Social network you want to login/join with: Supplier Quality Engineer (Fixed Term), Warsaw Location: Warsaw, Poland Job Category: Other EU work permit required: Yes Job Reference: 0d81c5f4909c Job Views: 2 Posted: 28.04.2025 Expiry Date: 12.06.2025 Job Description At Zimmer Biomet, we believe in pushing the boundaries of innovation and driving our mission forward. As a global medical technology leader for nearly 100 years, a patient’s mobility is enhanced by a Zimmer Biomet product or technology every 8 seconds. As a Zimmer Biomet team member, you will share in our commitment to providing mobility and renewed life to people around the world. We focus on development opportunities, employee resource groups (ERGs), flexible working, competitive rewards, wellness incentives, and a culture of recognition. What You Can Expect This is a fixed-term full-time position tied to a global project scheduled to conclude September 2026. The Supplier Quality Engineer ensures the highest quality products for Zimmer Surgical customers. Supports overall Supplier Quality Management. Evaluates new and existing suppliers, resolving issues promptly. Provides supplier qualifications, material qualification, issue resolution, and maintains the approved manufacturer list. Performs supplier audits per compliance requirements. Participates in new product development and process improvement teams, formulates quality policies related to Suppliers. How You'll Create Impact Audits Conducts external system and process audits at suppliers. Performs product, desktop, and qualification audits. Follows up on Supplier Corrective Actions and reports metrics. Ensures compliance with regulatory and corporate requirements. Assists project teams with quality issues. Supplier Quality Engineer Responsibilities Monitors corrective actions related to NCR findings. Assists suppliers in corrective and preventive strategies. Identifies risks related to quality systems and regulatory changes. Analyzes quality metrics and develops reports for KPI and management review. Collaborates with Sourcing on supplier performance and issues. Approves supplier selection through qualification processes. Supports qualification of new parts. Works with Global Supplier Management on supplier changes and new product introductions. Participates in Material Review Board and Supplier Review Board. What Makes You Stand Out Ability to interpret drawings. Knowledge of FDA, ISO 13485, GMP regulations. Experience with standards, auditing, and communication skills. Understanding of engineering and internal processes. Proficiency with MS Office, SAP, MS Project. Strong report writing and analytical skills. Knowledge of production and business processes. Your Background Technical degree or equivalent, with auditor training preferred. Experience in manufacturing, preferably medical devices or pharma. Problem-solving, analytical, and interpersonal skills. Continuous learner. Fluent in English, both spoken and written. Travel Expectations Up to 10%EOE/M/F/Vet/Disability
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