stillingsbetegnelse: Quality Coordinator

jobbeskrivelse:
- Quality - Denmark - Måløv We are looking for a Quality Coordinator to join our staff team and join us in ensuring quality compliance in our department. You will be responsible for ensuring that quality is always in top of mind across the department. Chemistry, Manufacturing and Control Supply (CMC) is a part of the Research & Development organisation, manufacturing and distributing drug candidates for pre- and clinical trials. We develop and formulate all new protein and peptide processes coming out of our research units in our pilot plants, ensuring that we bring best-in-class treatments to the market. CMC Supply is organised in seven areas of expertise supporting the entire drug development pipeline. Working in CMC Supply, you’ll be part of a team of the best and brightest in your field, where scientific integrity is standard and shared responsibility taken for granted. About the department Clinical Supplies Supply Chain Planning (CSSCP) is a key member of CMC Clinical Supplies (CS) in the R&D organisation. CS is responsible for planning, production, packaging and distribution of products for all clinical trials conducted globally by Novo Nordisk. Supply Chain Planning consists of 40 employees located in Måløv. The department is organised in three teams; Temperature Control & Material Planning, Supply Planning Late Phase and Supply Planning Early Phase & Operations. Our responsibility is to ensure that trial products are available on time and in the right quality and quantity for all clinical trials conducted globally by Novo Nordisk. We operate in the combined field of supply chain management and regulatory requirements within drug development. We are involved from first human dose to phase IV trials. The job By driving the department quality management processes you will be responsible for ensuring the department comply with current quality requirements. Some of the main themes to secure this are setting the right quality goals and implement the right initiatives to reach these goals in collaboration with the management team. You will act as discussion partner to your colleagues and the management team to ensure the department always reach the right quality level. Dialog and training of the employees is also a priority in this job. In some cases you will also be writing the required documentation such as non-conformities, change requests and standard operating procedures. Qualifications The job requires a scientific academic background. It is required for you to have experience working with pharmaceutical production or a quality function in a highly regulated industry. You possess assertiveness and are able to set and communicate goals followed by a structured approach to reach these goals. Collaboration in a broad perspective is a must since both daily dialogue with staff in the teams and broad stakeholder management is required. Working independently must be a part of your preferred working environment. 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 If any further information is needed, please contact Stine Mørch at +45 3079 9847. Deadline 3 August 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