Quality Assurance Specialist for Manufacturing Science and Technologies

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Are you passionate about ensuring compliance? Looking forward to put to use your expertise within small molecules, stability, and lifecycle management? Do you thrive in navigating complex stakeholder landscapes and motivating teams to deliver great results? If so, we have an exciting opportunity for you, read more below and apply!
The position
In the role of QA Specialist within our Emerging Technologies QA for Manufacturing Science and Technologies (MSAT), you will play a pivotal role in maintaining the optimal compliance level. Your expertise will be sought in complex compliance cases, where you will provide scientific direction and collaborate with your leader to advance the team's scientific capabilities. Your core responsibilities will include:
  • Serving as a QA specialist for manufacturing science and technologies

  • Taking responsibility and participate as QA for MSAT in the related Novo Nordisk Process Groups

  • Acting as a sparring partner for stakeholders when it comes to QA for new groundbreaking technologies, providing technical expertise and guidance on quality-related issues

  • Ensuring the quality and compliance of our novel manufacturing methods, products, and technologies.

  • Moreover, you will be a main actor in fulfilling the QA strategies and being QA responsible in future strategic initiatives. You will continuously participate in other cross-functional activities to support the development and optimization of manufacturing processes and the implementation of new technologies and analytical methods to improve product quality and efficiency.
    We take pride in assuring that you always have challenging and impactful working assignments to ensure continuous development and realization of your full potential. Equally important, we have a high focus on a great work-life balance, with the flexibility to work from the office and home. This position will be situated in Taastrup from September 2024, and the office presence is expected at minimum three days weekly. Qualifications We are looking for a candidate with a profound comprehension of quality principles and an instinctive drive to address quality issues effectively. You should be confident and adept at navigating the delicate balance between quality requirements, regulatory expectations, and business objectives. To succeed in this role, you:
  • Hold a master’s degree in Biology, Engineering, Pharmacy, Chemistry or similar

  • Have extensive experience quality assurance and/or manufacturing and development

  • Have gained said experience in either the pharmaceutical or medical devices industry

  • Have excellent stakeholder management skills, even in addressing complex matters and tough decisions

  • Are fully proficient in English

  • In depth knowledge about stability and specifications of small molecules and API/solid dosage forms (tablets) will be seen as an advantage. On a personal level, you are proactive, self-driven and demonstrate a high degree of responsibility and initiative, with the ability to prioritize tasks effectively. You thrive in a dynamic setting that values teamwork and are skilled at engaging with a diverse range of stakeholders, both internally and externally. Finally, you are committed to achieving objectives in line with strategic plans, they will focus intently on delivering results and adhering to deadlines.
    About The Department Emerging Technologies QA is a new area within Novo Nordisk where the oral portfolio plays a significant role, currently employing approximately 100 employees but still growing. We work with assuring quality and compliance of the facilities, the equipment, QC lab, manufacturing development as well the release of tablets and future emerging technologies products for the market. We are proud to work in a fast-growing part of Novo Nordisk. You will become part of a great QA department (Emerging Technologies QA New Entry & Support), with many interfaces around the organization. The department consists of around 30 people divided into four teams, and this position is in the QA for Manufacturing Development team. The team consists of 9 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.

    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 QA Manager Maja Rydahl at +45 3448 5519.

    Deadline
    21 July 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 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 5.7.2024, 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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