Project Engineer, Product Transfer

Posted 9 Days Ago
Be an Early Applicant
Gurugram, Haryana
In-Office
Mid level
Healthtech
The Role
As a Project Engineer, you will manage Supplier Initiated Change Requests by supporting process improvements, reviewing submissions, and coordinating with stakeholders. This role involves hands-on validation activities and supplier communications for manufacturing processes.
Summary Generated by Built In
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)  

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%

Top Skills

21 Cfr Part 820
Gmp
Iso 13485
Msa
Oneplm
Ppap
Spc
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The Company
HQ: Irvine, CA
956 Employees

What We Do

Inari Medical, Inc. is a commercial-stage medical device company focused on developing products to treat and transform the lives of patients suffering from venous diseases.

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