Lead Quality Assurance Advisor, R&D GMP setting
AstraZeneca Mölndal / Smedsjobb / Mölndal
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Are you interested in a challenging opportunity within Quality Assurance, for one of the world's leading pharmaceutical companies?
In your work as a Lead Quality Advisor at AstraZeneca you will have a broad range of responsibilities, the possibility to influence and to contribute to the pharmaceutical development function, and the delivery of our pipeline of exciting new medicines.
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
Pharmaceutical Development?s Quality Assurance group is recruiting a Lead Quality Advisor with a Good Manufacturing Practice (GMP) focus. AstraZeneca's Pharmaceutical Development organization deals with all facets of the process of turning a new chemical entity (NCE) into a medicine which can be safely and effectively used by patients. The Lead Quality 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
Provide expert support and guidance to Pharmaceutical Development Functions to satisfy external Regulatory Authority GMP inspections and support implementation of agreed global standards.
Develop and contribute to the internal and external audit plan and carry-out QA/GMP internal and external audits.
Owner of a number of Quality Management systems/processes and lead continual improvement of these systems in line with new GMP regulations.
Responsible for Quality Management of suppliers or contractors delivering services or products to the Pharmaceutical Development Supply Chain.
Minimum requirements - Education and Experience
Appropriate scientific degree with extensive experience (5-10 years) of working within a pharmaceutical GMP environment
Extensive experience from working in a Quality Assurance function is essential
A broad and comprehensive understanding of Quality Systems and GMP
A comprehensive understanding of the pharmaceutical/drug development process
Fluent in written and spoken English
Preferred requirements
Excellent team working and networking skills and encourages team effectiveness
Demonstrates independent judgement and uses risk management in complex situations
Capable of making decisions, acting courageously and communicating with conviction and inspiration
A good communicator with experience of interacting effectively across interfaces
Builds excellent relationships both internally and with external suppliers or service providers
Demonstrate a high degree of personal credibility
This role may be based at the R&D sites in Gothenburg, Sweden or Macclesfield, the UK..............FOR FULL JOB DESCRIPTION AND TO APPLY, please visit
www.astrazeneca.se/karriarVaraktighet, arbetstid
Tillsvidare
Heltid
Publiceringsdatum2015-10-23ErsättningFast månads- vecko- eller timlön
Så ansöker duSista dag att ansöka är 2015-11-15
Ange följande referens när du ansöker: GOT00000001
FöretagAstraZeneca Mölndal
AdressAstraZeneca Mölndal
43183 MÖLNDAL
KontorsadressPEPPAREDSLEDEN 1
MÖLNDAL
Övriga kontaktuppgifterTelefonnummer: 031-7761000
Jobbnummer 2495437
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