Senior QA Professional, Emerging Technologies QA for Manufacturing Development
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Are you passionate to set direction within emerging technologies and to ensure compliance? Are you skilled in navigating complex stakeholder landscapes and motivating teams to deliver great results? Do you thrive in a constantly changing environment with various challenges and growth opportunities to handle? If so, we have an exciting opportunity for you within Emerging Technologies QA for Manufacturing Development. Apply now and become a valuable member of Novo Nordisk - a worldwide pharmaceutical industry leader! The Position As a Senior QA Professional in our Emerging Technologies QA team for Manufacturing Development, you will play a critical role in ensuring the quality and compliance of our novel manufacturing methods, products, and technologies. Your responsibilities will include: Review and approve documents related to stability, process validations, and product specifications for oral drug products and active pharmaceutical ingredient products Lead complex cases with a high level of attention Drive innovation and digitalization projects with stakeholders both locally and internationally Help set the quality direction and ensure alignment across the organization Focus on influencing and setting the right level of compliance, optimizing processes through a LEAN mindset, and establishing new processes that support our business objectives Given the growth we are experiencing in the oral platform and small molecules, a diverse set of competencies are required to strengthen our team, and we are open to welcoming experienced candidates at different levels of seniority for this role. Therefore, this role will be adjustable depending on the right candidates. If you are a self-motivated and detail-oriented professional with a passion for quality, we encourage you to apply for this exciting opportunity. Qualifications An ideal candidate is expected to have: MSc in Pharmacy, Engineering, Biology, Chemistry or similar Solid experience within the pharmaceutical industry, and a minimum of +7 years of experience with quality assurance and/or production. However, as we have more positions, we have the possibility to shape the position according to experience, so please do not hesitate to apply with less experience Experience with both small molecules and API/solid dosage forms (tablets) in a GMP environment will be an advantage Contract manufacturing organisation experience will also be considered a plus Profound understanding of the important aspects of regulations, requirements and guidelines for pharmaceutical development and production The most important asset that you can bring to succeed in this job is a well-developed understanding of quality and a natural urge to handle quality issues at the right level, make decisions and follow-up on quality related problems. On a personal level, you need to have strong communication and interpersonal skills as we highly value the ability to collaborate effectively within a team while also having the courage to question the status quo. We seek a self-motivated, responsible, and proactive individual who can efficiently manage multiple tasks, thrive in a dynamic work environment where teamwork is paramount, and enjoys engaging with a diverse range of stakeholders, both within and outside the organization. About the department You will become part of a great QA department (QA Department for Manufacturing Development, Support and Quality Control), with many interfaces around the organisation. The department consists of around 30 people divided into three teams, and this position is in the QA for Manufacturing Development team. The team consists of 6 highly knowledgeable and skilled people, covering the diverse area of Manufacturing Development. In the department, we take great pride in our work and value challenges as opportunities. We have a vibrant and positive working environment, good values and exchange of knowledge and experience. We all work towards continuously improving our competences, as well as making work processes more efficient and effective. You will be part of Emerging Technologies (ET), that aim to receive and mature emerging technology platforms coming from our internal pipeline as well as from external acquisitions. Our vision is to pioneer the future by maturing and operating emerging technologies in a sustainable way to serve patients with high quality and life changing products. We are guided by our vision and live our culture every day to change lives for our patients. Working at Novo Nordisk At Novo Nordisk, 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 Maja Gro Rydahl (Associate Manager) at +45 3448 5519. Deadline Deadline to apply for this position is 26 November 2023. Applications will be evaluated continuously when received, and candidates may be called for interview before the deadline. 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.
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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 29.9.2023, 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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