Quality Control Manager

The Quality Control Manager applies extensive knowledge of clinical radiopharmaceuticals to ensure the quality of investigational radiopharmaceuticals specified by the standards stated in the USP Chapter <823> and the laboratory requirements of 21 CFR 212. This position will report to the Director of the Radiopharmaceutical Facility in the development of quality control standard operating procedures for the investigational PET drugs such that the facilities, equipment, and inventory control meet the associated regulatory requirements.

This position will also assist in creating new approaches in the quality control of novel radiopharmaceuticals for clinical use, and in working with the director in writing investigational drug applications (IND) and Abbreviated New Drug Applications (ANDA). The background for this position requires a minimum of a BS in chemistry or related subject with at least 5 years experience in a GMP radiopharmaceutical facility.

Required Qualifications Bachelor’s degree in Chemistry, Pharmacy, or a related field Minimum of 5+ years of related experience 3 years of experience in quality control of cGMP PET radiopharmaceuticals Advanced ability to effectively lead one or more projects with competing priorities to meet the demands of a fast-paced and dynamic work environment; adaptable to quickly changing priorities In-depth critical thinking skills to evaluate issues and identify potential solutions; creatively addresses complex or new problems Advanced interpersonal skills, including but not limited to problem-solving, teamwork development, and leadership with other team members; works well with others to achieve common goals

Master’s degree in Chemistry, Pharmacy, or a related field Knowledge of 21 CFR 212 and USP <823> regulatory requirements

Day shift