modifications.
• Support preparation of engineering specifications and documentation for simple manufacturing equipment; communication with external parties for purchasing of and commissioning of new equipment
• Support Qualification and Validation activities related to Fill&Finish processes, equipment/ rooms
• Support Transfer and Shipment of manufactured product
• Organization and Oversight production related process (e.g. sample management) with other departments

Who we are looking for

• Masters degree within the area of Biotechnology, Food Technology, Biology or similar
• Knowledge of aseptic processing and visual inspection is a plus
• Flexible team player with the ability to prioritize
• Accurate working and documentation style
• Good communication in English and German

This job based in Bern, Switzerland will initially be limited to approx. 12 months. 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!