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 21CFR parts 210 and 211, knowledge of the FDA Guidance for Sterile Drug Products Produced by Aseptic Processing – cGMP, and EU GMP Annex 1: Manufacture of Sterile Medicinal Products. Candidate will be responsible for managing the quality team, establishing the quality policy for media fills, parenteral manufacturing, and quality procedures that support parenteral manufacturing. Duties to include review of qualification and validation documents for all processes and equipment including protocols and summary reports, risk assessments, investigations, SOPs to support the quality program, and establishment of the sterility assurance plan and contamination control strategy. QCL offers competitive salaries commensurate with experience and an excellent benefits package, as well as great potential for career advancement and leadership in a rapidly growing company. We now also offer subsidized childcare at our 5-Star childcare facility. Qualified candidates may apply via our website by clicking APPLY NOW below, or email resumes to [email protected].