Associate Manager QA Supporting Functions

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Associate Manager QA Supporting Functions Do you have a high-quality mindset and the ability to set direction, engage and energize your colleagues? Do you want to develop your leadership skills? Are you passionate about improving processes, and raising the bar for delivery while sustaining the high level of quality and compliance? Apply today and join us as associate manager for our new QA team for Supporting Functions at [xxxxx] Pharmatech A/S in Køge. The position We are a fast-growing organisation with an ambitious strategy for new products and new markets where our supporting functions play a key role for us to succeed. The position requires, that you are driven by complex challenges and a broad area of responsibility in a dynamic environment. You play a key role in setting direction, motivating, and developing:
  • The team and each of the individual team members

  • The team towards our stakeholders in [xxxxx] Pharmatech. The stakeholders are Supply Chain, Warehouse, IT, Microanalysis lab, QC lab and Technical Support

    • You will be leading 7-9 experienced and highly qualified professionals. Together with the team you will be responsible for:
  • Ensure that all work performed in QA Supporting Function is compliant to rules and regulations (GMP and compliance, current industry practise and authorities’ expectations)

  • Driving agreed operational plans in the team and/or across QA teams

  • Ensuring resources for and balancing priorities according to overall tasks and deadlines

  • Decision making in relation to quality and planning towards our stakeholders

    • The team handles classic QA tasks such as deviations, CAPAs and change control but is also heavily involved in different project and optimisation processes at [xxxxx] Pharmatech. You are expected to act as a role model demonstrating a strong quality mindset and to support anchoring of our culture in the growing organization. Qualifications To succeed in this role, you have:
  • Experience with people management of highly skilled employees preferably within a GMP regulated pharmaceutical industry

  • A relevant university degree e.g.Pharmacist, Chemical Engineer, Chemist etc.

  • A background from QA, QC, RA, or Production Support

  • An interest in developing your leadership skills

    • As a person, you have an innovative mind-set and the ability to work effectively in a team-oriented setting. Openness, honesty, focus on continuous improvements and quality mindset are natural parts of your personality and the way you work. You have a can-do attitude and focus on opportunities rather than limitations. About the department QA Supporting Functions is a part of the QA & RA department at [xxxxx] Pharmatech. The department currently consists of 29 employees working diligently to support the entire value chain, from Research & Development to Production and finally Sales & Marketing. You will have a close collaboration with the two other managers in the department where we value close collaboration, sharing our successes and challenges and a good laugh. [xxxxx] Pharmatech A/S is a 100% owned subsidiary of [xxxxx], located in Køge. We are more than 400 people covering the entire value chain from R&D and Business Development to Manufacturing, Marketing & Sales. Novo Nordisk Pharmatech A/S is a global and leading manufacturer of pharmaceutical ingredients for the pharmaceutical and biopharmaceutical industries. Our purpose is to enabling better medicines and better lives by providing sustainable pharmaceuticals materials though innovative and customised solutions. Our product range consists of Quaternary ammonium compounds (Quats), Recombinant Insulin, Customised Purification Resins, and Speciality Enzymes. Working at [xxxxx] At [xxxxx] 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, background, 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. Contact For further information, please contact: QA Manager Louise Vilstrup Thøgersen (until July 31st) at +[xxxxx]QA Manager Daniel Grundahl (after July 31st) at +[xxxxx] Deadline 11 August 2024. Applications will be reviewed, and interview conducted on an ongoing basis so you are encouraged to apply as soon as possible. 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 [xxxxx] 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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    Arbejdsstedet er beliggende i Køge.

    Jobbet er oprettet på vores service den 16.7.2024, men kan have været deaktiveret og genaktiveret igen.

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