Quality Assurance Advisor to AstraZeneca in Mölndal!
Adecco Sweden AB / Biologjobb / Mölndal
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hela Sverige Addecco life Science is now able to offer the possibility to work as a Quality Assurance Advisor at AstraZeneca in Mölndal! The assignment is a consultant assignment which is planned to start preferably 2017-06-01 and proceed for one year.
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 Quality Assurance, for one of the world 's leading pharmaceutical companies?
Pharmaceutical Development is the function within AstraZeneca that designs and delivers the active drug product required to support new medicines. The Quality Assurance group within Pharmaceutical development now wants to take in Quality Assurance contractors 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 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
In your work as a 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.
• Provide QA advise into Pharmaceutical Development internal/external manufacturing activities for Drug Product
• 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 and other quality and compliance decisions having a major impact on AstraZeneca development projects
• Provide Pharmaceutical Development projects with QA support, such as GMP risk assessment and interpretation of GMP regulations
• Provide appropriate QA input to business improvement projects
• Close collaboration with AstraZeneca QA colleagues globally
The role may also include
• Responsible for QA 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 Pharmaceutical Development.
• Developing 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
Vad erbjuder vi?
Adecco Life Scienceär ett specialiserat affärsområde inom Adecco som enbart arbetar med uthyrning och rekrytering av personal inom Life Science. Vår expertis finns inom alla områden av Life Science som t.ex. FoU, Produktion, Kvalité, Kliniska prövningar, och Marknad & Försäljning för att nämna några. Våra kunder finns inom hela Läkemedels-, MedTech-, och BioTech- industrin runt om i Sverige. Vi förmedlar bl.a. forskare, laboratorieingenjörer, kvalitetsingenjörer, kliniska prövningsledare och läkemedelskonsulenter. Som världens största rekryterings- och bemanningsföretag är vår viktigaste tillgång våra kvalificerade medarbetare. Hos oss kommer du som konsult att uppskattas för din specifika kompetens inom Life Science.
Adecco Life Science kan erbjuda dig möjligheten till intressanta uppdrag på attraktiva företag och till tjänster som kanske aldrig kommer ut på den öppna marknaden! För din trygghet omfattas du självklart av kollektivavtal och även av försäkringar och företagshälsovård. Vi vill också att du ska må bra och ger dig bl.a. friskvårdsbidrag och rabatter på träningskort.
Är du intresserad?
Tveka inte med din ansökan! Då uppdraget ska tillsättas så snart som möjligt sker rekrytering löpande under ansökningstiden.
Vid frågor angående registrering på hemsidan kontakta kandidatsupport tel: 08- 598 980 10.
Tyvärr kan vi inte ta emot ansökningar via mail men om du har frågor rörande tjänsten kontakta Nalin Yilmaz,
nalin.yilmaz@adecco.seVarmt välkommen med din ansökan!
Varaktighet, arbetstid
Heltid Tillsvidare
Publiceringsdatum2017-05-19ErsättningFast lön
Så ansöker duSista dag att ansöka är 2017-05-24
Klicka på denna länk för att göra din ansökanKontaktNalin Yilmaz
nalin.yilmaz@adecco.seFöretagAdecco Sweden AB
AdressAdecco Sweden AB
Kungsgatan 60
10224 STOCKHOLM
KontorsadressKungsgatan 60
Jobbnummer 3511556
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