Quality Assurance Specialist

Limerick  ‐ Vor Ort
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Beschreibung

Are you interested in joining our client in integrating new products into a regulated SDLC, driving process improvement, and developing quality management systems?

As a Quality Assurance Specialist role:
Our client has a strong reputation in our approaches to clinical development and provides innovative strategies to the drug development process. The Senior Quality Assurance Specialist works closely with management teams, internal/external clients and vendors or suppliers. You will develop and manage SOP’s while also reviewing and approving Systems Development Life Cycle Role (SDLC) documentation to assure regulatory compliance.

Our client is presently in over 40 countries with over 80 offices worldwide and over 11,000 employees globally. In this role you will be working closely with Clinical Development and Software Development Teams in bringing new technology to the fore via their SDLC process.

To succeed you will need:
They are seeking a Bachelor’s degree and at least 3 years of Quality Assurance experience with a strong working knowledge of GCP, GxP and QA Principles. Successful candidate will have experience within a Pharmaceutical, Medical Device 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.

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.
Our client is an equal opportunity employer - M/F/D/V and committed to providing a workplace free of any discrimination or harassment.
Start
03.2016
Dauer
6 Monate
(Verlängerung möglich)
Von
Antal International
Eingestellt
16.02.2016
Ansprechpartner:
Alessandro Moretta
Projekt-ID:
1070468
Vertragsart
Freiberuflich
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