Quality Manager

Quality ManagerNew Castle, DE$130,000–$150,000 annuallyMonday–Friday | 8:00 AM – 5:00 PMDirect HirePosition Overview:Do you have experience leading quality systems and ensuring compliance in a cGMP manufacturing environment? In this role, you will oversee quality assurance and quality control programs, manage audits and documentation, and support continuous improvement initiatives.Responsibilities:Oversee Quality Assurance programs and regulatory complianceManage CAPA, HARPC, OOS, change control, and nonconformancesWrite, review, and approve SOPs and GMP documentationConduct audits and product inspectionsReview and maintain quality records and documentationServe as point of contact for FDA and third-party auditsMonitor quality metrics and report findings to senior managementRequirements:Bachelor’s degree in Chemistry, Biochemistry, or related field required10+ years of experience in a cGMP manufacturing environment5+ years of supervisory and project management experienceStrong knowledge of cGMP regulations and FDA complianceExperience managing audits and regulatory inspectionsStrong documentation, auditing, and process improvement skillsApply Today!