Poolia Life Science · Publicerad 8 okt 2019

Are you a highly motivated and skilled Combination Product Quality Engineer within medical device? Then this 12-months consultant position at AstraZeneca, starting as soon as possible, can be right for you! To be considered for this exciting opportunity, please complete the application at your earliest convenience. If you know someone who would be a great fit, please share this posting with them.

Om tjänsten

As Quality Engineer you will be a key of a cross functional development for the development of an inhaler. You will ensure that the projects are delivered with the highest quality and compliant to requirements from Health Authorities, Regulations and Standards. You will be responsible to ensure that the right processes, procedures and best practices are executed and implemented in the projects.

Dina arbetsuppgifter i huvudsak

Activities typically includes, but limited to:
  • Work proactively with development team to plan, develop, and deliver medical devices and combination products that are of the highest quality and also satisfies user needs.
  • Ensure project team follow processes, procedures, ways of working and templates
  • Ensure the project is compliant to applicable regulations, laws and standards
  • Facilitate risk assessment events and ensure that risks process is executed
  • Provide expert knowledge to the project team when it comes to GXP ways of working
  • Ensure documentation are written a quality and regulatory way
  • Be a link between the QA, Medical Device Regulatory Affairs and the project team
  • Work with other Quality Engineer to drive harmonization across project and execute quality engineering initiatives
  • Author DHF index and Essential Requirements List
  • Ensure high quality and compliant DHF by review project team documentation
Vem är du?

Minimum requirements:
  • 5+ years' experience working in development of medical devices or other relevant regulated industry
  • 3+ years´ experience working in a Medical Device Quality or Regulatory department
  • Extensive understanding of process for development of Medical Devices and Combination Products; MDD, ISO 13485, FDA 21 CFR 820 and FDA 21 CFR 4
  • Experience in establishing DHFs, Technical Files and Dossiers
  • Good understanding for medical device technical standards; ISO, IEC FDA guidelines
  • Excellent organizational and communication (oral and written) skills.
  • Ability to work on teams as well as individually
  • Ability to be pragmatic but still be compliant to solve problems
  • Good leadership and interpersonal skills
  • Good technical and regulatory writing skills
  • Fluent in English
Om verksamheten

AstraZeneca is a major international healthcare business engaged in the research, development, manufacture and marketing of prescription pharmaceuticals and the supply of healthcare services. AstraZeneca is proud to offer a unique workplace culture that inspires innovation and collaboration. Co-workers are empowered to express diverse perspectives - and are made to feel valued, energized and rewarded for their ideas and creativity.
+ Läs mer om jobbet
Sista ansökningsdag
18 okt 2019
Anställning
Tillsvidareanställd
Omfattning
Heltid
Antal Tjänster
1
Yrkesområde
Data & IT

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