GMP Partner

Are you curious to use your quality knowledge, experience, and mindset in an exciting organization working with implementation of analytical methods and new technology? Do you have a systematic approach and focus on details? Would you enjoy being responsible for keeping overview of our Quality and training related tasks?
If yes, then apply now and join us for a life-changing career! The Position
As GMP Partner for our department you will be working to ensure a high level of quality and compliance, by setting the right standards in maintaining our Quality Management System (QMS), so that we continuously deliver on all relevant GMP requirements while at the same finding the right balance where GMP to the highest standard is not required. The same approach will be relevant when you ensure that we all have the necessary and sufficient training assigned. Also, you will have the opportunity to develop and improve our training. Additionally, you will be collaborating closely with many great colleagues within the department, across Biotech & Rare Disease (BRD), Manufacturing Development departments, and in QA.
You will be responsible for:
• Ensuring high-level GMP overview and report quality trends to management.
• Driving preparation for and follow-up on authority inspections and internal audits
• Leading and coordinating critical quality issues and compliance activities in the department and across if necessary.
• Working in the QMS – Delivery to Quality Management Review (QMR).
• Supporting daily operations and ensure the relevant level of GMP in the department.
• Participate when we are involved in audits and inspections.
• Support to us all on being assigned to the relevant training.
As part of your responsibilities, you will run smaller compliance projects in the department and conduct the training of new employees in GMP.
Finally, you will join a harmonious team and department with competent, caring, and positive colleagues. We have a strong foundation of employees with high seniority mixed with more recent newcomers. Novo Nordisk is a great place to work, and our internal engagement survey scores are well above average.
Qualifications
• Masters' degree in pharmacy, biochemistry, production engineering or similar
• At least 3 years of GMP experience from the pharmaceutical industry (Manufacturing/QC/QA)
• Strong understanding of GMP regulations and requirements
• Excellent communication and interpersonal skills
• Ability to work independently with a pragmatic mindset.
• Experience with project management.
• Ability to manage multiple projects and priorities.
• Full professional proficiency English, Danish is an advantage, but not required.
On a personal level you thrive and get motivated by working with and across all levels in the organization, whilst you enjoy great collaboration and communication and setting direction. Additionally, you are solution oriented and work systematically with a pragmatic approach and strive for simplicity in processes. About the Department
Our department is part of BRD Manufacturing Development also known as MSAT (Manufacturing, Science and Technology), and we are situated in Gentofte close to Copenhagen. We are around 65 colleagues who are responsible for supporting QC with new analytical technology and automation, we validate analytical methods during transfer from CMC to QC, we manage the analytical part of BRD projects when new products are handed over from CMC and throughout life cycle management, we ensure excellent internal and external analytical documentation of our products, and we ensure presence and documentation of reference materials for all BRD products. A complex and fantastic department to work in. Working at BRD, Novo Nordisk
BRD is part of Novo Nordisk Product Supply, which is a global production network at the forefront of technology and quality production of pharmaceutical products. In BRD, we are not only supplying all Novo Nordisk products to people living with serious chronic diseases, but we also use our competences in biotech to support the growing efforts into completely new production platforms and therapy areas for Novo Nordisk.
We are more than 3000 dedicated colleagues working at six production sites in Denmark and the United States. Here we cover the entire production value chain where raw materials are cultivated, purified, formulated, filled, assembled in devices, packed, and distributed across the globe. As more and more people need our products, we support Novo Nordisk's initiatives in new therapy areas. Every day, we work to streamline and expand our capacity through process innovation, automation, and the introduction of new technology. Contact
If you want to hear more or have questions, please do not hesitate to contact Lasse Lollike at +45 30 79 54 35. Deadline
15 November 2023.
Please note that interviews will be held throughout the period, and we encourage you to apply as soon as possible.

You do not need to attach a cover letter to your application, but please include a few sentences about why you are applying in your resume. To ensure an efficient and fair recruitment process, please refrain from adding a photo in your CV. We commit to an inclusive recruitment process and equality of opportunity for all our job applicants. At Novo Nordisk we recognize that it is no longer good enough to aspire to be the best company in the world. We need to aspire to be the best company for the world and we know that this is only possible with talented employees with diverse perspectives, backgrounds and cultures. We are therefore committed to creating an inclusive culture that celebrates the diversity of our employees, the patients we serve and communities we operate in. Together, we’re life changing.