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Raw Materials Coordinator and Process Owner

Hillerød, Denmark

Do you want to join an advanced biotech company that develop and manufacture some of the leading biological products on the market today and for the future? Then join Fujifilm Diosynth Biotechnologies, a biotech company that aspires to be the leading CDMO within our areas of expertise.

Do you like to coordinate, manage stakeholders, keep timelines, help your colleagues and reinvent processes? Then we have the job you are looking for! We are currently looking for a Raw Material Coordinator for our Regulatory Affairs, Supplier Quality and Audits team.

The team for you to join

You will be part of a great, hard-working and self-managed team of competent colleagues. We are a team of 9 experienced individuals covering a variety of tasks, we are driven by our curiosity, humor and commitment to the patient. We support each other and help where we can.

What would your role look like?

You will own, reinvent and drive/ coordinate the raw material intake process together with stakeholders in QC, Material Science, Supply Chain and Purchasing. Identify improvements and implemented them on the fly to ensure the best possible process for the company of course always in alignment with the stakeholders. Identify appropriate measurement/ monitoring of the process to ensure these are visible to all who are interested, but also to ensure improvements are visible. Basically you will interact with our suppliers, internal colleagues and customers. You will be based in Hillerød together with the team.

A new set of eyes are always welcome and in general you are expected to speak up, be curious and help out if other processes can be improved.

Who are we looking for?

A person with a good sense of humor and charm, who can work independent yet be a team player when it is needed. Experience with GxP requirements and stakeholder skills. You have practical experience with EU GMP and cGMP from various positions within the biotech/ pharmaceutical industry. Excellent knowledge of what it takes to bring in raw materials from a QC, Material Science and GMP point of view.

You must have/ be:

BSc/ MSc degree within natural & life science and several years of relevant GxP experience or you have another background within natural & life science and have broad QC experience for many years and have experience with raw materials, specifications, process optimization and stakeholder management.

Skills to:

  • Reinvent/ improve processes and update relevant SOP’s accordingly
  • Manage stakeholders
  • Measure/ monitor process and progress
  • Run the process, follow up and improve
  • Willing to interact with suppliers, internal colleagues and customers
  • Able to work with it systems, especially TrackWise as most of the practical work will happen in our change control process
  • Able to speak up with data and curiosity

Optional: Medical Device experience and the ability to assess the legislation vs actual process

What we offer you

A company with an amazing culture. Great colleagues in a newly established rapidly growing team. A challenging position with an established CDMO, who is growing rapidly. All the challenges you can imagine and we can promise that you will not get bored!

If you need more information

Contact person: Kristian Byrialsen, Head of Regulatory Affairs, Supplier Quality and Audits. +45 26 24 33 46. (only for applicants)

Please apply online in the HR system, applications received in other ways will not be considered. We are reviewing applications on continuous basis and urge you to apply as soon as possible and latest by 23rd of August.

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