Experience with working in an R&D environment for clinical trials is preferred. 3-5 years experience with quality assurance reviewing documentation for errors. Attention to detail is required for this role, this will be assessed on the resumes submitted. Minimum education requirement is a Bachelor’s degree in the scientific fields.
In the R&D Clinical Trial space:
• Review and recommend release for a range of R&D dosage forms and finished clinical trial packs of Investigational Medicinal Products in accordance with GMP/GSK requirements.
• Assessment of Quality Deviations, Customer Complaints, Change Controls and Vendor Complaints and make recommendations for corrective and preventative actions, and to follow up on the implementation of those recommendations
• Provide advice and support to R&D business partner areas relating to quality matters and process improvement.
SRG is an Equal Opportunity Employer - All qualified applicants will receive consideration without regard to race, color, religion, gender, national origin, age, disability, veteran status, or any other factor determined to be unlawful under applicable law.
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