Company: Barrington James Scientific
Reference: CCT GLP
Closing Date: 08 Jan 17
Salary (£): Competitive
A new Quality Assurance Auditor contract opportunity for a reputable early drug development CRO!
A new client of mine who are well on their way to becoming the most trusted and preferred early drug development CRO on the East Coast are looking for a team of GLP QA Auditor for a contract opportunity!
...have to have a working experience within the pre clinical realm with a minimum of 6 years working within GLP quality.
...have to have a bachelor's/ master's degree in a life science related discipline.
...ideally be RQAP - GLP certified.
What you will be doing
You will be working as part of a team to achieve time specific deadlines to meet clients expectations. So having the ability to work under pressure is key! You should have working experience in performance of data and report audits according to protocols (GLP's, SOP's), and having an extensive knowledge of pharma research and development processes - as this is a major part of the requirements needed.
You will ideally be located in Michigan, however out of state candidates may be considered at no extra cost to the client. This is a position for an independent consultant who is looking to carry on their professional experience working with a reputable CRO.
Submit your application/ resume to me at email@example.com - and call me on 646 415 8221 to discuss this position on more of a personal level!
*Referral scheme* - if you refer a friend or colleague to me that would benefit about hearing from this role, and they get placed - you will receive $500!
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