Quality Manager

Overview Embark on an extraordinary journey with us at Innovative Skincare, home of the renowned iS CLINICAL cosmeceutical brand. We are not just about creating groundbreaking skincare products; we are about creating chemistry that extends beyond the lab – a dynamic synergy between our products and our people. At Innovative Skincare, we believe in a unique formula: the perfect blend of professional expertise and cultural harmony. This philosophy fuels our brand’s continuous growth and empowers each member of our team. We are more than a company; we are a community bound by passion, dedication, and a deep love for what we do, crafting an atmosphere that is as vibrant and energizing as our products. Who we are: Discover a world where skincare innovation meets scientific excellence at Innovative Skincare, a globally acclaimed leader in high-performance cosmeceuticals. Our journey is rooted in the relentless pursuit of creating skincare products that are not only effective but transformative. At the heart of our brand is the iS CLINICAL line, renowned for its fusion of nature’s finest ingredients with cutting-edge science. We are driven by a deep understanding of skin biology and a passion for unlocking the secrets of skin health and rejuvenation. Our ethos is built on the pillars of innovation, integrity, and excellence. Our team members at Innovative Skincare are part of a company that is shaping the future of skincare, where your work contributes to the well-being and confidence of people globally. Join us and be a part of this exciting alchemy where your talent meets our vision, creating a world of pure chemistry! Role The Site Quality Manager will serve as the site lead for all quality-related operations, overseeing the implementation, maintenance, and continual improvement of quality systems to ensure all products meet the highest safety, efficacy, and compliance standards. This role will be responsible for the strategic direction and execution of quality operations across the entire site, including Quality Control (QC), Quality Assurance (QA), and compliance functions. Responsibilities Manage the daily operations of the Quality Department, including QC and QA functions. Maintain and improve the company’s Quality Management System (QMS) in accordance with applicable regulations and industry best practices. Serve as the site quality lead, representing the Quality function in cross-functional leadership meetings and strategic planning sessions. Ensure compliance with U.S. FDA (OTC and cosmetic regulations), EU Cosmetics Regulation, and other applicable quality standards. Oversee site-wide compliance with internal policies, regulatory requirements, and industry standards. Ensure site readiness for regulatory inspections, client audits, and internal assessments. Lead site-level risk management activities related to product quality, including risk assessments and mitigation planning. Collaborate with Facilities, Engineering, and EHS to ensure environmental and operational conditions support product quality and regulatory compliance. Drive site-wide quality culture initiatives, promoting ownership of quality across all departments. Monitor and report on site-level quality KPIs, trends, and performance metrics to senior leadership. Support site expansion or transfer projects, ensuring quality systems are appropriately scaled and integrated. Train and mentor staff on quality processes, GMP requirements, and continuous improvement practices. Monitor quality metrics and prepare reports for leadership to track trends and identify improvement opportunities. Support complaint investigations and manage product returns in accordance with established procedures. Champion initiatives to enhance product consistency, reduce defects, and improve manufacturing efficiency. Other duties as assigned. Qualifications Bachelor’s degree in Quality Management, Life Sciences, Engineering, or a related field. 5+ years of quality assurance/quality control experience in cosmetics, OTC, skincare, or related industries. Strong understanding of GMP, FDA, and international quality standards. Experience managing a QMS and leading audits. Demonstrated ability to lead CAPA processes and root cause investigations. Strong organizational skills with attention to detail and accuracy. Excellent communication skills for cross-functional collaboration ASQ (CQE, CQA) certification or equivalent is a plus. Experience with site commissioning, validation, or expansion projects is a plus. Our company is dedicated to providing equal employment opportunities and embraces diversity and inclusion in our workplace. All eligible candidates will be considered for employment without bias towards their race, ethnicity, religion, gender, gender identity or expression, sexual orientation, national origin, genetic information, disability, age, or veteran status. #J-18808-Ljbffr iS CLINICAL