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QA Specialist II (Dublin or Limerick based, perm)

015856_2

About the role

This vacancy has now expired. Please click here to view live vacancies.

Are you interested in joining ICON in leading regulatory compliance audits, driving CAPA's, developing SOP's and integrating corporate quality management systems?
Auditor role within ICON:
ICON Clinical Research has a strong reputation in our approaches to clinical development and provides innovative strategies to the drug development process. Quality Assurance Specialist work closely with management teams, internal/external clients and vendors or suppliers of ICON. You will develop and manage SOP's while also reviewing and approving Systems Development Life Cycle Role (SDLC) documentation to assure regulatory compliance.
To succeed you will need:
We are seeking a bachelor's degree and quality assurance experience with a strong working knowledge of GCP, ICH and QA Principles. Successful candidate will have experience within a Pharmaceutical, Biotech company or CRO. One will need to have a working knowledge of SDLC methodology, computer system validation and 21 CFR Part 11 including auditing against these regulations. In order to travel we may require a valid driver's license and the willingness to travel up to 10% when needed.
We invite you to review our opportunities at www.iconplc.com/careers.

What's Next?
Following your application you will be contacted by one of our dedicated recruiters and if successful we will be able to provide you with more details about this opportunity.
ICON is an equal opportunity employer - M/F/D/V and committed to providing a workplace free of any discrimination or harassment. Applications will close July 27, 2015.
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