Quality Assurance Advisor
AstraZeneca / Kemiingenjörsjobb / Göteborg
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hela Sverige Visa alla jobb hos AstraZeneca i Göteborg,
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hela Sverige Are you interested in a challenging opportunity within the Development Quality function in one of the world's leading pharmaceutical companies?
As a Quality Advisor, you will have a broad range of responsibilities to ensure all internal and external requirements are fulfilled for the AstraZeneca projects in the development phase. You will also have the possibility to contribute with expert advice to the pharmaceutical development functions and to the delivery of our pipeline of exciting new medicines.
You will be part of the Development Quality function is responsible for quality oversight of the pharmaceutical development activities in AstraZeneca. We at AstraZeneca's pharmaceutical development organizations deal with all facets of the process of turning a molecule into a medicine which can be safely and effectively used by patients.
The role
In your role you will have a lot of interactions with internal and external stakeholders as well as with vendors and suppliers.
* Provide QA advice into internal/external manufacturing activities of Drug Product and patient medication
* Perform QA release of internally/externally manufactured and packed Drug Product as part of the Supply Chain to clinical trials
* Support the pharmaceutical development functions with investigations of deviations, complaints, changes and other quality and compliance decisions in the development projects
* Provide QA support to pharmaceutical development project with interpretation of GMP regulations
* Provide appropriate QA input to business improvement projects
* Collaboration with AstraZeneca QA colleagues globally
The role may also include
* Responsible for QA advice and approval of documentation related to manufacturing equipment and facilities to ensure compliance, including maintenance, calibration, validation and change control
* Interpret, trend and report compliance data, to measure and improve quality standards within the pharmaceutical development functions.
* Develop QA Agreements with suppliers or contractors delivering services or products to the pharmaceutical development Supply Chain.
Minimum requirements - Education and Experience
* MSc in pharmacy or engineering (specializing in Pharmaceuticals) with at least 3 years' experience of working within a pharmaceutical GMP environment
* Broad understanding of Quality Systems and GMP
* Comprehensive understanding of the pharmaceutical/drug development process
* Good communicator with experience of interacting effectively across interfaces
* Fluent in written and spoken English
Preferred requirements
* Experience preferably within a pharmaceutical manufacturing organization
* Good team working and networking skills
* Capable of making effective decisions
* Demonstrate a high degree of personal credibility
If you are interested, apply now!
If you want more information, please contact hiring manager Bodil Egeland at +46(0)31 706 47 01.
We encourage you to send your application as soon as possible, since interviews will be held continuously, but no later than Thursday the 22th of Feb, 2018.
AstraZeneca is an equal opportunity employer. AstraZeneca will consider all qualified applicants for employment without discrimination on grounds of disability, sex or sexual orientation, pregnancy or maternity leave status, race or national or ethnic origin, age, religion or belief, gender identity or re-assignment, marital or civil partnership status, protected veteran status (if applicable) or any other characteristic protected by law.
Varaktighet, arbetstid
Heltid Permanent
Publiceringsdatum2018-02-01ErsättningNot Specified
Så ansöker duSista dag att ansöka är 2018-02-20
Ange följande referens när du ansöker: R-021803
Klicka på denna länk för att göra din ansökanKontaktAstraZeneca
daniela.borquez@astrazeneca.comFöretagAstraZeneca
AdressAstraZeneca
43183
43183 1480
KontorsadressPepparedsleden 1
Jobbnummer 3938164
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