Quality Manager (Pharma Packaging)

Why Join Liveo Research?Career stability with opportunities for advancementComprehensive benefits package: medical, dental, vision401(k) with generous company matchShort-term and long-term disability, company-paid life insuranceAbout Liveo ResearchLiveo Research is a leading global manufacturer of rigid packaging solutions, with five strategically located facilities worldwide.Our pharmaceutical manufacturing site in Delaware City, Delaware is seeking a Quality Manager to join our growing team.Position SummaryThe Quality Manager is responsible for ensuring compliance with quality systems, regulatory requirements, and continuous improvement initiatives.This role maintains a strong presence on the manufacturing floor, leading the development and execution of systems that prevent deviations and ensure consistent product quality.The Quality Manager ensures all packaging materials meet customer expectations and comply with cGMP and regulatory standards, supporting business growth within the pharmaceutical sector.Key ResponsibilitiesLead and execute quality strategy aligned with company and customer expectationsOversee day-to-day quality operations, ensuring compliance with cGMP, FDA, and ISO standardsMaintain a strong floor presence to monitor, review, and improve quality systems and processesLead investigations into deviations, complaints, and nonconformances; implement effective CAPAEnsure timely review and release of batch records, test results, and finished materialsDevelop, maintain, and continuously improve SOPs, policies, and quality systemsDrive initiatives to reduce defects, complaints, and process variabilityMentor, develop, and manage Quality team performance and training programsEnsure laboratory and testing practices meet global pharmaceutical standardsPartner cross-functionally to support regulatory compliance and operational excellenceMinimum QualificationsBachelor's degree in Science, Pharmacy, or related field7+ years of experience in pharmaceutical or biotech manufacturing within QualityStrong knowledge of cGMP, FDA regulations, ISO standards, and CFR requirementsProven ability to manage multiple priorities and meet critical timelinesExcellent written and verbal communication skillsDemonstrated leadership experience with team development and performance managementProficiency in Microsoft Office (Excel, Word, Project)Preferred QualificationsCertified Quality Engineer (CQE) or equivalent certificationExperience with Lean Manufacturing and/or Six Sigma methodologiesTrack record of driving cost savings and scrap reduction initiativesExperience in a multi-site or global manufacturing environmentAdditional RequirementsBackground check requiredDrug screening requiredEqual Opportunity EmployerLiveo Research is an equal opportunity employer and considers all applicants without regard to race, color, religion, sex, national origin, age, disability, veteran status, genetic information, or any other legally protected characteristic.Compensation details: 85000-140000 Yearly SalaryPI75393dadcd9d-37344-40231686