Nexhireplus
AQA QA Associate II - Central Islip, NY
Nexhireplus, Central Islip, New York, United States, 11722
Job Title:
AQA QA Associate II
Remember to check your CV before applying Also, ensure you read through all the requirements related to this role. Location:
Central Islip, NY Employment Type:
Full-time Overview: A leading pharmaceutical company is seeking an experienced AQA QA Associate II to join its quality assurance team in Central Islip, NY. The ideal candidate will have significant analytical laboratory experience and a strong understanding of cGMP, GLP, and documentation practices. Key Responsibilities: Perform analytical quality assurance activities in pharmaceutical laboratory environments. Operate, qualify, and calibrate key laboratory equipment (e.g., HPLC, UV-Vis spectrophotometer, GC, pH meter, stability chambers). Conduct and review analytical testing and data following cGMP/GLP/GDP guidelines. Ensure compliance with USP monograph requirements, FDA and ICH guidance, and internal SOPs. Review laboratory records, audit trails, calibration logs, and analytical data. Maintain thorough documentation and support internal and external audits and inspections. Collaborate cross-functionally with Quality, Production, and R&D teams. Support ongoing improvement of analytical procedures and compliance processes. Follow all personal protective equipment and safety requirements in laboratory and production settings.
AQA QA Associate II
Remember to check your CV before applying Also, ensure you read through all the requirements related to this role. Location:
Central Islip, NY Employment Type:
Full-time Overview: A leading pharmaceutical company is seeking an experienced AQA QA Associate II to join its quality assurance team in Central Islip, NY. The ideal candidate will have significant analytical laboratory experience and a strong understanding of cGMP, GLP, and documentation practices. Key Responsibilities: Perform analytical quality assurance activities in pharmaceutical laboratory environments. Operate, qualify, and calibrate key laboratory equipment (e.g., HPLC, UV-Vis spectrophotometer, GC, pH meter, stability chambers). Conduct and review analytical testing and data following cGMP/GLP/GDP guidelines. Ensure compliance with USP monograph requirements, FDA and ICH guidance, and internal SOPs. Review laboratory records, audit trails, calibration logs, and analytical data. Maintain thorough documentation and support internal and external audits and inspections. Collaborate cross-functionally with Quality, Production, and R&D teams. Support ongoing improvement of analytical procedures and compliance processes. Follow all personal protective equipment and safety requirements in laboratory and production settings.