stillingsbetegnelse: GMP Material Expert

jobbeskrivelse:
- Sourcing - Denmark - Bagsværd Are you looking for an opportunity to apply your knowledge about and experience within GxP requirements, quality and compliance for Raw materials? Do you enjoy setting up and optimizing processes in interaction with many stakeholders? Then you may be the new GMP Material Professional in Sourcing Operations (SoOp) in Bagsværd. About the department You will join Sourcing Operations; a dynamic area responsible for purchasing, warehousing and quality control of raw material, primary packaging material and printed packaging material for production and clinical trials. You will be a part of the new department Raw Material Manufacturing Development, which is responsible for ensuring effective transfer of materials from development projects to Product Supply, and for managing control strategies for all GMP materials. The department collaborates intensively with all parts of Sourcing Operations, Strategic Sourcing, CMC, QA and ManDevs to strengthen Novo Nordisk through global supply of quality materials. The job As GMP Material Professional you will be a key person in transferring Raw materials from development projects to production. You will support the processes related to establishment, update, maintenance and discontinuation of GMP Materials, and thus have a high degree of interaction with Material Responsible colleagues throughout Novo Nordisk. You will own the GMP Material Control Strategies, and thus drive risk assessments and the development and maintenance of the control strategies themselves. In this sense you will In your daily work you will have a high degree of interaction with stakeholders from throughout CMC and Product Supply, while working focused on establishing a structured and transparent setup for control strategies and transfer of materials. The position as GMP Material Responsible is newly established and you will therefore play a pivotal role in setting up and use your knowledge of regulatory requirements to GMP materials to ensure that control strategies takes supply chain concerns into consideration while always being compliant to regulatory requirements. defining the role in SoOp. Qualifications You hold a relevant academic degree (e.g. Pharmacy, Chemical engineering or Chemistry) and have extensive experience from working within the pharmaceutical industry with GMP, quality and compliance requirements, preferably in regards to GMP materials used for manufacturing of drug substances and drug products. You work structured and systematic, and have strong coordination, communication and networking skills. Lastly, you are proficient both in spoken and written English. 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 Mette Ingrid Langkjær at +45 3075 9782 or Malene Gundestrup at +45 3075 9703. Deadline 10 May 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