stillingsbetegnelse: Quality Management System Specialist

jobbeskrivelse:
- Quality - Denmark - Bagsværd Is quality a vital part of your DNA, and do you have the pharmaceutical GMP experience and knowledge to play a key role as focal point within quality systems and processes? If so, we have just the right job for you as Quality Systems Specialist. You will be trusted with major responsibility and the mandate to make decisions within your field of expertise. About the department You will join Aseptic Production Support and Optimisation, DFP Manufacturing Development. We deliver aseptic production support to Diabetes Finished Products. We are approx. 60 skilled and dedicated colleagues covering a wide range of expertise, and we are looking forward to welcoming you to our team. The job You will become our CVP and Director’s right hand within quality systems where you will provide daily support to the department and the area. As such, you will have a challenging and exciting role as combined Quality Group Chairperson in Diabetes Finished Products Manufacturing Development (DFP ManDev) and our local Quality System Specialist within the department. In addition you will become member of our Local Change Group. You will be responsible for our Quality Management Review (QMR) and handle planning, coordination, follow up, trend analysis and reporting. You also define, implement, maintain and promote DFP ManDev’s Quality Management System as well as identifying and mitigating compliance risk’s. Further you will act as CAPA SME for the area and use your expertise to provide training and promote GMP knowledge. Internal and external audits including inspection and follow up will also be part of your responsibility. As local Quality System Specialist you will generally handle the same tasks but at department level. Qualifications You have a Master’s degree in one of the Natural Sciences, Engineering or the like and at least 10 years experience from working in GMP regulated pharmaceutical industry. Today you probably hold a role as Quality Compliance Manager, Quality Compliance Specialist /Senior Professional and you can see the career and development perspectives in joining a world-leader in a truly international setup. Your career has provided you with broad experience within quality systems management; optimisation and product supply processes as well as in depth ISO/GMP knowledge. Your mind is set on structure and compliance, and you never compromise on quality in your work. You are comfortable handling many stakeholders at the same time, and your systematic approach makes it possible. You are used to handling complex tasks and to deliver in due time, and you have a diplomatic and constructive way of communicating your requirements. At Novo Nordisk, you can look forward to change. We encourage our employees to make the most of their talent. And we reward hard work and dedication with the opportunity for continuous learning and personal development. Contact For further information, please call Casper Berg on +45 3075 6241. Deadline 5 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