CVP GMP Partner

Are you passionate about compliance, structure, and continuous improvement, and possesses a self-motivated, structured, and efficient nature?

We are on the lookout for an experienced candidate with proven track record of identifying solutions in a broader perspective and setting clear direction and have demonstrated a commitment to making a significant difference.
 

Apply now and join our team as CVP (Corporate Vice President) GMP Partner within Biotech and Rare Disease (BRD) based in Gentofte
 

The position
As our new CVP GMP Partner, you will be a part of BRD, Finished Production (FP) management group, referring to the CVP. You will be responsible for supporting the departments within BRD FP to ensure they are continuously improving compliance and delivering on all relevant GMP requirements.
 

You will also play an important role of supporting the GMP coordinators to ensure a high level of quality and compliance in our FP areas in Gentofte, Kirke Værløse and Kalundborg by setting high standards, identifying, scoping, and driving compliance improvement initiatives while maintaining our Quality Management System (QMS).
 

You will be responsible for:

Coordinating preparation for audits and inspections, including planning, organisation and execution and follow-up, providing ad hoc consultation on quality and compliance improvement ideas and challenges. Supporting compliance with GMP and NN QMS. Developing and maintaining quality oversight systems to identify trends and propose relevant actions. Ensuring high-level GMP overview and reporting quality trends to management. Driving continuous improvement of quality performance and processes. Ensuring the maintenance of a productive and efficient GMP coordinators network, which will facilitate collaboration, alignment, and the sharing of best practices for GMP-related tasks across BRD FP.

Qualifications
Your experiences include: A degree in a scientific field such as Pharmacy, Sciences, Engineering, or relevant.

5+ years of experience in a similar position within pharma GMP production. Experience within Finished Production/ QA is advantageous including Quality Management Review. Audits and inspections. A LEAN mindset with experience in systematic problem-solving. Full proficiency in oral and written English.

As a person, you have excellent interpersonal and collaboration skills with the ability to set direction. You thrive solving tasks and challenges as close to the process as possible and working cross functionally with stakeholders at all levels.
 

You are solution-oriented, and you work systematically and proactively while striving for simplicity in processes. You take thrive solving tasks close involvement of your stakeholders.

About the area
BRD is part of Novo Nordisk Product Supply, which is a global production network at the forefront of technology and in quality production of pharmaceutical products. In BRD we are not only supplying all Novo Nordisk products for Rare Diseases, but also using our competences in Biotech to support the growing efforts into completely new production platforms and therapy areas for Novo Nordisk. We are app. 2500 colleagues committed to drive change for people with serious chronic diseases.

We produce our life-saving medicines out of five state-of-the-art production sites in Denmark and United States - covering the entire production value chain where raw materials are cultivated, purified, formulated, filled, assembled in devices, packed, and distributed across the globe. Not only are we making a difference for patients – we are also stiving to make a difference for our employees by promoting a learning culture with high level of trust, innovation, and development for everyone. Are you ready for a life-changing career?
 

---