Senior Quality Engineer

Tata Consultancy Services Ltd

  • Santa Clara, CA
  • 30+ days ago
  • $120,000–$140,000 Per Year

Highlights

Strong expertise in design transfer activities, including DHF DMR transition and compliance with FDA 21 CFR 820 & ISO 13485. Experienced in leveraging advanced statistical methods for reliability prediction and data driven decision making.

Numbers & Facts

LocationSanta Clara, CA
Salary$120,000–$140,000 Per Year

Description

Must Have Technical/Functional Skills

  • Strong understanding of Medical Device Quality Systems and regulatory compliance requirements
  • Working knowledge of ISO 13485:2016/2019 and 21 CFR Part 820 (FDA Quality System Regulation)
  • Strong expertise in design transfer activities, including DHF DMR transition and compliance with FDA 21 CFR 820 & ISO 13485
  • Sound knowledge of Medical Device Regulations, including MDD and MDR
  • Proven experience in Non Conformance (NC) management, CAPA processes, and internal/external audits
  • Expertise in Medical Device Risk Management, with the ability to identify both apparent and less obvious risks
  • Practical experience with Application, Process, Design, and System FMEA methodologies
  • Proficient in statistical tools and techniques, including Design of Experiments (DOE)
  • Capable of performing advanced descriptive and non parametric statistical analyses
  • Experienced in leveraging advanced statistical methods for reliability prediction and data driven decision making

Roles & Responsibilities

  • Lead design transfer and production support activities, ensuring compliance with FDA/ISO 13485 and alignment with manufacturing readiness.
  • Own multiple subassemblies for a surgical robotics platform, ensuring design integrity, quality, and manufacturability.
  • Investigate non-conformances (NCs) using root cause analysis and drive CAPA within the QMS framework.
  • Develop and maintain FMEAs, support risk mitigation, and lead manufacturing issue resolution and qualifications (IQ/OQ/PQ).
  • Identify and implement compliant, alternative solutions to engineering and production challenges while driving continuous improvement.
  • Support and maintain Quality Management System (QMS) processes in compliance with regulatory requirements
  • Collaborate with cross functional teams to deliver quality compliant outcomes
  • Interpret and apply medical device regulations and standards to projects and processes
  • Support audits and regulatory inspections, ensuring timely closure of actions

Salary Range: $120,000- $140,000 a year

TCS Employee Benefits Summary:

Discretionary Annual Incentive.

Comprehensive Medical Coverage: Medical & Health, Dental & Vision, Disability Planning & Insurance, Pet Insurance Plans.

Family Support: Maternal & Parental Leaves.

Insurance Options: Auto & Home Insurance, Identity Theft Protection.

Convenience & Professional Growth: Commuter Benefits & Certificatio n & amp; Training Reimbursement.

Time Off: Vacation, Time Off, Sick Leave & Holidays.

Legal & Financial Assistance: Legal Assistance, 401K Plan, Performance Bonus, College Fund, Student Loan Refinancing.

#LI-SP1

Similar Jobs

See more jobs