Arbejde Qualification Pilot Scientist for Pilot Plant Production Hovedstaden Novo Nordisk A/S - jobtilbud

GÆLDER
stillingsbetegnelse:
Qualification Pilot Scientist for Pilot Plant Production

jobbeskrivelse:
- Research & Development - Denmark - Måløv Are you eager for being part of Novo Nordisk A/S major quest within tablets? Do you want to influence a department in rapid development? If so you have to apply for this job. About the department We are 35 colleagues, who are organised in two teams and responsible for development and manufacturing of oral protein products for preclinical and clinical trials. The department covers a broad and exciting range of process technologies for solid dosage forms, technical support, and project management and execution related to qualification of equipment, utilities and facility. The Job You will play an absolute key role in our business critical efforts to ensure and maintain the facility’s license to operate. Across your tasks and projects you therefore will have a close collaboration with different team members and other departments in OPF (Oral Protein Formulation), ensuring that our project time lines and deliverables are met. Your primary focus will be challenges related to process optimisation and validation/qualification of facilities and equipment for GMP use. A vital part of your job is to ensure that equipment and facilities are in compliance with cGMP standards. As project validation responsible you also handle updates and optimisation of our equipment procurement flow matrix – from project feasibility start to release for GMP production including, supplier contact, risk analysis, impact assessment, URS, user instruction and DQ, IQ, OQ, and PQ qualification. Qualifications You are educated in engineering, as pharmacist or possess a strong scientific background in your former employments on a high documented high level. Your previous career has provided you with solid experience within qualification/validation of pharmaceutical production equipment, facilities and facility management all within production of solid dosage forms. You have worked with GMP, GAMP and ISO, IT requirements and in this you use your combination of a strong quality mindset, overview and keen eye for details. In addition, you shall have a solid background in computer validation and a good understanding of GAMP methodologies and risk analysis. You thrive on handling multiple tasks simultaneously in a dynamic environment where everyone contributes to the team’s success with a positive attitude to challenges, dedication and a flexible attitude towards creating considerable results. 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 Thilde Bøgebjerg at +45 3075 3165. Deadline 6 January 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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