Scientist – Merck KGaA, Darmstadt, Germany

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Work Your Magic with us!

Ready to explore, break barriers, and discover more? We know you’ve got big plans – so do we! Our colleagues across the globe love innovating with science and technology to enrich people’s lives with our solutions in Healthcare, Life Science, and Electronics. Together, we dream big and are passionate about caring for our rich mix of people, customers, patients, and planet. That’s why we are always looking for curious minds that see themselves imagining the unimaginable with us.

 

Your Role: 

 

We have an exciting opportunity for a Scientist to join our Virology team. In this role, you will be responsible for providing scientific support in the conduct of routine and complex GLP or GMP studies performed within a contract testing laboratory. You will act as Study Director or Responsible Scientist, as appropriate, on studies, assisting in the performance of laboratory procedures, providing scientific support to laboratory staff and external clients for whom the work is being performed. You will also be required to maintain study records, including deviation records, to meet regulatory standards. Other duties include preparing documents related to studies, such as SOP’s, technical reports, summaries, protocols, etc., liaising with Commercial Operations, Development Services and Program Management to provide technical support for ongoing and upcoming projects and participating in external and internal client conference calls, meetings and audits. This role forms part of our planned growth in Glasgow and is a pivotal role in Virology – a wonderful opportunity for an experienced professional to join us and develop their career with a business that is going from strength to strength.

 

Who you are:

 

  • You will have an HND or higher in a Biological Science discipline, with competent proven work experience in a similar environment; ideally with Cell Culture experience.
  • Experience in PCR based techniques would be beneficial
  • You will have prior knowledge and experience working to GLP / GMP standards.
  • You are strongly focused on quality and safety and have strong planning and organisational skills
  • You have good communication and interpersonal skills and are self-motivated, with strong initiative and drive
  • You have a good standard of written and spoken English and are computer literate, ideally with prior knowledge of working with LIM

What we offer: We are curious minds that come from a broad range of backgrounds, perspectives, and life experiences. We celebrate all dimensions of diversity and believe that it drives excellence and innovation, strengthening our ability to lead in science and technology. We are committed to creating access and opportunities for all to develop and grow at your own pace. Join us in building a culture of inclusion and belonging that impacts millions and empowers everyone to work their magic and champion human progress!
 
Apply now and become a part of our diverse team!

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