Quality Chemical Laboratories (QCL), a pharmaceutical testing, manufacturing, and development lab in Wilmington, is seeking a highly motivated candidate for Quality Manager for our sterile fill-finish parenteral manufacturing facility. Requires high-level quality experience in sterile manufacturing, knowledge of 21 CFR parts 210 and 211, FDA Guidance for Sterile Drug Products Produced by Aseptic Processing – cGMP, and EU GMP Annex 1: Manufacture of Sterile Medicinal Products. Responsibilities include managing the quality team, establishing quality policy for media fills and parenteral manufacturing, quality procedures, review of qualification and validation documents, risk assessments, investigations, SOPs to support the quality program, and establishment of the sterility assurance plan and contamination control strategy.