GMP Coordinator

Are you interested in working with processes, problem solving, inspections and data? Do you want to share knowledge of Good Manufacturing Practice (GMP) and making an impact in our Warehouse (WH)? Do you feel motivated by setting high compliance standards and ensuring that we continuously improve our processes and ways of working? Warehouse

Then you might be our new GMP coordinator Apply today for a life-changing career

The Position
As GMP coordinator, you will be part of management and have close collaboration with the local Warehouse teams. The dynamic workday consists of problem solving, risk assessments, audit and inspections and input to project across site GE.

Everyday life will be filled with setting the standard for the daily GMP operations together with the WH support team, keep track on GAPs and GMP actions, support WH activities in minor and major local projects, and collaboration with GMP coordinators across the CVP area to set direction for the compliance level at site Gentofte.
 

The main task will be to:

• Set the standard for the GMP compliance level in the local WH.
• Prepare, handle and coordinate audit and inspections together with GMP coordinators in the CVP area.
• Drive and implement major operational tasks - e.g. requirements from authorities, new equipment, major change cases and deviation handling, with a focus on continuous improvement and optimizations.
• Participate in and conduct risk assessment for WH activities for projects.

Qualifications

To be considered for this position, you should have:

• A min. bachelor`s degree in manufacturing, pharmaceutical engineering or similar field.
• Extensive, proven knowledge of GMP and work experience as a supporter or GMP coordinator in production or Warehouse, preferably with minimum 4 years of experience.
• Knowledge or experience from operations and development within Warehouse, production, supply chain, or other relevant functional areas.
• Fluency in written and spoken Danish and English.

On a personal level, you are  adaptable and ready to reprioritize tasks while being able to communicate with various stakeholders across the organization. You are structured, service-minded and committed to work while being able to complete tasks before deadline. You can communicate complex issues in a simple and understandable way to both management, supporters and operators. 
Thriving on working with processes, problem solving, data in Excel, and give input to validations/qualifications, all while bringing strong quality and compliance mindset is crucial in this role.

We will welcome a colleague who is positive, solution-oriented, outgoing and a team player, with good interpersonal skills and good sense of humor. Having a high degree of independence, being ambitious and structured, while always persisting at a can-do attitude and a curious and pragmatic approach is an essential part of this role.

About the department
You will be part of Warehouse leadership where we prioritize time for sparring, knowledge sharing and are always willing to give each other a helping hand if needed. We are a social team that makes room for diversity and sees the strength in each other's differences

Warehouse is part of the Business Support department in Aseptic Manufacturing, Gentofte, and we support our manufacturing areas across Gentofte. The co-teams in the department are responsible for LEAN & Operational Excellence, Digitalization, Manufacturing Intelligence & Business Intelligence, Planning & Capacity, Training and Finance & Procurement.
In the department we are ambitious and strive to deliver the best possible services to our production departments. To help you do this, we will guarantee you a lot of sparring and development feedback. And we make sure to have fun while we drive the business forward.

Working at Aseptic Manufacturing Gentofte, Novo Nordisk
Aseptic Manufacturing site Gentofte is part of the global Product Supply Aseptic Manufacturing network. At our sites across Gentofte, we are more than 700 colleagues responsible for the aseptic manufacturing where we are transforming the API (Active Pharmaceutical Ingredient) into finished products for people living with serious chronic diseases. We work with advanced processes such as formulation, filling, and freeze- drying in a sterile environment. We bring value to our patients by delivering high-quality products in compliance with GMP (Good Manufacturing Practice) in a timely and cost-effective manner as we constantly optimize our processes and invest in new technology.

Contact
For further information, please contact Serap Sahin (Senior Manager) OPSI@novonordisk.com 

Deadline

17 November 2024

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.