Director of Quality Control

Qualification

Education/Experience: Master’s or PhD in Chemistry, Biochemistry, Microbiology, Pharmaceutical Sciences, or related discipline preferred. A bachelor’s degree with extensive experience may be considered. 10+ years of experience in QC within pharmaceutical or biopharmaceutical manufacturing. 5+ years of leadership/management experience in a GMP laboratory setting. Experience preparing for and hosting inspections by FDA, EMA, or other health authorities. Strong background in analytical chemistry and/or microbiology. Experience with method validation, QC automation, LIMS/ELN, and electronic data management systems. Knowledge, Skills, and Abilities: Deep knowledge of cGMP, ICH guidelines, USP/EP, and regulatory expectations. Strong scientific judgment and technical problem-solving skills. Excellent leadership, communication, and interpersonal skills. Ability to manage multiple priorities and drive timely execution. Demonstrated ability to develop high-performing teams and a culture of quality and compliance. Requirements: Must live or be willing to move to the Sacramento Metropolitan Region (Approx 40 miles’ radius) Benefits: Pay range: Competitive Salary Range $200-245K Annually; Based