Quality Coordinator
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Are you passionate about ensuring quality standards and processes? Do you thrive in a dynamic and evolving environment? We are looking for a Quality Coordinator to join our team in Chemistry, Manufacturing and Control (CMC) Shipping at Novo Nordisk. If this sounds like a position just for you, apply now and join our team! The position
As our new Quality Coordinator you will collaborate with others in order to develop and maintain the Quality Management System. You will work closely together with team colleagues, QA, and internal and external stakeholders where you will use both GMP and GDP requirements as guiding principles in decisions to find solutions for activities related to moving clinical trial materials across the world. This will ensure that sufficient knowledge safeguards patients when discovering and developing new pharmaceuticals. The main tasks will be to:
• Update and maintain Standard Operating Procedures (SOPs), templates, and guidelines.
• Perform internal reviews of shipping documents and handle deviations.
• Contribute to an inspection-ready culture and ensure compliance with regulatory requirements.
• Oversee and support shipping activities for both GMP and non-GMP materials used in clinical trials.
• Coordinate shipments to get hands-on process understanding. Qualifications
To be successful in this role, you:
• Hold a MSc in Pharmacy, Supply Chain Management, Biology, Chemistry, or another relevant discipline.
• Have 1-2 years of work experience from Quality Assurance/Quality Management System/Project Management/GMP or/ and Pharmaceutical industry.
• Are fluent in English and preferably also in Danish. The most important asset that you can bring to succeed in this job is a well-developed understanding of quality and a natural sense for structure and detail. You take a systematic approach to problem solving and have a strong quality mindset. As a person, you see yourself as being self-motivated, can work independently, proactive and can work systematically to strive for simplicity in processes. It is crucial for us that our new employee is an empathic team-player and is thriving in a dynamic work environment. About the Department As part of Product Supply, Quality & IT (PSQIT) organisation, Chemistry, Manufacturing and Control (CMC) Development & Scaling makes a real difference for patients with chronic diseases across the world. We develop, manufacture and distribute drug candidates for clinical trials and have a strong culture with a “can do” mind-set.
The CMC Shipping team is part of the CMC Active Pharmaceutical Ingredients (API) Process Operations department, anchored in CMC API development. CMC API Process Operations plays a key role in securing the patient safety in the clinical trials from the entire development portfolio. Your new team consists of 9 dedicated, knowledgeable, fun, and open-minded full-time employees, located in Søborg. We value social interaction and offer a supportive and collaborative work environment. While the position is office-based, we also offer flexibility to work from home when appropriate.
Working at
At , we don’t wait for change. We drive it. We’re 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 embrace 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, through to manufacturing, marketing and sales – we’re all working to move the needle on patient care.
Contact
For further information, please contact associate Manager, Marit Klette at +.
Deadline
Apply before June, 9 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 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.
As our new Quality Coordinator you will collaborate with others in order to develop and maintain the Quality Management System. You will work closely together with team colleagues, QA, and internal and external stakeholders where you will use both GMP and GDP requirements as guiding principles in decisions to find solutions for activities related to moving clinical trial materials across the world. This will ensure that sufficient knowledge safeguards patients when discovering and developing new pharmaceuticals. The main tasks will be to:
• Update and maintain Standard Operating Procedures (SOPs), templates, and guidelines.
• Perform internal reviews of shipping documents and handle deviations.
• Contribute to an inspection-ready culture and ensure compliance with regulatory requirements.
• Oversee and support shipping activities for both GMP and non-GMP materials used in clinical trials.
• Coordinate shipments to get hands-on process understanding. Qualifications
To be successful in this role, you:
• Hold a MSc in Pharmacy, Supply Chain Management, Biology, Chemistry, or another relevant discipline.
• Have 1-2 years of work experience from Quality Assurance/Quality Management System/Project Management/GMP or/ and Pharmaceutical industry.
• Are fluent in English and preferably also in Danish. The most important asset that you can bring to succeed in this job is a well-developed understanding of quality and a natural sense for structure and detail. You take a systematic approach to problem solving and have a strong quality mindset. As a person, you see yourself as being self-motivated, can work independently, proactive and can work systematically to strive for simplicity in processes. It is crucial for us that our new employee is an empathic team-player and is thriving in a dynamic work environment. About the Department As part of Product Supply, Quality & IT (PSQIT) organisation, Chemistry, Manufacturing and Control (CMC) Development & Scaling makes a real difference for patients with chronic diseases across the world. We develop, manufacture and distribute drug candidates for clinical trials and have a strong culture with a “can do” mind-set.
The CMC Shipping team is part of the CMC Active Pharmaceutical Ingredients (API) Process Operations department, anchored in CMC API development. CMC API Process Operations plays a key role in securing the patient safety in the clinical trials from the entire development portfolio. Your new team consists of 9 dedicated, knowledgeable, fun, and open-minded full-time employees, located in Søborg. We value social interaction and offer a supportive and collaborative work environment. While the position is office-based, we also offer flexibility to work from home when appropriate.
Working at
At , we don’t wait for change. We drive it. We’re 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 embrace 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, through to manufacturing, marketing and sales – we’re all working to move the needle on patient care.
Contact
For further information, please contact associate Manager, Marit Klette at +.
Deadline
Apply before June, 9 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 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.
Information og data
Denne ledige stilling har jobtypen "Øvrige", og befinder sig i kategorien "Øvrige stillinger".
Arbejdsstedet er beliggende i Søborg.
Jobbet er oprettet på vores service den 27.5.2024, men kan have været deaktiveret og genaktiveret igen.
Dagligt opdateret: Dette job opdateres dagligt ud fra jobudbyderens hjemmeside via vores søgemaskineteknologi og er aktivt lige nu.
- Øvrige
- Søborg
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