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Quality Chemical Laboratories (QCL) in Wilmington, NC, is seeking a QA Associate – Report Generation to join our quality team. The role focuses on reviewing and approving reports generated from laboratory data, including certificates of analysis and stability tables, ensuring accuracy and GMP/SOP compliance.
The successful candidate will demonstrate meticulous documentation, strong communication, and problem-solving skills.
The candidate will be responsible for review and approval of reports generated from laboratory data, such as certificate of analysis and stability study tables and will be expected to review reports for completeness and accuracy to ensure compliance with GMPs and SOPs.
This position requires outstanding attention to detail, documentation, communication, problem-solving and organization skills. With experience, the candidate may be required to review technical reports such as method verifications, validations, transfer activities and other protocol driven work. Candidate must be proficient in Word and formatting documents. Additional quality assurance responsibilities may be required.
QCL is an equal opportunity employer.