Arbejde Senior QA Project Manager in CMC Development Hovedstaden Novo Nordisk A/S - jobtilbud

GÆLDER
stillingsbetegnelse: Senior QA Project Manager in CMC Development

jobbeskrivelse:
- Quality - Denmark - Bagsværd Are you interested in working with quality of new products? Do you want to be part of cross collaborational project teams in R&D? Then you could be the new QA project manager we are looking for. About the department Chemistry, Manufacturing and Control (CMC) project planning and management QA is a unit in the CMC Development QA organisation, belonging to R&D. We have the responsibility for project management of CMC quality assurance activities for the entire Novo Nordisk portfolio of development projects. We are managing projects from early development to launch, ensuring optimal collaboration across CMC Development QA as well as with Product Supply QA. We are 13 highly skilled and dedicated employees including 11 QA project managers. Our mission is to act as one point of entry for R&D projects to the quality organisation. The position Your main tasks are to ensure the quality in a number of product development projects and to coordinate QA activities. You will be our representative in the CMC Development Core Group, where you will work closely with the CMC project manager in order to ensure progress and the right level of quality. You will act as advisor to the projects in all quality matters, and be the driver of solving quality issues. You will make sure that quality activities are planned and fulfilled according to company policies. You will support the entire product development process and interact with all areas involved in development of new product candidates. You will establish and lead relevant QA groups consisting of professionals performing QA activities. You will also be involved in collaborations with contract manufacturing organisations. Improvement tools such as LEAN and quality risk management will be part of your daily work. Qualifications You hold a MSc or PhD in Pharmacy, Engineering, Biology, Chemistry or similar and have thorough work experience with GMP, preferably from a QA organisation. You have experience with project management, and a solid background within pharmaceutical development and/or pharmaceutical production. Excellent English skills are a prerequisite. We expect you to have a strong quality mind-set as well as excellent communication and stakeholder management skills. You adapt easily to a changing environment and new priorities. You have a well-structured approach to your tasks and are capable of maintaining an overview, also when under pressure. You have a high sense of responsibility, you can work independently, and show initiative. You never lose focus, despite changing demands or tight deadlines. For more information please see link: http://www.novonordisk.com/cmc-careers 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 Kirsten Schultz at +45 3079 4602 or Johan Söderqvist, +45 3075 6239. Deadline 7 August 2016.

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

GÆLDER

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