Description
A well established biopharmaceutical company is looking for a GCP Quality Specialist to join their team. The qualifications they are looking for are listed below,Responsibilities:
-Plan and conduct audits independently
-Draft and finalize audit reports
-Work closely with Project Management, Clinical (Study) Operations, Quality Management and Quality Assurance (Research Regulatory compliance) groups
-Travel to perform audits (e.g Investigator Site audits)
Experience:
-Bachelor's degree in life science or related field
-Substantial experience in GCP audits
-Excellent interpersonal, verbal and written communication skills
-Ability to develop relationships with culturally diverse groups, stakeholders within PXL and clients
-Excellent analytical skills
-Excellent organization skills, ability to manage multiple tasks or projects and prioritize a workload
-Solid knowledge of GCP, ICH and FDA regulations and guidelines
-Ability to travel frequently
-Minimum 5 years experience in the pharmaceutical industry
If you meet the qualifications listed above please submit your resume ASAP for consideration.
To find out more about Real please visit www.realstaffing.com