GMP Material Scientist for Raw Material qualification

at  Novo Nordisk

GMP Material Scientist for Raw Material qualification
Category: Manufacturing
Location:Søborg, Capital Region of Denmark, DK
Are you ready for a career in the pharmaceutical industry and join a growing area taking part in the development of the future Novo Nordisk product pipeline? Are you looking for an opportunity to apply and develop your skills within raw materials for GMP production, process, project & stakeholder management? And do you thrive working with high complexity tasks and improvement projects focusing on digital solutions and automated processes?
If yes, then we have the right challenge for you within the expanding GMP Raw Materials team in CMC API Process Operations as our new Development Scientist for Raw Material qualification. Come join us in helping more than forty million patients world-wide.

QUALIFICATIONS

You hold a relevant Master or PhD degree within a field of scientific expertise such as but not limited to Engineering, Biology, Biochemistry or similar. In addition, we are looking for candidates with the following qualifications:

• GMP experience in the pharmaceutical industry preferably from a similar role.
• Coordinating tasks within a large project with many different stakeholders.
• Excellent communication skills and proficiency in both spoken and written English.
• Great collaboration skills with a good sense of priority and not afraid to set direction.
• A team-player who enjoys cross-functional, cross-departmental and stakeholder collaboration.

We are looking for profiles with various levels of seniority and experience. We are open to experienced senior profiles as well as newly graduated profiles with relevant pharmaceutical or manufacturing experience.

• GMP material Qualification of different types of materials (raw materials, consumables, intermediates) including Setting the internal release specification for the warehouse and quality control (QC).
• Close contact and collaboration with various external stakeholders such as material suppliers, logistics services etc., to obtain sufficient knowledge to ensure patient safety, GMP, and GDP compliance.
• Collaboration with internal stakeholders to ensure proper scientific evaluations in documentation packages.
• Participation in supplier assessment and auditing