Gmp Professional, Måløv

Denmark, Denmark, Måløv
Udgivet 2024-05-16
Udløber 2024-06-16
ID #2156351166
Gmp Professional, Måløv
Denmark, Denmark, Måløv,
Udgivet May 16, 2024


Are you passionate about having a central role in a dynamic department with tasks that involve close collaboration with many stakeholders on a daily basis? Do you have a solid understanding of Quality, Good Manufacturing Practice and Training? If yes, you might be exactly the one we are looking for to join our team as a Good Manufacturing Practice Professional, apply today! The Position As a GMP Coordinator at Novo Nordisk, you will play a crucial role in maintaining the department’s quality level.

Your responsibilities will include: Ensuring a high-level GMP overview within the department Participating in authority inspections and internal audits Working in the Quality Management System – Delivery to Quality Management Review (QMR) Handling and disputing Deviations (DV) and Change requests (CR) Taking responsibility for our DV board across the department Keeping track of quality Key Performance Indicators (KPIs) Acting as a superuser in relevant quality systems such as Veeva Vault Quality Docs, Novo Glow, and Q-tracker You will be part of a network of other GMP and training coordinators in Oral Finished Product (OFP), collaborating with the management team to ensure our quality and training targets are met.

Qualifications To succeed in this role, you should have the following qualifications: A BSc or MSc in natural science, engineering, or a similar field At least a couple of years of experience in the pharmaceutical industry or other regulated areas Familiarity with complex quality processes and experience in GMP-regulated areas Technical understanding of IT and systems, in relation to GMP, is an advantage Strong communication skills and the ability to collaborate with various stakeholders across departments Fluency in both Danish and English Experience with LEAN is an advantage, as it is an integral part of our everyday life.

As an individual, you possess the ability to interface at all levels within the organization and excel at solving tasks pragmatically, involving key stakeholders.

It is essential that you can think and act with a broad and holistic perspective while paying attention to important details.

About the department The GMP Coordinator role is part of the OFP Production & Business Support area, which is a newly established area within OFP Denmark.

The area consists of approximately people divided into three departments: Technical Support, Warehouse Support, and Business Support.

OFP is a business area located in two different production buildings, with approximately people.

We are establishing a new team “Sustainability & Skills” with focus on setting the direction and executing our strategy within Circular for Zero, Health & Safety and training within OFP DK.

We have a Triple Bottom Line ensuring focus on environmental and social responsibility as well as economic.

We minimize impact on the environment and have a very ambitious environmental strategy with a “Circular for Zero” ambition.

Working at Novo Nordisk At Novo Nordisk, we don’t wait for change.

We drive it.

We are a dynamic company in an even more dynamic industry, and we know that what got us to where we are today, is not necessarily what will make us successful in the future.

We cover the spirit of experimentation, striving for excellence without fixating on perfection.

We never shy away from opportunities to develop, we seize them.

From research and development to manufacturing, marketing, and sales – we’re all working to move the needle on patient care.


Jobtype: Fuld tid
Kontrakttype: Permanent
Løn type: Månedlige
Beskæftigelse: Gmp professional

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