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Location
In office (Gurgaon)
Seniority
Middle · 3+ years exp
Employment
Full-Time
Overview
Company
Impact
Profile match
Stryker is an American medical technology company founded in 1941 by an orthopaedic surgeon who began manufacturing the mobility devices he had designed for his own patients. It sells hip and knee implants, trauma and extremity fixation, spinal implants, surgical power tools and navigation, hospital beds and stretchers, emergency response equipment, and the Mako robotic arm used for joint replacement planning and execution. Headquartered in Kalamazoo, Michigan and listed on the New York Stock Exchange, it has grown through a steady stream of acquisitions and is one of the largest orthopaedic device makers in the world.
Work Flexibility: Hybrid

What you will do:

  • Support the implementation of process improvements to Corporate/Site/Division Supplier Initiated Change Request procedures and process.

  • Served as owner, execute, and maintain the electronic systems related to SICRs, and support data alignment (SICR Database & OnePLM SICR Library)

  • Challenge suppliers SICRs forms for completeness and accuracy. Discuss corrections to the form to guarantee a smooth assignment and execution of the change.

  • Own & Execute Supplier Initiated change request (SICR) submitted by Global Suppliers

  • Review Submitted SICRs and challenge suppliers for missing information & required deliverables for approving the change

  • Organize SCRB with Key Stakeholders and get Buy in for Type of change.

  • Review and Approve deliverables submitted by suppliers and coordinate with supplier for any corrections.

  • Execute ECR/ECNs and Promotion requests in OnePLM for Change Approval at Stryker end.

  • Support communication tools to internal and external customers (suppliers/site/division)

  • Monitor and Maintain SICR KPIs.

  • Support Global SICR Initiatives

What you will need:

Required Qualification:

  • Honors Bachelor’s degree in Engineering or Science fields or equivalency.

  • 3+ years of experience in manufacturing environment or equivalent.

  • Basic knowledge with GMP, ISO 13485, 21 CFR Part 820 standards

  • Good communication skills.

  • Willing to travel in support of business needs to different geographical locations.

  • Good knowledge of continuous improvement methodologies

  • Hands on experience of PPAP ,MSA, SPC documentation creation, review and Approval from suppliers.

  • Good Hands on experience of Validation activity - IQ,OQ & PQ

  • Good Know how of Manufacturing processes like welding, Molding, Machining etc.

  • Good Hands on experience of PFMEA & Control Plan

Preferred Qualification:

  • Must enjoy working in a team environment

  • Must demonstrate good collaboration and communication skills.

  • Highly motivated and able to build relationships internally and externally.

  • Must demonstrate multitasking skills as this individual will be responsible for multiple tasks at the same time.

  • The individual should enjoy working in a dynamic and results-oriented team environment focusing on quality, compliance and customer satisfaction

Travel Percentage: 10%
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