MSIT Engineer

vor 1 Monat


Bern, Bern, Schweiz Randstad - Medium prio Vollzeit
Job Description

We are seeking a highly skilled MSIT Engineer to join our team in Bern, Switzerland. As a key member of our Manufacturing Science Innovation & Technology team, you will be responsible for executing project activities in different areas of biopharmaceutical processes in the Late Stage Development department.

Main Responsibilities

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. 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.

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

Requirements

We are looking for a team player with a Master's or Bachelor's degree in Engineering, Biotechnology, Food Technology, Biology or a similar discipline. Work experience in a pharmaceutical company is a major plus. You should have general knowledge of GMP and be able to communicate effectively in German and English.

This is a 12-month contract with the possibility of extension. If you are interested in working with a global leading pharmaceutical company in a dynamic, progressive and collaborative environment, please send us your application today.


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