AstraZeneca: Quality Assurance Advisor
Experis Engineering / Kemiingenjörsjobb / Göteborg
Observera att sista ansökningsdag har passerat.
Visa alla kemiingenjörsjobb i Göteborg,
Mölndal,
Partille,
Kungälv,
Lerum eller i
hela Sverige Visa alla jobb hos Experis Engineering i Göteborg,
Mölndal,
Kungsbacka,
Stenungsund,
Ale eller i
hela Sverige AstraZeneca is a global, innovation-driven biopharmaceutical business that focuses on the discovery, development and commercialization of prescription medicines for some of the world's most serious diseases. But we're more than one of the world's leading pharmaceutical companies. At AstraZeneca, we're proud to have a unique workplace culture that inspires innovation and collaboration. Here, employees are empowered to express diverse perspectives - and are made to feel valued, energized and rewarded for their ideas and creativity.
For a consultant assignment during 3 months at AstraZeneca in Mölndal we are now looking for a Quality Assurance Advisor with experience from pharmaceutical development.
The arena
Pharmaceutical Development's Quality Assurance (QA) function at the R&D site in Mölndal is recruiting a QA Advisor with a Good Manufacturing Practice (GMP) focus for a permanent position. AstraZeneca's Pharmaceutical Development organization deals with all facets of the process of turning a new chemical entity (NCE) into a medication which can be safely and effectively used by patients in the community. The QA Advisor role has a broad range of responsibilities to ensure internal and external requirements are fulfilled for AstraZeneca projects in the development phase. Interactions occur among various internal functions and sites, but also with vendors and suppliers.
The role
• Writing Quality Assurance Agreements, Site Management Plan and Validation Plan.
• Close collaboration with AstraZeneca QA colleagues in Sweden, as well as in the UK and US.
Minimum experience
• GMP experience and experience as Qualified Person
• Scientific degree with experience of working within a pharmaceutical GMP environment
• Broad understanding of Quality Systems and GMP
• Comprehensive understanding of the pharmaceutical/drug development process
• Fluent in written and spoken English
Preferred experience/requirements
• Good team working and networking skills
• Capable of making effective decisions
• Demonstrate a high degree of personal credibility
Contact/Application
If you are the person we are looking for you are welcome to apply for this job through the link on this site. The selection process will be short so please send in your application as soon as possible with CV and personal letter written in English. Do not hesitate to contact Cunsultant Manager Tomas Niregård, at Experis Engineering, for further questions:
tomas.niregard@se.experis.com , 031-61 72 59.
Publiceringsdatum2014-04-11Arbetstider och omfattningEnligt överenskommelse
ErsättningEnligt överenskommelse
Så ansöker duSista dag att ansöka är 2014-04-17
Klicka på denna länk för att göra din ansökanKontaktTomas Niregård
FöretagExperis Engineering
AdressExperis Engineering
BOX 1125
11181 Stockholm
Jobbnummer 1839690
Observera att sista ansökningsdag har passerat.