stillingsbetegnelse: Sr 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. Do you see yourself contributing to high quality and compliance of products used for Novo Nordisk clinical trials globally? About the department You will be part of a dedicated department of 20 colleges located in Måløv. We are part of the CMC Quality Assurance organization, which is responsible for all QA activities related to Investigational Medicinal Products used for the increasing number of Novo Nordisk clinical trials globally. We are looking for a new college to support the quality activities in the clinical supplies part of the Novo Nordisk R&D organisation. The job The organisations continuing high level of compliance, audit and inspection readiness is on top of your agenda. As a Qualified Persons delegate you will certify final packed product for use in clinical trials world wide. You will be responsible for quality assurance of activities and documents related to the labelling, packaging and supplying of product for Novo Nordisk trials globally. You will review and approve procedures, change requests and cases of non-conformities and customer complaints. You will provide quality support to our internal stakeholders where your ability to apply Novo Nordisk and authority regulations and requirements is key to solving challenges in both daily operation and long term development of the business and its quality system. You will interact with colleges across the CMC Supply organisation and also with colleges from other parts of Novo Nordisk A/S both in Denmark but also with affiliates world wide. You can look forward to entering into an energetic and positive working environment where cooperation amongst highly engaged and dedicated Novo Nordisk colleges is key to your and the company’s succes. Qualifications Your approach to this position is a master’s degree as a Pharmacist. The preferred candidate has several years of experience working according to GMP requirements (production/QA) in a pharmaceutical business with a manufacturing authorization from DHMA (§39). Direct experience with GMP work related to clinical trials should be highlighted in your application as this will be weighted highly when evaluating applicants. On a personal level, you demonstrate engagement, credibility and empowerment. You are a positive and open minded team player who can co-operate at all organizational levels. You like a professional and dynamic environment with many simultaneous tasks and changing priorities. You are a skilled communicator, and you thrive on unfolding your high level of energy and spirit in an international, dynamic environment. Feel free to submit your job application in either English or Danish, whichever you prefer. Also please share this add with friends and professional connections you might think would be interested in pursuing a career opportunity at Novo Nordisk. At Novo Nordisk it is your skills, your commitment and your ambitions, which helps us to improve many people's lives. In return we offer you the opportunity to work with exceptionally talented colleagues, and we offer you a wide range of opportunities for professional and personal development. Contact For further information, please call Birthe Boldvig Rottwitt on +45 3075 0158. Deadline 20 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