stillingsbetegnelse: QA Professional

jobbeskrivelse:
- Quality - Denmark - Måløv Our growth is your opportunity Being part of Novo Nordisk Research & Development means working at one of the world's largest and most successful biopharmaceutical companies. Our R&D organisation is vital to Novo Nordisk's continued growth and we always welcome talented people who would like to grow with us. We are expanding in CMC Analysis QA within R&D, Novo Nordisk A/S. Therefore, we are seeking two new colleagues with drive and personality. Would you enjoy the high activity of the QA work within a pharmaceutical development environment? Then you might be the QA Professional with the drive and performance we need. About the department In CMC Analysis QA you will be working with 12 highly dedicated colleagues to assure that all our analysis development processes and development laboratories meet the internal and external requirements. The job In close cooperation with your colleagues, you act as a consultant for our analytical development departments. You contribute to find solutions for ad hoc questions and challenges within compliance of the analytical development activities. You will approve qualification and validation documentation from analytical departments in the process of release of Active Pharmaceutical Ingredients (API) and Drug Product (DP) for clinical trials. You have a risk based approach to the development process and product, and you contribute to find the right balance between patient safety, compliance to requirements and effective business conduct. CMC Supply’s continuing high level of audit and inspection readiness is on top on your agenda. In CMC Supply QA we work with QA oversight where you proactively together with your colleagues will identify areas where our stakeholders’ compliance can be strengthened. Qualifications You hold a Master’s degree in Pharmacy or possess equivalent qualifications besides a strong quality mindset. You have experience with GMP, analysis validation, analysis equipment qualification as well as laboratory computer system validation. Qualifications within analytical IT system regulatory requirements will also be regarded as a plus. You are fluent written and spoken Danish and English on a professional level. With your good cooperation and communication skills you are able to organise and drive tasks. You take a pragmatic approach to problem solving and have strong interpersonal skills. You are detail-oriented with a strong quality mind set and are a team player, but also able to work independently. You thrive on working across departments in an international organisation. We look for an open minded person with an outgoing attitude, natural networking skills. And we would enjoy having a straightforward person with a good sense of humour in our department. Working at Novo Nordisk At Novo Nordisk, your skills, dedication and ambition help us change lives for the better. In exchange, we offer you an opportunity to work with extraordinary talent and benefit from a range of possibilities for professional and personal development. Contact For further information, please contact Pernille Uldall Bolvig +45 3079 7548. Deadline 16 February 2015.

Arbejdsgiver Navn: Novo Nordisk A/S

Arbejdsgiver telefonnummer: 44448888

Arbejdsgiver faxnummer: 44442314

Job kort beskrivelse: Farmaceutarbejde

land: Danmark

region: Hovedstaden

Kontrakt varighed: Fast

Kontrakttype: Fuldtid

krævede uddannelse: Ikke angivet

Kilde til jobtilbud: AMS, Offentlige arbejdsformidlinger, Danmark