Great contract- opportunity for Quality Professionals who are committed to working under the highest standards of integrity and ethics! Qualified candidates will have the opportunity to produce products of excellent quality and reliability within a company looking to expand their Quality Department. Our client is a leader in the development and manufacturing of specialty injectable pharmaceuticals and they have several opportunities available for Quality Professionals looking to work in Rocky Mount North Carolina who meet the following qualifications:

Requirements:

• Bachelor's Degree or Master's degree in a life science
• At least 3 years of investigations, technical writing, CAPA, root cause analysis, auditing experience in a cGMP environment
• Knowledge of at least one of the following: Pharmaceutical Manufacturing, Analytical Chemistry (HPLC, GC, Karl Fischer), Validation (IQ/OQ/PQ), QA Auditing

Responsibilities:

• Investigate deviations, OOS, OOT, non-conformances
  Initiate CAPA methods in compliance with GMP standards
• Work with Laboratory, Manufacturing and Senior Management to develop strategic investigation plans
  Perform Root Cause Analysis from deviations
• Technical Writing (Deviation reports, LIRs, MIRs, IQ/OQ/PQ, SOPs, etc.)
• Perform QA Audits of Manufacturing & Laboratory areas

For immediate consideration, please click Apply Now

Kelly Scientific Resources (KSR) is the leading scientific and clinical research staffing company in the world. We employ more than 700 clinical research professionals and 4,500 scientists on an average workday on a temporary, project and full-time basis in a broad spectrum of industries and disciplines. KSR has more than 100 locations in North America, Europe and the Pacific Rim. Please visit us at www.kellyscientific.com to learn more. Kelly Services is an Equal Opportunity Employer.