Quality Officer

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Are you a pharmacist or similar and have experience with scientific data, working in a GxP (especially GDP) regulated area and/or quality management systems? Do you have an analytical personality with strong attention to details and a "can-do" mentality? And do you want to be part of a great team, in a rapidly expanding organisation close to the market and our customers? If yes, then we have an exciting job opportunity for you as Quality Officer in Novo Nordisk Denmark where you will help us make a difference for patients living with chronic diseases.
Don’t hesitate, apply now! The Position As Quality Officer, you will be part of the Legal, Compliance & Quality (LCQ) team dedicated to safeguarding Novo Nordisk’s license to operate. Your main task will be to help our Quality Manager in driving the Danish affiliate’s quality focus and compliance. You will be a key stakeholder for your colleagues in Denmark and Iceland regarding quality processes, training, documentation, and improvements for Novo Nordisk’s quality management system. At Novo Nordisk, we never compromise on quality and business ethics. Your main goal as Quality Officer will be to help ensure that we locally work in accordance with this statement through quality management to safeguard patients, our products and securing our licence to operate. As a Quality Officer, your primary responsibilities will include:
  • Contribute to the administration of the quality management system by handling tasks such as document control, change control, and deviation handling.
  • Support the assignment of GxP training to new employees, ensuring timely completion of training, and overseeing both annual and ad hoc training sessions within GxP and related areas.
  • Assist the Quality Manager/Responsible Person in inspections, internal audits, and facilitating the Quality Management Review.
  • Ensure adherence to and implementation of EU GDP and local GDP regulations, including compliance with the Danish Medicines Act (Lægemiddelloven).
  • Collaborate with the Quality Manager/Responsible Person to coordinate potential and actual recalls, identifying and mitigating quality risks through innovative solutions.
  • The main workplace will be at our office, with some flexibility to work from home. Our office is located in Ørestaden, Copenhagen. Qualifications
    The candidate possesses a strong quality mindset, analytical and detail-oriented skills, effective stakeholder management and communication skills, confidence in handling complex tasks, an open and solution-oriented mindset, the ability to work both independently and collaboratively, excellent coordination and time management skills, an interest in understanding Novo Nordisk’s business environment, and a proactive approach in identifying challenges and pursuing innovative solutions, demonstrating good judgment in selecting simplified methods for stakeholders.

    In addition, you have:
  • Academic degree, preferably in pharmacy or a related field, or relevant Master of Science degree
  • Knowledge of GxP regulation and industry standards (Danish Medicines Act, EU GDP)
  • Experience in quality management within the pharmaceutical industry is an advantage but not mandatory
  • Interest in learning and operating multiple IT systems within the Quality Management System
  • Fluent English language skills (written and spoken). Some Danish skills are needed, but fluent Danish language skills are not a requirement
  • About the Department Our Danish and Icelandic affiliate consists of approx. 170 employees across sales, marketing, clinical development centre (CDC DK), medical and other functions. With us, you become part of an engaging and dedicated affiliate that strives for excellence. You share our passion and commitment to make a difference to change patients’ lives. As Quality Officer, you will be a part of the relatively newly established Legal, Compliance & Quality team consisting of five people – the LCQ Director, two Legal & Compliance Managers, one Quality Manager and a LCQ Student Assistant, and you will report directly to the LCQ Director.
    Working at Novo Nordisk At Novo Nordisk, we don’t wait for change. We drive change. 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. Working at Novo Nordisk is working toward something bigger than ourselves, and it’s a collective effort. Novo Nordisk relies on the joint potential and collaboration of its more than 60,000 employees to change the lives for the better for millions of patients living with diabetes and other chronic diseases. Together, we go further. Together, we’re life changing. Contact If you have questions, please contact our Legal, Compliance & Quality Director Christian Bennet Rosenbæk, [email protected] (+45 30 79 94 82). Deadline Please, apply no later than 28 January 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.


    Information og data

    Denne ledige stilling har jobtypen "Øvrige", og befinder sig i kategorien "Øvrige stillinger".

    Arbejdsstedet er beliggende i Ørestad.

    Jobbet er oprettet på vores service den 12.1.2024, 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.
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