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UDLØBET

Novo Nordisk

Advanced QA Release Engineer

Fuldtid

Permanent

Stenager Alle 4, 9800 Hjørring, Danmark

SE PÅ KORT
ID: 2744345
|
Indrykket for 73 dage siden

Do you enjoy critical thinking, innovation and problem solving? Are you passionate about ensuring the delivery of high-quality medical products to patients? Do you thrive in a collaborative environment where teamwork is a key to success?
If so, consider becoming a vital part of Novo Nordisk's Quality Assurance (QA) department within Global Contract Manufacturing (GCM) Devices, External Batch Release in Hjørring. Read on to learn more and apply now! 

The Position
We are on the lookout for an Advanced QA Release Engineer with good communication skills, continuous improvement mindset and the desire to work closely together with a lot of different stakeholders.

As our new colleague within batch release your main tasks will involve:
• Review documentation and release components and needle products from our suppliers and contract manufacturer. 
• Working with GMP and documentation tasks.
• Having an eye for detail and a strong quality mindset to perform daily tasks. 

You thrive with routine tasks and maintain focus in an environment where priorities can change rapidly. The position calls for your ability to be self-driven, but at the same time understand the importance of teamwork. 

Qualifications
We expect our ideal candidate to have the following:
• Master’s degree in Science or other relevant field.
• A background that provides you with a solid technical understanding for QA (preferably from a GMP production environment as a QA or Process Engineer). 
• 1+ yrs of experience working with GMP and documentation.
• IT knowledge or technical flair and an interest to expand your knowledge within this are. IT knowledge may include e.g. SAP, Digitalised Batch Release (DBR) and LIMS. 
• Ideally, you have knowledge of requirements for production records and good documentation practise, and you have an understanding for simplicity in these processes. 
• Proficiency in Danish and English, both oral and written.

As a person, you are analytical, systematic and you possess excellent communication skills. You are curious, willing to learn, and good at asking questions, and you can stay engaged in a position where days look similar from time to time.

About the Department
You will be a part of the Quality department of our external needle production and have a workday with a large degree of independence. We are a team of 12 employees responsible for the Quality Assurance of all needle products produced externally by Novo Nordisk. Our main purpose is to safeguard patient safety, product quality and compliance of pen needles and components. You will find that you have rich opportunities to share ideas, create great results and develop yourself, both on a professional and on a personal level.

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