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Saint Gobain Performance Plastics Senior Quality Engineer - Manufacturing, Life Sciences - Akron, OH in Akron, Ohio

Why do we need you ? If you want to reshape the world and discover your greatest potential, Saint-Gobain provides one-of-a-kind opportunities for innovative problem solvers. We're one of only two companies in the world that is consistently recognized as both a top Global Employer and a Top 100 Global Innovator, but Saint-Gobain's remarkable story and culture of innovation begins with a team of nearly 200,000 creative, diverse and passionate team members collaborating across the globe. We are committed to our mission to improve lives because, every day, we witness the enormous impact of our efforts on the world around us. The Senior Quality Engineer (SQE) will serve as the immediate delegate to the Quality Manager. The SQE will ensure that the quality standards of the company remain maintained within the SG ICS Akron procedures, policies, purchased components and manufactured products. The SQE will participate in and lead complaint investigations, CAPA investigations, lead supplier audits, drive supplier quality, conduct internal audits and drive continuous improvement projects throughout the plant. The SQE will support and may lead software validations, equipment qualifications and / or process validations required to support existing / new processes. The SQE will participate in and host third party audits and conduct training when needed. Implementation, maintenance, and control of systems & practices, which monitor, assess, and approve the quality of materials and products at all stages of production. Responsible for implementing, maintaining, and facilitating continuous quality improvement objectives, primarily ISO 9001 for the manufacturing location, Saint-Gobain Akron. Ensure the plant remains in full compliance with regulatory requirements and ISO requirements as they pertain to the plant, customer specifications, and corporate quality policies. Key Accountabilities * Lead resolution of internal and external quality issues such as inquiries, quality events, SCARs, complaints, nonconformance's, CAPAs, audits utilizing sound problem solving methodologies. Ensure robust root cause analysis investigation and CAPA for deviations and nonconforming product. * Oversee Quality Review of batch documentation and testing and determine disposition for production batches and incoming raw materials. Acts as liaison between production floor and supply chain for problem resolution and batch documentation scheduling to ensure on time delivery to customer. * Project Management * Supplier Quality * Validation Activities * Customer Management including facilitate/host customer audits. Satisfy customer requests and complete the associated documentation * Conducts training, coordinates functions, resolves issues/problems, and manages projects requiring direction of others throughout the facility as needed. Is this job for you ? Education: Bachelor's degree in Life Sciences or Engineering - REQUIRED Master's in Engineering or Sciences - PREFERRED License/Certification: WCM Greenbelt or equivalent- PREFERRED ASQ certifications (CQE, CQM, CQA) - PREFERRED] Work Experience: 5+ years of experience working in a lead supplier quality role - REQUIRED 10+ years experience Work experience within a manufacturing environment (ISO Cert)-REQUIRED General Skills/Competencies Required: Strong knowledge of ISO and cGMP requirements and relevant industry standard practices. Must have ability to interpret these regulations to ensure proper implementation in the plant systems. Must have experience in performing risk analysis (e.g. FMEA, FTA, PPAP, Risk Ranking/Filtering) Excellent analytical / problem solving, project management, interpersonal and organizational skills required. Proficient computer skills required including Microsoft Access, Excel and Word. Digital solution development

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