QA professionals for Quality Control and Analytical Development

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Gentofte

Are you keen on playing a crucial role in ensuring the quality of products and driving change in Biotech and Rare Disease (BRD)? Do you thrive in a job with lots of professional stakeholder management and professional sparring with colleagues? Would you like to become a member of a highly skilled QA department at the forefront of new products and digitalization? Then you might be our new colleague in BRD QA. The Position As QA, our key task is to ensure products of the highest quality to serve our patients. It is crucial that the products are filed, produced, analysed, and released in full compliance with current practice and guidelines from authorities. The working assignments are versatile and cover the review and approval of several types of GMP documentation, oversight of quality processes through presence in the laboratories and setting direction on quality issues. The QA for QC working assignments are centred around documents related to analytical methods and laboratory equipment. The analyses performed are e.g., HPLC, Bio- and Immunoassay and general pharmacopeia methods including microbiology. In addition, the team also supports development of analytical- and microbial methods for the new products entering our BRD pipeline both in-house and at our Contract Manufacturing Organizations. The team is supporting and overseeing quality activities in BRD QC laboratories in Gentofte, Hillerød and Kalundborg. When joining our department, you will undergo a structured and individual training program, and you can expect increasingly more responsibility. You will have an individual development plan to ensure continuous development and realization of your full potential. We have a high focus on a great work-life balance, with the flexibility to work from the office and home. Qualifications You hold a master’s degree within pharmacy, chemistry, microbiology, or similar. Preferably your academic background is supplemented with experience from the pharmaceutical industry, however we would also like to hear from talented newly academic graduates. In addition,
  • You take responsibility, work independently, and make decisions that balance quality demands, authority expectations, and business needs.
  • You are flexible and have a strong quality mind-set combined with the ability to increase simplicity.
  • You meet your deadlines, and you know how to prioritise between different tasks in an everchanging environment.
  • You have a flair for communication, and you know how to communicate clearly in a good tone, even when the message is not easy.
  • Have good coordinating- and collaboration skills when handling cases with both colleagues and stakeholders.
  • You have a curious, innovative, and solution-oriented approach to overcoming challenges.
  • We expect you to value good workplace relationships and contribute positively to a good working environment.
    • Finally, we operate in an international company, thus the position requires language proficiency in both English and Danish. About the Department You will become a part of the department “BRD QA QC, MDev & Support”, which is a dynamic and well-functioning department with many interfaces and stakeholders around the organization. The department counts 33 employees and consists of three teams. The teams are supporting and overseeing QC laboratories and analytical methods, support functions to production and product life cycle and are highly involved in the core of quality processes and authority inspections. We drive and participate in process expert groups across NN and have a seat in several product core groups, supporting products through the entire lifecycle. The department is an integrated part of projects concerning digitalization, innovation, and automation, providing the opportunity to impact the future state of the organisation. We are currently looking for a new colleague in the QA for QC team. As a QA professional, you will join a group of highly skilled and experienced colleagues. The teams have a high level of self-governance and the working relations are informal. We value good humour and an open and honest culture. We appreciate a colleague who takes responsibility, has a positive and curious approach to new challenges and contributes to a pleasant working atmosphere
    Contact If you want to know more about the position, please contact Associate Manager Anne Dam Poulstrup +45 3075 0343. Deadline Deadline March 12, 2023. NB! Feel free to submit your application in Danish or English. Please note that applications will be reviewed continuously, and interviews will be planned as soon as suitable candidates have been identified. 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.


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

    Arbejdsstedet er beliggende i Gentofte.

    Jobbet er oprettet på vores service den 14.2.2023, men kan have været deaktiveret og genaktiveret igen.

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