A biotechnology company in Alabama is seeking a detail-oriented Site Quality Lead. This role involves ensuring compliance with FDA and cGMP standards in radiopharmaceutical manufacturing. The ideal candidate should have a Bachelor's degree in a scientific field and 3+ years of experience in pharmaceutical quality assurance. Responsibilities include maintaining quality systems, supporting audits, and delivering compliance training. Competitive compensation and benefits are offered, including an annual performance bonus and generous vacation. #J-18808-Ljbffr