Supplier Quality Manager

With sales of €700m and 3,300 employees worldwide, Nemera is one of the leading global manufacturers of complex drug delivery systems for the pharmaceutical industry, offering to patients a broad product portfolio which includes inhalation devices, injection devices, nasal and dermal pumps and ophthalmic delivery devices. Nemera has built very long lasting, strong relationships with the leading global pharmaceutical companies globally by providing high quality development, industrialization and manufacturing services. Nemera develops and manufactures its own IP product platforms but also offers also fully custom developments and contract manufacturing. Nemera’s manufacturing sites are located in the US, France, Germany, Brazil and Poland. The headquarters and Innovation Center for early device design and development are located in France (Lyon). We have big ambitions at Nemera! We are growing our franchises and strengthening our capabilities. The Supplier Quality Manager is responsible for planning, coordinating and managing all assigned projects and audits to ensure supplier qualification and routine performance and maintain continuous production and distribution of products consistent with established Quality standards. This role works closely with procurement, engineering, manufacturing, and suppliers to improve product quality and reduce risks in the supply chain. KEY RESPONSIBILITIES/ESSENTIAL FUNCTIONS: Plan, coordinate, and manage Supplier Quality evaluations through scheduling and auditing of suppliers  Interact with suppliers and ensure mutual interpretation of specified requirements to make certain customer requirements and objectives are met  Evaluate compliance using relevant information and individual judgment to determine whether events or processes comply with specifications, operating procedures, or standards  Support implementation and management of quality agreements with all suppliers  Work with Supply Chain and Procurement to evaluate and manage supplier performance  Identify and complete continuous improvement projects utilizing Six Sigma tools and methodologies  Assist the Plant Quality Manager in coordinating and executing objectives throughout the company in cooperation with other managers, to maximize product quality and operating system efficiency and effectiveness to minimize costs  Identify and coordinate resolution of system inefficiencies that contribute to increased quality costs  Utilize CAPA problem solving techniques to reduce internal and external failures, select sound techniques (FMEA, Design of Experiments, Cause and Effect, Flow Charts, SPC) to solve problems effectively, and assess results for application, validity, and conformance to specifications  Analyze supplier quality data and performance metrics Oversee Incoming Inspection process and responsible for managing non-conformities related to supplied materials Assist in maintaining ISO and FDA QMSR quality system compliance  Generate and provide monthly reports  Execute specific responsibilities as defined within the company quality operating system  Support and maintain all policies of the company, including but not limited to applicable FDA regulatory and ISO requirements, Health and Safety Requirements and Continuous Improvement initiatives  Suggest ways to improve the efficiency and safety of our work and environment  Other duties as assigned    POSITION REQUIREMENTS: Bachelor’s Degree in Engineering, Science or related fields required Must have 5 or more years of experience in a Quality position Experience in the Medical Device industry preferred Must have ability to apply advance mathematical concepts and intermediate statistical knowledge Ability to regularly lift up to 40lbs with repetitive movements Ability to push and pull items Ability to stand and/or walk up to constantly during the shift PREFERRED KNOWLEDGE/SKILLS: Formal Quality certification (CQM, CQE) Leadership and good intrapersonal communication skills Six-sigma black belt experience, training, and certification preferred 3+ years of supervisory experience in a similar environment strongly preferred Computer skills including Microsoft Office application and SAP experience Ability to work independently from verbal and/or written instructions Ability to understand and articulate how individual role and responsibilities tie into Quality department objectives WORK ENVIRONMENT Works in a clean manufacturing environment that may include moderate noise levels and required appropriate cleanroom apparel Up to 40% travel required ADDITIONAL NOTES This Job Description is not designed to cover or contain a comprehensive listing of activities, duties or responsibilities that are required of the employee and may be revised at any time by the Company. Why Join Nemera? At Nemera, we prioritize patients when creating drug delivery devices, understanding that accurate dosing and ergonomics are crucial for treatment adherence. Joining Nemera means becoming part of a team that enjoys working together and consistently delivers on its commitments. We take pride in our work because it improves patients’ lives. We look forward to receiving your application (resume submitted in English is appreciated). We offer varied jobs job in an international group, if you want to discover more about Nemera, please look at our website www.nemera.netKnow someone at Nemera? We have a Referral Program so, be sure to have them submit you as a referral prior to applying for this position POSITION RANGE : $100,000- $125,000 USD Salaried  (This is the range that we in good faith believe is the range of possible compensation for this role at the time of this posting. This range may be modified in the future.) For US Benefits, CLICK HERE . Nemera is an equal opportunity employer and does not discriminate against any person on the basis of race, religion, color, gender, gender identity, sexual orientation, age, national origin, disability, veteran status, or any other protected class indication. This company is required by federal law to hire only persons who can establish they are eligible to work in the United States.