Quality Assurance Advisor - Secondment 12 months
AstraZeneca / Elektronikjobb / Göteborg
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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.
The arena
Are you interested in a challenging opportunity within the Development Quality function in one of the world's leading pharmaceutical companies?
The Development Quality function is responsible for quality oversight of the pharmaceutical development activities in AstraZeneca. We are now looking for a Quality Advisor with GMP focus to our Gothenburg team. 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 Quality Advisor role has 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.
Main Duties and Responsibilities
As a Quality Advisor, you will be responsible for review and approval of information provided by internal and external providers, including labelling information, batch and disposition documentation. You will assist client groups in ensuring any deviations and investigations are appropriately investigated and documented and act as Subject Matter Expert supporting internal and external audits and visits to contractor facilities as required.
You will support QA management in ensuring the systems and procedures used by AstraZeneca are fit for purpose and appropriately maintained and identify and implement improvements to AstraZeneca's systems and procedures. You will ensure practices are conducted in compliance with company policies and site procedures.
Additionally, you will assist in investigations related to non-conformances, vendor reported deviations, trend analyses, and product complaints using Quality Systems tools such as FMEA and Root Cause Analysis. Upon gaining the relevant experience and knowledge of AstraZeneca systems, you will provide Quality and GMP support to CMC project team(s) and assigned projects.
Minimum requirements - Education and Experience
* BSc in a relevant scientific discipline with at least 3 years' experience of working within a pharmaceutical GMP environment
* Broad understanding of Quality Systems and GMP
* 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
* Comprehensive understanding of the pharmaceutical/drug development process
* Capable of making effective decisions
* Experience of GMP auditing
Demonstrate a high degree of personal credibility.
If you are interested, please apply now!
For more information about the position please contact Richard Brown, Richard.
Welcome with your application no later than January 21st, 2019.
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. AstraZeneca only employs individuals with the right to work in the country/ies where the role is advertised.
Varaktighet, arbetstid
Heltid Temporary
Publiceringsdatum2018-12-18ErsättningNot Specified
Så ansöker duSista dag att ansöka är 2019-01-06
Ange följande referens när du ansöker: R-041187
Klicka på denna länk för att göra din ansökanKontaktAstraZeneca
sara.jagevall@astrazeneca.comFöretagAstraZeneca
AdressAstraZeneca
43183
43183 1480
KontorsadressPepparedsleden 1
Jobbnummer 4515789
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