Senior Quality Engineer Clean And Pack , Orthopedics

Johnson & Johnson

Raynham, Massachusetts, United States of America
Base: $79,000.00 - $127,650.00; bonus/equity: not ...
Global regulations and standards compliance
Non-conformances capas customer complaints
Material identification segregation
Champions compliance with applicable Global Regulations and standards (e.g. QSRs, ISO, EN and Medical Device Directive (MDD) requirements), including providing support during internal and external audits

Job Summary

  • Champions compliance with applicable Global Regulations and standards (e.g. QSRs, ISO, EN and Medical Device Directive (MDD) requirements), including providing support during internal and external audits.
  • Accountability for material identification, material segregation, classification of defect types including the successful application of these techniques on a day-to-day basis in manufacturing.
  • The anticipated base pay range for this position is : $79,000.00 - $127,650.00

Matching Summary

Champions compliance with applicable Global Regulations and standards (e.g. QSRs, ISO, EN and Medical Device Directive (MDD) requirements), including providing support during internal and external audits.

Salary

Base: $79,000.00 - $127,650.00; Bonus/Equity: Not specified; Benefits: Vacation –120 hours per calendar year Sick time - 40 hours per calendar year; for employees who reside in the State of Colorado –48 hours per calendar year; for employees who reside in the State of Washington –56 hours per calendar year Holiday pay, including Floating Holidays –13 days per calendar year Work, Personal and Family Time - up to 40 hours per calendar year Parental Leave – 480 hours within one year of the birth/adoption/foster care of a child Bereavement Leave – 240 hours for an immediate family member: 40 hours for an extended family member per calendar year Caregiver Leave – 80 hours in a 52-week rolling period10 days Volunteer Leave – 32 hours per calendar year Military Spouse Time-Off – 80 hours per calendar year

Skills & Requirements

Must-have

  • Global Regulations and standards compliance
  • Non-conformances CAPAs customer complaints
  • Material identification segregation
  • Process validation risk management
  • Statistical analysis interpretation

Nice-to-have

  • Act with speed flexibility accountability
  • Understand own work impacts enterprise
  • Lead priorities effectively deliver results

Key Requirements

  • Bachelors or equivalent university degree
  • 2-4 years relevant professional work experience
  • Medical Devices industry experience
  • ISO 13485 FDA QSR knowledge
  • CAPAs non-conformances audits process validation experience

Work Rights

Not specified

Tailored Resume

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