2 21 CFR Part 11 Jobs in the South East

Knowledge of global regulatory requirements for pharmaceutical, medical devices and combination products. • Knowledge of FDA Quality Systems, pharmaceutical products, and Medical Device Reporting regulations (21 CFR 803, 820 and 211) is preferred. • Ability to prioritize multiple projects to ensure compliance with regulations and standard operating procedures is preferred. more »

using industry-standard software lifecycle management tools such as Jira, Confluence, and AHA! Previous exposure to applying industry compliance and quality standards (GLP, GMP, 21CFRPart11) in software products. Effective communication and stakeholder management skills to facilitate seamless collaboration and alignment across diverse stakeholders. If you possess a passion for driving … innovation in the biopharma sector and are equipped with the requisite skills and experience, we encourage you to apply and be a part of our transformative journey. more »