Project Engineer, Product Transfer at Stryker

Gurugram, Haryana, India

Stryker Logo
Not SpecifiedCompensation
Junior (1 to 2 years), Mid-level (3 to 4 years)Experience Level
Full TimeJob Type
UnknownVisa
Medical Devices, ManufacturingIndustries

Requirements

  • Honors Bachelor’s degree in Engineering or Science fields or equivalency
  • 3+ years of experience in manufacturing environment or equivalent
  • Basic knowledge of GMP, ISO 13485, 21 CFR Part 820 standards
  • Good communication skills
  • Willing to travel in support of business needs to different geographical locations (10% travel)
  • 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 knowledge of manufacturing processes like welding, molding, machining, etc
  • Good hands-on experience of PFMEA & Control Plan
  • 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

Responsibilities

  • Support the implementation of process improvements to Corporate/Site/Division Supplier Initiated Change Request (SICR) procedures and processes
  • Serve as owner, execute, and maintain the electronic systems related to SICRs, and support data alignment (SICR Database & OnePLM SICR Library)
  • Challenge suppliers' SICR forms for completeness and accuracy; discuss corrections to ensure smooth assignment and execution of the change
  • Own & execute Supplier Initiated Change Requests (SICRs) 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)

Skills

SICR
OnePLM
PPAP
MSA
SPC
IQ
OQ
PQ
PFMEA
Control Plan
GMP
ISO 13485
21 CFR Part 820
ECR
ECN
continuous improvement

Stryker

Develops and manufactures medical devices and equipment

About Stryker

Stryker develops and manufactures medical devices and equipment aimed at improving patient care and surgical efficiency. Their products include surgical tools, neurotechnology devices, and orthopedic implants, which are sold directly to hospitals and clinics. Stryker stands out from competitors by focusing on high-quality products and a commitment to advancing healthcare solutions. The company's goal is to enhance the overall healthcare experience for both patients and medical professionals.

Kalamazoo, MichiganHeadquarters
1941Year Founded
$423.3MTotal Funding
IPOCompany Stage
Biotechnology, HealthcareIndustries
10,001+Employees

Benefits

Medical & prescription plans
Supplemental health benefits
Flexible Spending accounts
Employee Assistance Program
Short-term & long-term disability
Tuition reimbursement
401(k) plan
Employee Stock Purchase Plan

Risks

Integration challenges from acquisitions may strain Stryker's resources.
Rapid tech advancements risk obsolescence of Stryker's current products.
Regulatory scrutiny on acquisitions could delay Stryker's market entry.

Differentiation

Stryker's acquisitions enhance its minimally invasive surgical solutions portfolio.
Entry into the peripheral vascular segment diversifies Stryker's market presence.
Stryker's focus on AI integration boosts diagnostic accuracy and operational efficiency.

Upsides

Growing demand for minimally invasive solutions aligns with Stryker's strategic acquisitions.
The orthopedic implants market growth benefits Stryker's expanding product line.
Stryker's acquisition of Inari Medical positions it in a high-growth vascular market.

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