Hiring: Quality Manager, Consumer Health Products Company: ZEISS Group Location: Hebron, KY Job Posted Time: 2026-09-16 18:04:01 Target Skills & Keywords : Quality Assurance About the job Experience: •5+ years of experience in Quality Assurance, Quality Systems, Supplier Quality, Regulatory Affairs, or Compliance within an FDA-regulated industry. •Over 179 years? Required Skills: •How many companies can say they’ve been in business for over 179 years? •ZEISS is looking for a hands-on •Quality Manager to help support and scale our growing regulated consumer health portfolio, including OTC sterile eye drops, dietary supplements, cosmetics, and related products •This role is ideal for a practical quality professional who enjoys building inspection-ready systems, partnering with external manufacturers and 3PLs, and ensuring products move safely and compliantly through warehousing, logistics, and fulfillment networks. •This position provides critical local quality oversight over warehousing, logistics, and fulfillment operations. You will work cross-functionally with Regulatory Affairs, Supplier Quality, Operations, Customer Service, and external partners to translate regulatory expectations into clear procedures, training, and day-to-day execution. •The ideal candidate has strong quality systems experience in GMP Quality, OTC drugs, pharmaceuticals, sterile products, medical devices, dietary supplements, cosmetics, personal care, or regulated consumer health products •Provide direct quality oversight of local warehousing, 3PL partners, distribution processes, transit temperature monitoring, and controlled room temperature (CRT) storage programs. •Ensure quality expectations are clearly defined, documented, and executed across warehousing and distribution operations. Qualifications: •Industry Context: Direct experience in one or more of the following areas: OTC drugs, pharmaceuticals, sterile products, medical devices, dietary supplements, cosmetics, personal care, or regulated consumer health products. •Core QA Competencies: Strong working knowledge of GMP quality systems, including deviations, CAPA, change control, document control, complaints, supplier quality, training, and audit readiness. •Supply Chain/Logistics Exposure: Experience working with external partners such as 3PLs, distributors, warehouses, laboratories, or outsourced manufacturers. •Technical Review: Ability to review technical quality documentation, identify risks and gaps, and drive required follow-up. •Communication: Strong written and verbal communication skills with the ability to translate regulatory and quality expectations into clear procedures, training, and business processes. •Direct experience with OTC drug products, sterile ophthalmic products, controlled room temperature distribution, temperature monitoring, or cold-chain distribution models. •Operational familiarity with 21 CFR 210/211, 21 CFR 111, MoCRA, ISO 22716, or related distribution quality and stability standards. •ASQ CQA, ASQ CQM/OE, RAC, or related professional certification. •RAC (Regulatory Affairs Certification / Training) •CQA (Certified Quality Auditor by ASQ) Compensation: •$119,700 - $149,600 / year Interested candidates, please apply directly through the job posting on company's career page or try via AI auto apply on this platform. Don't miss this opportunity to join a forward-thinking team!