Johnson & Johnson Consumer Inc - Material Quality Lead - Skillman, New Jersey
DescriptionAny additional information you require for this job can be found in the below text Make sure to read thoroughly, then apply.Kenvue is currently recruiting for:Material Quality LeadThis position reports to the Manager, Material Quality and is based at Summit, NJ.Who we areAt Kenvue, we realize the extraordinary power of everyday care. Built on over a century of heritage and rooted in science, we're the house of iconic brands - including Neutrogena, Aveeno, Tylenol, Listerine, Johnson's and BAND-AID Brand Adhesive Bandages that you already know and love. Our global team is made up of 22,000 diverse and brilliant people, passionate about insights, innovation and committed to delivering the best products to our customers. Join us in shaping our future-and yours.Role reports to: Manager, Material QualityLocation: Summit, NJTravel %: 20What you will doThe Materials Quality Lead is responsible for the successful development and implementation of the Supplier Quality Management (SQM) strategy and associated policies, procedures, programs, and initiatives that deliver quality, compliance, material reliability, and/or operating benefit to the supply chain. The Materials Quality Lead actively partners with stakeholders, teams, and external suppliers to implement innovative solutions and continuous improvements with demonstrated and measurable business results.The suppliers and materials managed are utilized in products of multiple regulatory classifications (Drug Products, Cosmetics, NDAs, Class I Medical Devices, Nutritional Products, and Combination Products) and may include Chemicals, APIs, Packaging, and/or Fiber/Non-Wovens. The Materials Quality Lead ensures compliance with processes, controls, and standards for supplier and material quality management, following Kenvue policies and relevant regulations (e.g., 21 CFR 210 & 211, 21 CFR 820, and 21 CFR Part 11, EFfCI, and ICH Q7). As an integral member of project teams, the Materials Quality Lead ensures compliance and quality requirements are met for new and modified raw materials and packaging components.Key Responsibilities
Material Quality Lifecycle Management:Responsible for the Quality review and approval of raw material and packaging change controls. Acts as the Quality SME for material change controls and specifications through engagement with Kenvue Quality teams, Kenvue technical functions (Raw Material Center, Packaging Material Center, Analytical), Procurement, Suppliers, and/or others. Participates in the development of change control strategies for individual material changes and project related strategies for new materials and changes to existing materials.Material Quality Regional Strategy and Deployment:Integrates MQ activities within Supplier Quality's regional objectives in support of improving material and supplier reliability. Partners closely with Kenvue manufacturing sites to identify supplier/material issues impacting performance. Develops material quality strategies to ensure appropriate Critical to Quality/Critical to Process attributes are defined within specifications, or other relevant documents.Material Quality Subject Matter Expert:Support the Raw Material and Packaging centers of excellence, providing the Voice of Quality for material selection, qualification, specifications, and controls.Regional Supplier Quality activities:Performs other activities in support of regional Supplier Quality objectives. Acts as an independent reviewer or approver of non-conformance or other documentation. May be trained as a qualified auditor, to assist in the assessment of supplier performance.What we are looking forRequired Qualifications:A minimum of a Bachelor's degree in a technical field (Engineering, Sciences, or similar disciplines) is required.A minimum of 5 years of GMP experience in either Pharmaceutical, Medical Device Manufacturing, OTC Drug, Cosmetic, and/or Food and Dietary Supplements production.Experience in a Technical or Quality Assurance function is required.Desired Qualifications:Knowledge of GMP requirements (21 CFR parts 210/211 or 820) and current FDA enforcement regulations is required.Participate in cross-functional teams, build collaborative relationships with key stakeholders, timely escalation of issues/roadblocks to management.Demonstrated ability to assess/mitigate risk and manage complex issues autonomously.Knowledge of the principles and practices of quality assurance in the consumer health, pharmaceutical, or medical device industry is required.Experience with Supplier Quality & Change Management is preferred.What's in it for you:Competitive Total Rewards Package*Paid Company Holidays, Paid Vacation, Volunteer Time & More!Learning & Development OpportunitiesEmployee Resource GroupsEqual Opportunity Employer - minorities/females/veterans/individuals with disabilities/sexual orientation/gender identity#J-18808-Ljbffr
