GMP Supporter

at  Novo Nordisk

GMP Supporter
Category: Manufacturing
Location:Hillerød, Capital Region of Denmark, DK
Would you like to contribute to ensuring a sky-high level of quality in the production of life-saving medicine? Do you dream of using your analytical approach to tasks? Are you keen on preparing documentation subject to strict compliance requirements?
Then you will thrive as our new GMP Supporter. Apply today for a life-changing career!

QUALIFICATIONS

To be successful in this role, we imagine that you have:

• A minimum of a bachelor’s degree in pharmacy, chemical engineering, biochemistry, or a similar field.
• Strong interest in being on the front line and helping colleagues with challenges across the organization and the ability to prepare documentation respecting a very high standard of quality.
• Full professional proficiency in English and Danish.

On a personal level, you quickly gain an overview of complex processes and solve issues in a systematic and data-driven manner. Amazing communication skills enable you to express concisely when documenting events related to the production lines.
Taking the lead, maintaining responsibility and initiative in solving challenges to improve the production line is crucial in this role. Being a team player, who meets deadlines while ensuring our quality is uncompromised, while thriving on following procedures and adhering to standards are key to succeed in this team.

Your main tasks will include:

• Handle deviations and customer complaints, review batch documentation.
• Perform Standard Operation Procedure (SOP) updates and optimisation projects.
• Participate in phone duty approximately every 8 weeks, providing 24/7 guidance for quality issues in production

To be successful in this role, we imagine that you have:

• A minimum of a bachelor’s degree in pharmacy, chemical engineering, biochemistry, or a similar field.
• Strong interest in being on the front line and helping colleagues with challenges across the organization and the ability to prepare documentation respecting a very high standard of quality.
• Full professional proficiency in English and Danish