Cultivation Chemist for API Manufacturing Development in Biopharm

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Gentofte

  • Manufacturing
  • Gentofte

Are you ready to make a difference for people living with haemophilia and other rare endocrine disorders? Do you want to work with the development of complex processes and be part of a super engaged team? Then you might be our new colleague in Biopharm API Manufacturing Development.

Use your in-depth mammalian and microbial cultivation expertise to develop our current and our new product portfolio! If you are outgoing and an experienced cultivation chemist, then you can become our new colleague in API Manufacturing and Development.

About the department

Biopharm API Manufacturing Development in Gentofte is part of Biopharm Manufacturing Development, which consists of 43 employees in 3 teams.

You will become part of the team "API Support and Development". The team’s primary responsibility is the entire set of Life-Cycle-Management activities for all Biopharm’s API products. This ranges from Development work for Phase 3 production, regulatory strategy and submissions, innovation (testing and implementing new technologies) and laboratory experiments for e.g. yield optimization.

Our team consists of 18 chemists where three people are currently working with cultivation. As we are expanding our portfolio with new products, we are now looking for a new colleague with a passion for upstream development.

The position

We offer you an exciting position, where you will work with many different tasks within development and support of Biopharm’s cultivation processes. The right candidate will get the responsibility for one or more of Biopharm’s cultivation processes. This includes ownership of the development package, transfer of processes from development to production facilities, creating and keeping central documents as master formulas and IPC updated. Furthermore, you have responsibility for yield and process optimisations including laboratory work in our inhouse laboratory, support for the ongoing production and the responsibility for the regulatory package. Experience with data analysis and processes modelling is an advantage.

You will be part of a team with many stakeholders and therefore communication and collaboration are of key importance to ensure efficient distribution of tasks and alignment across the team and the department. Furthermore, you are expected to build and maintain a good relation to your wide range of stakeholders e.g. the production departments, Quality Assurance, R&D, Regulatory Affairs, senior management groups, analytical departments and project groups.

We work as a team and you will therefore have a broad variety of assignments and great opportunities for developing your skills. Team spirit is important to us and although we like working independently, we believe in succeeding together. We enjoy getting together around social activities, looking out for each other and maintaining a good work-life balance.

Qualifications

We imagine that you hold a MSc in Biotechnology, Chemistry, Biology, or of similar relevance. Preferably, you have 5+ years of experience working with mammalian and/or microbial cultivation. Ideally you have experience from a pharmaceutical production and experience with LEAN and cGMP. Experience in handling regulatory documents will be considered an advantage. In addition, you are fluent in both Danish and English.

Personally, you are outgoing and self-driven – you thrive in an environment where you get to throw yourself in at the deep end, always seizing an opportunity for personal and professional development. Applying your structured, systematic approach, you take pride in identifying opportunities for optimizations, while steadfastly maintaining your delivery focus.

Contact

If you have questions about the job or just want to get a feel for the department and our exciting challenges ahead, please do not hesitate to call Alexander Hildenbrand at +45 3079 3630.

Deadline

07 Sep 2020.

You are welcome to submit your application in Danish or English. Qualified candidates may be interviewed before deadline.

Millions rely on us
To work for Novo Nordisk you will need the skills, dedication and ambition to change lives for the better for millions of patients living with diabetes and other chronical diseases. In exchange, we offer the chance to be part of a truly global workplace, where passion and engagement are met with opportunities for professional and personal development.


Information og data

Denne ledige stilling har jobtypen "Laborant", og befinder sig i kategorien "Sundhed og forskning".

Arbejdsstedet er beliggende i Gentofte.

Jobbet er oprettet på vores service den 20.8.2020, men kan have været deaktiveret og genaktiveret igen.

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Dagligt opdateret: Dette job opdateres dagligt ud fra jobudbyderens hjemmeside via vores søgemaskineteknologi og er aktivt lige nu.
  • Laborant
  • Gentofte
  • Mandag den 07. september 2020
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