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Stryker

Manufactures orthopedic and surgical medical devices

Project Engineer Product Transfer

Quality EngineeringConfirmed live in the last 24 hours
Full-timeGurugram, Haryana, IndiaNo salary listed

About the Job

Requirements

  • An honors bachelor's degree in Engineering or Science fields, or equivalency.
  • At least 3 years of experience in a manufacturing environment or equivalent.
  • Basic knowledge of Good Manufacturing Practices, ISO 13485, and 21 CFR Part 820 standards.
  • Good communication skills.
  • Willingness to travel to different geographical locations in support of business needs.
  • Good knowledge of continuous improvement methodologies.
  • Hands-on experience creating, reviewing, and approving supplier PPAP, MSA, and SPC documentation.
  • Hands-on experience with validation activities, including IQ, OQ, and PQ.
  • Good knowledge of manufacturing processes such as welding, molding, and machining.
  • Hands-on experience with PFMEA and Control Plans.

Responsibilities

  • Support implementation of process improvements to Corporate, Site, and Division Supplier Initiated Change Request procedures and processes.
  • Own, execute, and maintain the electronic systems related to SICRs, and support data alignment for the SICR Database and OnePLM SICR Library.
  • Challenge suppliers' SICR forms for completeness and accuracy, and discuss corrections to ensure smooth assignment and execution of changes.
  • Own and execute Supplier Initiated Change Requests submitted by global suppliers.
  • Review submitted SICRs and challenge suppliers for missing information and required deliverables for change approval.
  • Organize Supplier Change Review Board meetings with key stakeholders and obtain buy-in for the type of change.
  • Review and approve supplier-submitted deliverables and coordinate corrections with suppliers.
  • Execute ECR/ECNs and promotion requests in OnePLM for change approval at Stryker.
  • Support communication tools for internal and external customers, including suppliers, sites, and divisions.
  • Monitor and maintain SICR KPIs.
  • Support global SICR initiatives.

Desired Qualifications

  • Enjoy working in a team environment.
  • Demonstrate collaboration and communication skills.
  • Be highly motivated and able to build relationships internally and externally.
  • Demonstrate multitasking skills while handling multiple tasks simultaneously.
  • Enjoy working in a dynamic, results-oriented team environment focused on quality, compliance, and customer satisfaction.

About the Company

Stryker

Manufactures orthopedic and surgical medical devices

Stryker makes medical devices for hospitals, surgical centers and emergency responders, spanning joint implants, surgical instruments and patient transport equipment. Its Mako platform assists surgeons with joint replacement, while its neurotechnology products support brain and spine procedures and stroke treatment. Clinicians use its equipment during surgery and emergency care, and the company earns money by selling implants, disposable products and capital equipment through direct sales teams and distributors. The business also supplies training and technical support for healthcare providers using its devices. Stryker was founded in 1941 and is headquartered in Portage, Michigan.

Company size
10,001+
Company stage
IPO
Headquarters
Portage, MI
Founded
1941

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