Quality Assurance Advisor at AstraZeneca - Proffice Life Science AB - Apotekarjobb i Göteborg
Quality Assurance Advisor at AstraZeneca
Proffice Life Science AB / Apotekarjobb / Göteborg
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Quality Assurance Advisor at AstraZeneca
Do you have experience from working within the supply chain and release of new substances? This is an exciting opportunity for you to work with Quality Assurance at AstraZeneca, Mölndal in Sweden.

Don't hesitate to send your application for this position, both English and Swedish applications will be accepted. You don't need to be certified or worked as a QP but will gain from having experience from working in the supply chain.

Pharmaceutical Development's Quality Assurance (QA) function is recruiting a QA Advisor with a Good Manufacturing Practice (GMP) focus for one-year temporary contract. The QA Advisor role has a broad range of responsibilities to ensure that activities and processes in Pharmaceutical Development functions and the R&D supply chain comply with Regulatory requirements, Good Manufacturing Practices and AZ internal quality system requirements.

Interactions occur among various internal functions and sites, but also with vendors and suppliers. The role is based at Mölndal in Sweden.

Business: Dfind Science & Engineering

City: Göteborg

The role

* Provide QA input into Pharmaceutical Development internal/external manufacturing activities for Drug Substance and Drug Product, the approval of manufacturing documentation
* QA release of internally/externally manufactured and packed Drug Substance and 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.

Minimum requirements

* Scientific degree 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 experience/requirements

* Experience preferably within a pharmaceutical development organization
* Good team working and networking skills
* Capable of making effective decisions
* Demonstrate a high degree of personal credibility

Deadline for applications: 2014-09-23

More information: Per Hillertz, 0733-434018 or Eleonor Ehrman 0733-434109

Organization/Business description:
Dfind Science & Engineering är ett konsult- och rekryteringsföretag specialiserade på kompetenser inom naturvetenskap och teknik. Med engagemang och lyhördhet hjälper vi människor och företag att hitta lösningar för att utvecklas. Hos oss har du möjlighet att utveckla dina kunskaper och färdigheter genom uppdrag hos våra utvecklings- forsknings- och produktionsintensiva kunder i Norden.

Vi tycker att det är viktigt att all kompetens på arbetsmarknaden tillvaratas. Vi välkomnar alla sökande och eftersträvar mångfald. Dfind Science & Engineering ett auktoriserat bemanningsföretag via Almega och följer deras kollektivavtal.

Publiceringsdatum
2014-09-17

Arbetstider och omfattning
Heltid Visstid

Ersättning
Fast lön

Så ansöker du
Sista dag att ansöka är 2014-09-23
Ange följande referens när du ansöker: 200639880
Klicka på denna länk för att göra din ansökan

Kontakt
Per Hillertz per.hillertz@dfind.se

Företag
Proffice Life Science AB

Adress
Proffice Life Science AB
Östra Hamngatan 23
41110 GÖTEBORG

Kontorsadress
Östra Hamngatan 23, 41110 GÖTEBORG

Jobbnummer
1999854

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