Quality Assurance Advisor for AstraZeneca
AstraZeneca / Proffice Link AB / Apotekarjobb / Göteborg
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Mölndal,
Partille,
Kungälv,
Lerum eller i
hela Sverige Visa alla jobb hos AstraZeneca / Proffice Link AB i Göteborg,
Mölndal,
Södertälje,
Stockholm eller i
hela Sverige For AstraZeneca we are now looking for a Quality Assurance Advisor for a consultant assignment starting in March that will go on until December 2017.
Interviews and selections are held on an ongoing basis so please apply today!
Publiceringsdatum2016-02-22Dina arbetsuppgifterPharmaceutical Development's Quality Assurance function is recruiting a Good Manufacturing Practice QA Advisor. The QA Advisor role has a broad range of responsibilities to ensure that activities and processes in Pharmaceutical Development functions and the R&D supply chain comply with Regulatory requirements, GMP and AZ internal quality system requirements.
Interactions occur among various internal functions and sites, but also with vendors and suppliers. The role is based at Mölndal in Sweden.
Your major responsibilities will be:
• Responsible for QA approval of documentation related to manufacturing equipment and facilities to ensure compliance, including maintenance, calibration, validation and change control.
• Support the Pharmaceutical Development functions with investigations of deviations and other quality and compliance decisions
• Interpret, trend and report compliance data, to measure and improve quality standards
• Responsible for conducting internal or external QA/GMP audits
• Developing QA Agreements with suppliers or contractors delivering services or products to the Pharmaceutical Development Supply Chain.
• Provide appropriate QA input to business/quality regulated improvement projects
• Close collaboration with AstraZeneca QA colleagues globally.
Utbildning/erfarenhet
You have a Scientific degree with at least 3 years' experience of working within a pharmaceutical GMP environment, a broad understanding of Quality Systems and GMP and comprehensive understanding of the pharmaceutical/drug development process. You are a good communicator with experience of interacting effectively across interfaces and is fluent in written and spoken English (Swedish is not a requirement). Preferrably you have experience within a pharmaceutical manufacturing organization, good team working and networking skills, capability of making effective decisions and demonstrate a high degree of personal credibility.
Varaktighet, arbetstid
100 %. Tillträde: Omgående Visstidsanställning
ErsättningMånadslön
Så ansöker duSista dag att ansöka är 2016-03-06
Ange följande referens när du ansöker: 661177
Klicka på denna länk för att göra din ansökanFöretagAstraZeneca / Proffice Link AB
AdressAstraZeneca / Proffice Link AB
Kungsgatan 57 A, Box 207
10124 Stockholm
KontorsadressKungsgatan 57 A, Box 207
Jobbnummer 2684773
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