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Zimmer Biomet is seeking a quality-focused professional to support day-to-day operations, NCRs, CAPA development and implementation, and calibration activities in a GMP environment. The role emphasizes adherence to SOPs and internal/external regulations to ensure quality and compliance.
You will participate in special projects, deliver trainings, and assist with CI initiatives while maintaining rigorous documentation practices and GD&T knowledge.
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. To support our talent team, we focus on development opportunities, robust employee resource groups (ERGs), a flexible working environment, location specific competitive total rewards, wellness incentives and a culture of recognition and performance awards. We are committed to creating an environment where every team member feels included, respected, empowered and recognised.
In this role you will work with the quality engineers supporting day to day operations, Non Conformance Reports-(NCRs), Out of Tolerance Gage Reports, Customer Complaints, Corrective and Preventive Action- (CAPA) development and implementation, Operational Procedures revisions and Continuous Improvement (CI) initiatives. You will have the chance to actively support and participate in special projects. A key part of this role will be the strict observance of company’s procedures, GMP’s, SOP’s and other internal and external requirements or regulations.
Less than 5%
Expected Compensation: $63,000-$79,000 base salary, plus performance bonuses
EOE/M/F/Vet/Disability