QA Production Manager - 2nd and 3rd Shift
Job Title: QA Production ManagerCompany: ZingLocation: Wharton, NJ (On-site)Employment Type: Direct HireSalary: $70,000 – $80,000 annuallySchedule2nd Shift: 3:00 PM – 11:00 PM3rd Shift: 11:00 PM – 7:00 AMAbout The RoleZing is seeking a QA Production Manager to oversee and maintain Quality Management Systems within a regulated manufacturing environment supporting cosmetics and OTC products. This role is responsible for ensuring quality processes are effectively implemented on the production floor while maintaining compliance with FDA and ISO standards.Key ResponsibilitiesDevelop, implement, and maintain the Quality Management System (QMS)Ensure compliance with cGMP, 21 CFR Parts 210/211, and ISO 22716Maintain and oversee quality documentation including SOPs, deviations, CAPAs, and change controlsEnsure approved changes are properly implemented across production operationsCollaborate cross-functionally with Production, QC, R&D, Regulatory, and Engineering teamsLead and support validation activities and review validation documentationInvestigate deviations, customer complaints, and CAPAsMonitor production floor compliance and conduct GMP walkthroughsManage internal and external audit readiness and responsesTrack KPIs and drive continuous improvement initiativesLead routine quality meetings and ensure accountability for action itemsEnsure SOP training programs are current, implemented, and effectiveRequirementsMinimum of 5 years of Quality Assurance experience within cosmetics and/or OTC drug manufacturingExperience in a contract manufacturing environment preferredStrong knowledge of FDA cGMP (21 CFR 210/211) and ISO 22716Experience with FDA inspections and ISO auditsFamiliarity with ICH guidelines and OTC monograph requirementsExperience supporting production environments and implementing quality processes on the floorStrong analytical, problem-solving, and leadership skillsAbility to manage multiple priorities in a regulated environmentPreferred QualificationsFamiliarity with stability programs, microbiological controls, and risk management tools (ICH Q9)What You’ll BringStrong ownership mindset and ability to drive executionHigh attention to detail and compliance mindsetStrong communication and cross-functional collaboration skillsWork EnvironmentOn-site role based in Wharton, NJManufacturing environment requiring adherence to GMP and hygiene standardsEqual Opportunity EmployerZing Recruiting is an Equal Opportunity Employer. We do not discriminate on the basis of race, color, religion, sex (including pregnancy, sexual orientation, and gender identity), national origin, age, disability, genetic information, or any other protected status under federal, state, or local law. We are committed to fostering a diverse and inclusive workplace.#ZINGZIP#ZINGNJ