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Gurugram, 122001, IN
Job details
Work flexibility: Hybrid
Req ID: R536317
Employee type: Full Time
Job category: Engineering
Travel: 20%
Relocation: No
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Why join Stryker?
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Job description
What you will do
Primary responsibilities include:
- Liaison between suppliers and Stryker to drive effective continuous improvement to the supply base.
- Works with internal customers and suppliers to support supplier quality issues and provide technical support for activities related to supplier quality system assessment, performance evaluation and quality improvement projects.
- collaborates with the strategic sourcing, auditing and development groups to understand capabilities and competencies of suppliers to fulfill quality and regulatory requirements
- Assess and critique supplier processes and control documentation and drive improvement in the supplier QMS
- Articulate detailed supplier performance results and trends to appropriate levels of management
- Support tracking and reporting of KPI and other metrics associated with supplier performance
- Provide education and training to suppliers, as necessary
- Maintain and track completion of supplier action plans
- Identify and execute cost reduction opportunities through quality improvements at suppliers.
- Transfer “lessons learned” from the supply base back to R&D, AO, RA, and other functions for incorporation into next generation designs
- Participate in cross-functional projects as needed.
What you need
Basic Qualifications:
- B. Eng. in a science, engineering or related discipline preferred, or equivalent years of experience
- 2+ years’ experience in manufacturing environment or equivalent
- Overall, 3-5 years career experience in Supplier Quality roles.
Preferred Qualifications:
- Experience in a highly regulatory environment
- Basic knowledge of FMEA, validation programs and SPC processes
- Basic understanding of manufacturing processes, prints, tolerancing, project management and statistics
- Strong interpersonal skills, written, oral communication and negotiations skills
- Knowledge and understanding of US and International Medical Device Regulations
- Travel required.