Glycom A/S · Publicerad 20 feb

he job and ideal candidate

We are looking for an ambitious Regulatory & Scientific Affairs Manager with strong scientific education, excellent scientific writing skills and experience in food regulatory affairs.

The ideal candidate fulfils the following expectations:
  • Holds a degree (BSc, MSc or PhD) in a scientific discipline related to nutrition, toxicology or biotechnology; and potentially in addition a degree in food regulatory affairs (PgDipl, BSc or MSc)
  • And/or has several years of practical experience in related fields (e.g. regulatory affairs, toxicology, food legislation, scientific writing, governmental food authorities)
  • Possesses demonstrated excellent scientific writing skills
  • Possesses multidisciplinary understanding of science, technology and legislation
  • Possesses excellent Microsoft Office and general software skills (experience with SharePoint or other data management systems is a Plus)
  • Is perfectly fluent in English and has strong interpersonal skills in order to collaborate with people on all levels and from different cultural backgrounds
  • Has potentially additional language skills relevant to target markets (i.e. Mandarin, Spanish, Portuguese, French, Malay), which are a Plus but not a requirement.
You are a team player, have drive and tenacity, and are able to work in a structured and systematic way to tight deadlines whilst keeping a cool head and a positive approach. You will be reporting to the Head of Regulatory Affairs and your key responsibilities are as listed below.

Responsibilities will include:
  • Identify and assess regulatory risks associated with product development and define plans with project teams to mitigate the risks
  • Maintain an awareness of new and developing legislation, regulatory policy and regulatory guidance relating to food and food ingredients, mainly in the EU
  • Prepare regulatory dossiers for food and food ingredient submissions globally
  • Interact with analytical and project teams to understand, assess and collect information relevant to regulatory submissions
  • Support data and document archiving relevant to regulatory applications
  • Initiate and supervise external work (mostly of analytical nature) to fill data gaps.
Other tasks may be applicable according to candidate's skillset.

Salary and terms of employment

This is a permanent and full-time position. Salary in accordance to your qualifications. You will be based in Scion DTU Science and Technology Park in Hørsholm (20 km North of Copenhagen).

Application

Please send your application and CV via StepStone and kindly indicate your earliest availability. If you wish to learn more about the job, please get in touch with Christoph Röhrig, Head of Regulatory Affairs (christoph.roehrig@glycom.com; +45 2826 3724). Please apply via StepStone as soon as possible as we review applications on an on-going basis.

For further information about Glycom please visit www.glycom.com or follow us on LinkedIn.
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Om företaget
Glycom A/S is a young and vibrant Danish biotechnology company focused on the production of human milk oligosaccharides (HMOs). We are the world leader in this field and have an ambitious program to develop a deeper understanding and application of HMOs to benefit human health. Glycom employs a successful, multinational science and industrial production team, who specialize in fermentation biotechnology, carbohydrate chemistry and human biology. Our leading HMO products are approved in the EU and the US, including as infant formula ingredients, and we seek approval in further global markets, additional applications and for new ingredients.
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Sista ansökningsdag
21 apr
Ort
Utland
Anställning
Tillsvidareanställd
Omfattning
Heltid
Antal Tjänster
1
Yrkesområde
Teknik & Ingenjör