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An established industry player in pharmaceutical testing is on the lookout for a meticulous QA Associate focused on report generation. This role is crucial in ensuring the accuracy and completeness of laboratory reports, including certificates of analysis and stability study tables. The ideal candidate will possess exceptional attention to detail and strong documentation skills, along with proficiency in Microsoft Word. This position not only offers competitive salaries but also presents excellent opportunities for career growth and leadership within a rapidly expanding company. If you thrive in a detail-oriented environment and are eager to contribute to quality assurance, this is the perfect opportunity for you.
Quality Chemical Laboratories (QCL), a leading Pharmaceutical testing and manufacturing laboratory in Wilmington, is seeking a qualified candidate for the position of QA Associate – Report Generation. 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 offers competitive salaries commensurate with experience and an excellent benefits package as well as great potential for career advancement and leadership in a rapidly growing company.