stillingsbetegnelse:
QA Professional for Release of Tablets for Clinical Trials, CMC OPF QA

jobbeskrivelse:
- Quality - Denmark - Måløv Are you looking for new challenges within QA – development of tablets for clinical trials and do you want to make a difference? The oral project portfolio is reaching clinical phase 3. We are looking for a dedicated, professional and enthusiastic new colleague. About the department In CMC OPF QA we have the responsibility for quality assurance of oral formulations and release of tablets for clinical trials. We have the QA responsibility of the oral formulation development department, the oral pilot production, and building of a new facility for phase 3 production. The job In close cooperation with your 13 colleagues in QA, you act as a consultant for our pilot and formulation departments. You will act as qualified person delegate, and you will have the overview of the process within development and production of tablets. The job is a combination of development project and facility related QA tasks in a complex and changing environment. You will approve documentation for development, manufacturing, stability, and QP release of tablets for clinical trials. You will assure that the development documentation is compliant with internal and external requirements. You will approve facility related documentation needed for the operation of the oral pilot plant. CMC Supply’s continuing high level of audit and inspection readiness is on top on your agenda. In CMC Supply QA we work with QA oversight where you proactive together with your colleagues will identify areas where our stakeholders’ compliance can be strengthened. You have a risk based approach to the development process and product, and you contribute to find the right balance between patient safety, compliance to requirements and effective business conduct. Qualifications Ideally, you have a master in Pharmacy or corresponding qualifications and at least 1-2 years of experience within the pharmaceutical industry. You have thorough knowledge within more of the following areas: experience from tablet manufacturing/development, GMP, validation/qualification, requirements for tablet production, and requirements for investigational medicinal products for use in clinical trials. You enjoy working in a dynamic environment, where teamwork is at the top of the agenda. Also, you are quite adaptable and challenge our way of doing things, so that we will get even better. You focus on results and quality – and contribute to the right level of compliance. 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 Janne Lavritsen +45 3075 7333. Deadline 3 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