QA Professional for CMC API Facilities

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  • Quality
  • Bagsværd

Do you want to use your strong quality mind-set and great interpersonal skills to make a difference within QA? Are you eager to play an important role in ensuring the quality and safety of products for clinical trials? If so, then this position as QA Professional can be a unique possibility for you.

As part of Novo Nordisk’s R&D family, CMC Development makes a difference for patients with chronic diseases across the world and the organisation develop, manufacture and distribute drug candidates for non-clinical and clinical trials.

CMC Development and CMC QA is an ambitious organisation with a strong culture, that always seek to solve problems, have an eye for the entire business and do our best to deliver despite any obstacles along the way. We have a high focus on delivering high quality to our customers which is why we are looking for a QA Professional to take an active part in securing our quality level.

About the department

CMC API QA has a mission to assure each and every Active Pharmaceutical Ingredient (API) activity in our development projects live up to the cGMP requirements for the safety of our patients. In CMC API QA we are 25 colleagues divided into two teams. You will be part of a dedicated team of 10 highly qualified technicians and professionals that ensures qualification of facilities and equipment and status assignment of products in Downstream Facilities in CMC API.

The job

As a QA Professional, you will be responsible for delivering best-in-class quality of qualification of facilities and equipment used for GMP production of the API for clinical studies. You will collaborate cross functional with scientists in the pilot downstream production and your QA colleagues.

In your daily work you will challenge and approve documentation regarding qualification of facilities and equipment and other supporting documents also from Contract Manufacturing Organisation (CMO). You will evaluate requirements and set the quality direction for the pilot downstream production and projects.

In our department, we are continuously improving the quality of work, and we are constantly optimising our methods and processes to increase simplicity across CMC QA and CMC Development. We make a difference in the lives of people participating in clinical trials in Novo Nordisk A/S, by ensuring that the products they receive are safe, of the highest quality, and produced in compliance with legislation.

Qualifications

You hold an MSc in Pharmacy, Engineering, Biology, Chemistry or similar. Experience within a GMP and LEAN focused environment is an advantage combined with understanding of how the pharmaceutical industry works.

The most important asset 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.

You are a person interested in building sound relations with your broad stakeholder network. You like to go out and meet your stakeholders and proactive bring QA in action within the organisation. Furthermore, you are a self-driven and independent person with a high sense of responsibility and initiative.

You thrive in a dynamic environment, where teamwork is on the top of the agenda, and like working with many different stakeholders.

As we operate both in a national and an international environment, you must speak and write Danish and English fluently.

Contact

For further information, please contact Rikke Wissing Jensen at +45 3075 1566.

Deadline
10 January 2020.

Millions rely on us
To work for Novo Nordisk you will need the skills, dedication and ambition to change lives for the better for millions of patients living with diabetes and other chronical diseases. In exchange, we offer the chance to be part of a truly global workplace, where passion and engagement are met with opportunities for professional and personal development.


Information og data

Denne ledige stilling har jobtypen "Forretningsudvikler", og befinder sig i kategorien "Kommunikation, marketing, salg".

Arbejdsstedet er beliggende i Bagsværd.

Jobbet er oprettet på vores service den 17.12.2019, men kan have været deaktiveret og genaktiveret igen.

Rapportér
Dagligt opdateret: Dette job opdateres dagligt ud fra jobudbyderens hjemmeside via vores søgemaskineteknologi og er aktivt lige nu.
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