Department Quality Partner
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Måløv
Department Quality Partner Are you looking for a new energetic team where you can transform your GMP and Quality knowledge into training and coaching and where you can unfold your excellent communications skills? And do you have a background in pharma with a strong sense of good quality? If yes, then you might be the one we are looking for to join our ambitious and fast-growing new department! About the department Oral Finished Products (OFP) is organizationally located in Product Supply and is steadily growing to support the demands of the market. We are approx. 850 committed colleagues in ODFP Production in Måløv split between two buildings and we have great ambitions for the future! In OFP, we have set ourselves the ambitious goal of being the first on the market with a tablet containing a GLP-1 based drug. With this ground-breaking tablet we can finally offer patients with type 2 diabetes an alternative to the injectable preparations. This is the ambition we are supporting! Rybelsus 2G is the department responsible for the qualification, ramp-up and production of our new 2nd Generation Rybelsus tablet as well as the production platform supporting several of our future products. We already have approx. 45 employees onboard and we are driven by a patient-focused purpose with an engaging and warm work environment where we welcome new competencies and personalities. The Job We are constantly striving for the highest quality possible with the right touch of necessary and sufficient – and this is where we need you! With the growth of the department and new employees and equipment coming onboard we need a strong Quality partner to support the leaders and the employees in our journey for success: You will be responsible for building and driving our deviation structure to ensure timely follow-up and strong root cause investigation and transparency to deviating issues and corrective actions You will be interacting daily with all employees in the department (operators, skilled workers, and academics) and will support them with quality training, GMP understanding and coaching. You are expected to be the primary driver in ensuring that we can obtain, and sustain, a deeply integrated quality culture in the department and continuously improve our quality mindset. This includes idea generation, planning, implementation, and process confirmation. You will work particularly close with the management team to support, challenge and coach us towards next level and guide us in where in the organization we should direct our quality focus. We will also need you in our daily KPI- and data tracking as well as during quality investigations and trend reporting. Likewise, you will collaborate closely with QA, QMS and Quality Partners in our sister departments as well as support our site setup during audits and inspections. Your Qualifications You have an educational background within health, natural science or similar, and more importantly, you have a minimum of 2 years’ experience from the pharma industry within GMP and Quality requirements. Your experience has taught you how to transfer you own passion for quality and GMP in an involving and respectful manner to motivate colleagues to deliver their best in a dynamic environment. High quality is a trademark for you, and you naturally utilize LEAN in your way of working. You are a trustworthy and good communicator who listens to learn and support as well as set direction to realise your goals and deadlines. Also, you thrive in an environment where change of priorities and new challenges is a part of our daily work and development. Working at Novo Nordisk We are a proud life-science company, and life is our reason to exist. We’re inspired by life in all its forms and shapes, ups and downs, opportunities and challenges. For employees at Novo Nordisk, life means many things – from the building blocks of life that form the basis of ground-breaking scientific research, to our rich personal lives that motivate and energise us to perform our best at work. Ultimately, life is why we’re all here - to ensure that people can lead a life independent of chronic disease. Contact For questions about the position, please contact Director Nanna Mandøe Sverrild +45 34 48 15 37 Deadline September 27th, 2023 Interviews will be conducted on a continuous basis, so don’t hesitate to apply if you are a match to the position. 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 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 Måløv.
Jobbet er oprettet på vores service den 4.9.2023, 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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