Quality Assurance Technician

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

The position
We welcome a QA Technician to join our dynamic team. As our new colleague, you will:

Be responsible for QA batch release for our suppliers around the world.

Provide support for deviation handling and change requests.

Develop and maintain the Quality System, including updating SOPs.

Focus on continuous improvements and streamlining processes.

As part of the [xxxxx] Quality organisation, we prioritise compliance, support the business, and strive to simplify daily work for ourselves and stakeholders.

Qualifications
Your experiences include:

Academic background with 1+ years of experience as QA, Process Engineer, or similar working with product approval/ QC.

Have experience in a pharmaceutical company, preferably within QA, Supply Chain, or Production.

Understand regulations, requirements, and guidelines for GMP production.

IT knowledge or technical flair with a keen interest to expand knowledge within this. IT knowledge may include e.g. SAP, Digitalised Batch Release (DBR), LIMS etc.

Additional advantages include familiarity with ISO13485, GMP, validation, Lean principles, and previous experience in the medical devices sector.

Excellent communication skills in both Danish and English.

As a professional, you see yourself as being curious minded and inquisitive, and enjoy understanding complex processes by interacting with colleagues within the team and with many stakeholders of all levels from various departments. You are structured and organised in your approach to work and thrive working under pressure. You have the ability to stay engaged and focused on details in a position where days look similiar from time to time.

About the department
Global Contract Manufacturing (GCM) Devices, External Batch Release comprises 5 highly qualified colleagues and is responsible for QA of external production and the global supply chain of high-quality components and preassembled parts for all Novo Nordisk prefilled and durable devices. Our external suppliers are located inEurope, China, USA, and Brazil. Our main purpose is to safeguard patient safety, product quality, and compliance.
We work in the welcoming surroundings of [xxxxx] in Hillerød, approximately 30 km north of Copenhagen.

Working at [xxxxx]
At [xxxxx], we always strive for excellence and continuously develop our expertise to stay ahead - both as a company and as individuals. We believe that innovation and creativity thrive in a healthy and engaging working environment. Therefore, we give you the opportunity to bring your personal ambition and passion to work to improve the quality of life of the patients.
Contact
For further information, please contact Associate Manager Sara Dalgaard (Manager, External QA Batch Release) at: +[xxxxx]

Deadline
30 June 2024
You do not need to attach a cover letter to your application, but please include a few sentences about why you are applying in your resume or CV. To ensure an efficient and fair recruitment process, please refrain from adding a photo in your CV

We commit to an inclusive recruitment process and equality of opportunity for all our job applicants. At [xxxxx] 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.