Manager, R&d Verification & Validation (v&v) & Lab Ops

Johnson & Johnson

Irvine, California, United States
Base: $117,000.00 - $201,250.00; bonus/equity: not...
Onsite
Verification and validation (v&v)
Laboratory operations management
Medical device development
The Manager, R&D Verification & Validation (V&V) and Laboratory Operations leads V&V of ophthalmic devices and manages day-to-day lab and compliance activities

Job Summary

  • The Manager, R&D Verification & Validation (V&V) and Laboratory Operations leads V&V of ophthalmic devices and manages day-to-day lab and compliance activities.
  • This position requires technical and leadership skills to advance the development of medical devices before and during V&V activities, acting as the advisor to resolve technical or operational problems.
  • Responsibilities include managing the R&D lab equipment, safety regulations, equipment calibration, internal/external audits, and mentoring/developing a multidisciplinary team.

Matching Summary

The Manager, R&D Verification & Validation (V&V) and Laboratory Operations leads V&V of ophthalmic devices and manages day-to-day lab and compliance activities.

Salary

Base: $117,000.00 - $201,250.00; Bonus/Equity: Not specified; Benefits: Vacation –120 hours per calendar year, Sick time - 40 hours per calendar year, Holiday pay –13 days per calendar year, Work, Personal and Family Time - up to 40 hours per calendar year, Parental Leave – 480 hours, Bereavement Leave – 240 hours for immediate family member, Caregiver Leave – 80 hours, Volunteer Leave – 32 hours, Military Spouse Time-Off – 80 hours

Skills & Requirements

Must-have

  • Verification and Validation (V&V)
  • Laboratory Operations Management
  • Medical Device Development
  • Quality System Regulations
  • Test Planning and Execution

Nice-to-have

  • Inclusive Leadership
  • Test Automation Initiatives
  • Credo-based Decision-making
  • Cross-functional Collaboration

Key Requirements

  • Bachelor’s Degree in engineering
  • 10+ years of medical device test, V&V, and/or QA experience
  • 2+ years of direct people management experience
  • Experience managing V&V teams in Medical Device industry
  • Understanding of design control, requirements management, configuration management, product software V&V, defect management, and software risk analysis
  • Knowledge of ISO 14971, 21 CFR 820
  • Excellent organizational, attention to detail, and multi-tasking skills
  • Outstanding communication and presentation abilities
  • Experience in project management, scheduling, tasking, and budgeting

Work Rights

Not specified

Tailored Resume

Cover Letter