PAREXEL has supported the Bio-Tech and Pharmaceutical industries in helping the development of new drugs and treatments on a global basis. As a leading global biopharmaceutical service provider, they supply knowledge-based contract research, medical communications and consulting services across a broad range of therapeutic areas to the worldwide pharmaceutical, biotechnology and medical device industries. They have helped over 800 clients to develop and launch some of the most important drugs and devices of our time-helping people live better and healthier lives everywhere in the world. Headquartered near Boston, Massachusetts, PAREXEL operates in more than 50 countries around the world.
Post: Senior Quality Specialist, RRC
Job Description
Quality Specialist must be detail oriented, able to support the processing of Sponsor Audits & Regulatory Inspections (SA & RI) in QuIPS, including classification, QC and metrics; assist in the development and update of SA & RI SOPs and training packages; exhibit a high degree of flexibility and initiative, demonstrate the ability to follow up on multiple tasks, and possess the ability to handle confidential information diplomatically.
Candidate Profile
Experience in quality assurance, regulatory affairs, auditing, clinical research, monitoring, data management, pharmacy, laboratory, or other relevant area, including applicable GxP auditing
Additional Information:
Location: Andhra Pradesh - Hyderabad
Functional Area: Other
Requisition: pare-10038104
Industry Type: Pharma/ Biotech/Clinical Research
Employment Type: Full Time
Job Type: Regular
End Date: 15th November, 2014
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