Contract Manufacturing Supply Chain Supporter

Are you passionate about supply chain management and ensuring GMP compliance? Do you enjoy working with projects, with many different external stakeholders? We are seeking an enthusiastic and detail-oriented Contract Manufacturing  Supply Chain Supporter with a specific focus on GMP (Good Manufacturing Practice) documentation. Apply today and join our team!  

The position 

As our new Contract Manufacturing Supply Chain Supporter, you will play a pivotal role in our newly established Contract Manufacturing Team. The team is ensuring that GMP documentation requirements for suppliers are meticulously managed and in compliance with industry standards. You will be responsible for driving or supporting process improvement projects across the organization and locally in the team. You will act as work package owner (WPO) and participate in projects implementing CMO’s.  

Your responsibilities will include: 

• Work closely with the Contract Manufacturing Supporters to support the management of a specific category of products or services. 
• Collaborate with internal and external stakeholders to ensure that documentation requirements for suppliers align with GMP standards and are efficiently managed. 
• Assist in the evaluation and selection of suppliers, considering their adherence to GMP documentation requirements, and participate in contract negotiations. 
• Monitor and maintain a robust documentation system to track supplier GMP compliance, ensuring accuracy and completeness of records. 
• Contribute to the development and implementation of strategies to improve GMP documentation processes and enhance overall supplier compliance. 

Qualifications

• Bachelor's degree in Business Administration, Supply Chain Management, Life Sciences, or a related field. 
• Minimum of 2 years of experience in procurement or supply chain management, with a focus on GMP documentation within a regulated industry. 
• Strong understanding of GMP standards and documentation requirements, with the ability to ensure supplier compliance and maintain accurate records. 
• Excellent communication skills, with the ability to collaborate effectively with cross-functional teams and external stakeholders. 
• Detail-oriented and organized, with the ability to manage complex documentation processes and ensure accuracy and completeness. 

About the department 

Novo Nordisk Pharmatech A/S is a fully owned subsidiary of Novo Nordisk A/S situated in Køge. Novo Nordisk Pharmatech A/S is a leading global supplier of high-quality ingredients for the biopharmaceutical and pharmaceutical industries, supplying products such as recombinant insulin for cell growth media and pharmaceutical grade quaternary ammonium compounds as well as raw materials for Novo Nordisk A/S. 

The Contract Manufacturing team consist of 8 dedicated colleagues that cover different areas of responsibilities like: Sourcing, material, supplier implementation, GMP documentation, tech transfer, CMO screening and selection and contract negotiations.  

Working at Novo Nordisk Pharmatech  

Novo Nordisk Pharmatech A/S has approximately 500 employees and is 100% owned by Novo Nordisk A/S. The ability of Novo Nordisk Pharmatech A/S to produce and deliver quality products to the pharmaceutical industry, combined with our complete range of services within the regulatory requirements, makes us a preferred supplier to many global pharmaceutical companies. Novo Nordisk Pharmatech A/S is a growing company, which will provide many exciting projects in the future and good development opportunities in the job. 

Contact 

For further information, please contact Senior Manager in Contract Manufacturing, Dorthe Christensen at +45 31 97 00 32 

 Deadline 
11 December, 2024.  

We will screen applications on an ongoing basis, so please apply as soon as you can.  
You do not need to attach a cover letter to your application, but please include a few lines about your motivation in your resume or CV. In addition, please avoid the use of photos in your CV. This improves the process by reducing bias. 

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.