stillingsbetegnelse:
Validation and Equipment Qualification Responsible

jobbeskrivelse:
•Logistics •Denmark - Bagsværd Would you like to play a key role in the quality of Novo Nordisk’s products and compliance with regulatory requirements? Are you interested in leaving your mark on the validation of our cold chain distribution? Then seize the opportunity to become our validation responsible in Shipping and Customer service. About the department You can look forward to joining a challenging and developing environment with highly competent and dedicated colleagues in Supply Chain Planning. Supply Chain planning’s mission is to ensure aligned, transparent, and efficient supply chain planning from supplier to customer. Specifically, you will a part of the Shipping & Customer Service department, which handles shipping of finished products and raw materials. 37 dedicated colleagues ensure fast and reliable global import/export of Novo Nordisk’s products to our affiliates and direct customers around the world in the right quality and at competitive prices. The job As Validation responsible, you perform transport process validation, e.g. ensuring quality and compliance when transporting Novo Nordisk’s products in a very challenging and unforeseeable environment. In particular, it is your responsibility to make protocols, coordinating tests and document in reports that the products stay within the specific standards of tolerance from the moment they leave the ramp at Novo Nordisk until they reach the final destination somewhere in the world. Together with the carriers and other suppliers, you have the responsibility for documenting equipment qualification and its compliance with the regulation e.g. EU GDP and local legal requirements. Additionally, you produce validation documentation within shipping that supports strategic new product registration in various countries. You also play a key role in preparing and presenting validation documents for Danish and international authorities, and you participate in the audits and inspections, giving a detailed account of the validation methods and the results. The position offers you a unique opportunity to take on an independent job, where you can leave your mark on the department while realising your goals and seeing the benefits of your work in global environment. Qualifications You have combined your Master’s degree in engineering, Pharmacy or another relevant educational background with 5+ years of experience from a similar position within quality or process support. You have a proven track record in GMP and risk analysis expertise and have successfully worked with validation. In everything you do, you are driven by your strong personal commitment and sense of responsibility and you are not afraid to stand your ground when needed. You have a systematic, analytical and thorough approach to your work and you are keen on finding sustainable solutions. You have a sense of initiative and enjoy an independent role where you work as the go-to-person who possesses solid in-depth expertise within your field of work. This job also requires excellent communication and cooperation skills, as you navigate your way around colleagues, foreign authorities and other stakeholders, and balance support and continuous follow-up. Finally, you take pride in meeting your deadlines and you never compromise on quality in your work. 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 call Christina Grauballe on + 45 3075 2053. Deadline 13 July 2014

Arbejdsgiver Navn: NOVO NORDISK A/S

Arbejdsgiver telefonnummer: 44448888

Arbejdsgiver faxnummer: 44442314

land: Danmark

region: Hovedstaden

Kontrakt varighed: Fast

Kontrakttype: Fuldtid

krævede uddannelse: Ikke angivet

Kilde til jobtilbud: AMS, Offentlige arbejdsformidlinger, Danmark