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Quality Assurance Systems Specialist m/w
Il y a 3 mois
Position Overview
At Zimmer Biomet, we are dedicated to advancing innovation and fulfilling our mission. As a leading global entity in medical technology for nearly a century, a Zimmer Biomet product or technology enhances patient mobility every 8 seconds.
As a member of the Zimmer Biomet team, you will be part of our commitment to delivering mobility and renewed life to individuals worldwide. Our focus on development opportunities, strong employee resource groups (ERGs), a flexible work environment, competitive total rewards tailored to specific locations, wellness incentives, and a culture of recognition and performance awards reflects our dedication to fostering an inclusive, respectful, and empowering workplace.
Key Responsibilities
In the role of Quality Systems Specialist m/w, your primary duty will be to ensure adherence to established regulatory standards through the effective application of Quality Management System principles and processes. Additional responsibilities include:
- Overseeing corporate supplier quality systems projects aimed at developing and implementing processes, procedures, and instructions to maintain and enhance the Supplier Quality Management System.
- Assisting senior management in the strategic planning of quality systems strategies and objectives.
- Leading cross-functional and cross-divisional teams in the formulation and execution of corporate quality systems strategies and objectives.
- Driving corporate quality systems initiatives for the development and implementation of harmonized supplier quality systems and best practices across the organization.
- Identifying and addressing continuous improvement opportunities to enhance the efficiency of Zimmer's quality systems.
- Diagnosing and resolving product, system, and process issues.
- Supporting various teams in conducting audits and assessments of internal processes and supplier manufacturing sites, including CAPA.
Qualifications
The ideal candidate will possess a Bachelor's degree in Engineering, Business Administration, Finance, or a related field, along with 5 to 7 years of experience in Project Management within the Quality/Regulatory Compliance sector. A CQE or equivalent certification is preferred.
Success Factors
- Familiarity with all components of a quality system, including purchasing controls, management responsibility, resource management, product realization, and measurement, analysis, and improvement processes.
- Knowledge of quality assurance techniques such as inspection methods, statistical sampling plans, gauging and test methods concepts, validation, and statistical process control.
- Ability to manage daily operational aspects of Corporate Supplier Quality Systems projects.
- Capability to create and execute project work plans, adapting as necessary to meet evolving needs and requirements.
- Proficiency in applying Quality Systems methodology and enforcing project standards.
- Ability to harmonize and effectively implement best practices for supply chain management, supplier quality, and purchasing controls globally.
- Ensuring project documentation is complete, current, and appropriately stored.
- Demonstrating technical expertise, project management, and time management skills.
- Exhibiting a commitment to continuous improvement.
- Working independently while considering various options for task completion.
- Strong written and verbal communication skills in both French and English.
- Willingness to independently identify, learn, and apply new skills as required.
About Us
VIMS, now part of Zimmer Biomet Holdings, Inc., specializes in the development and commercialization of visualization systems for laparoscopic and arthroscopic procedures, providing fully integrated broadcasting solutions with ultra-high-definition resolution.
EOE/M/F/Vet/Disability
