C&Q Engineer

Highly Competitive
  1. Permanent
  2. Project Engineering
  3. Switzerland
Bern, Switzerland
Posting date: 25 Feb 2025
64402

Join the team and be part of an innovative company that values inclusion, growth, and impact. Our dynamic work environment offers brilliant opportunities for advancement. We're seeking talented and driven individuals who share our passion for making a difference within the Life Science industry.

Please note that to be considered for this role you must have the right to work in this location or hold an EU passport.


The Client

  • For us, it is all about improving and saving lives
  • We are a fully integrated vaccine company focused on the development, manufacturing, and commercialization of vaccines, and our vision is to become one of the largest pure-play vaccine companies in the world. At the client, you will be part of a global team of +1600 dedicated colleagues worldwide, all passionate about making a difference. We offer an inclusive and flexible workplace with a strong focus on personal and professional development, and we welcome people who are passionate about saving lives. If you are open-minded and have the willpower to succeed, we might just be a perfect fit.
  • At the client Berna, the Swiss affiliate there are - beside manufacturing activities - professionals in Quality Assurance, Quality Control, Supply Chain and Regulatory affairs working. On the Swiss site of Emergent in Thörishaus / Bern there are approx. + 200 dedicated and committed professionals working locally and globally.
  • We are looking to strengthen the Engineering Team with an Engineer Commissioning & Qualification (f/m/d)

Key responsibilities

  • Supervise and perform commissioning of biopharmaceutical systems and equipment.
  • Ensuring all systems and components are installed according to the specific requirements of the biopharmaceutical industry.
  • Perform functional testing and qualification testing to ensure systems are functioning properly and according to user requirements.
  • Identify and resolve qualification issues and non-conformances in collaboration with the quality management team.
  • Implementing process improvements and continuous improvements of qualification strategies.

Requirements

  • Academic education (university, university of applied sciences) in the field of mechanical engineering, process engineering, biology, biotechnology, pharmaceutical technology, chemistry or comparable or extensive professional experience in the field of biopharmaceutical technology.
  • Experience in the biopharmaceutical industry under GMP production conditions.
  • Written and spoken German and English.
  • Initiative, ability to work under pressure, decision-making ability, judgment, independence, conscientious way of working.
  • Good communication skills, team-oriented way of working and a high sense of responsibility round off your profile.

If you are having difficulty in applying or if you have any questions, please contact Ashley Bennett at a.bennett@proclinical.com.



Apply Now:

If you are interested in learning more or applying to this exciting opportunity, please complete the form below and attach a copy of your CV. Alternatively, for further details or to talk directly to a life sciences recruitment specialist, please request a call back at the top of this page.

Proclinical is a leading life sciences recruiter focused on finding exceptional people and matching them with the finest positions across the globe. Proclinical is acting as an Employment Agency in relation to this vacancy.

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