MSIT Engineering Role in Late Stage Development

Vor 3 Tagen

Bern, Bern, Schweiz Randstad - Medium prio Vollzeit

The Johnson & Johnson Family of Innovative Medicine offers a challenging opportunity for a MSIT Engineer to work with partners in health care and touch the lives of over a billion people every day. Located in Bern, Switzerland, this role is part of the Manufacturing Science Innovation & Technology team and will be based initially for 12 months with possibility of extension.

Main Responsibilities

This multidisciplinary role involves executing project activities in different areas of new biopharmaceutical processes in the Late Stage Development department. As a MSIT Engineer, you will be responsible for covering priority activities in validations, qualifications, cleaning or monitoring studies, zone concepts and other MSIT Drug Substance or Drug Product activities.

You will 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 are interested in learning about GMP processes from all angles and looking for a diverse role in different areas of expertise, this job may be suitable for you.

Key responsibilities include:

  • 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

Functie-eisen

We are looking for a Master Bachelor Degree holder 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 is required, along with flexibility, prioritization, communication skills in German and English. Analytical thinking and problem-solving ability are also necessary.

The estimated annual salary for this position is around €95,000 - €110,000 depending on location and experience. This job offers a unique opportunity to work with a global leading pharmaceutical company in a dynamic, progressive and collaborative environment.

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