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STAFF QUALITY ENGINEER II (HYBRID

Auctis Corporation
Franklin, NJ Full Time
POSTED ON 4/13/2025
AVAILABLE BEFORE 5/12/2025

About the job STAFF QUALITY ENGINEER II (HYBRID

Staff Quality Engineer II (Hybrid)

Location : Franklin Lakes, New Jersey, United States Company : Becton, Dickinson, and Company HR : Mable Farish

Base Salary : USD $126,600 to $130,000

Relocation Assistance : Possible for ideal candidate

Required Experience : 10 to 15 years

Minimum Education : Bachelor's Degree

Industry : Medical Equipment / Devices

Job Category : Manufacturing - Quality

Description : Join us at Becton, Dickinson, and Company, a global leader in medical technology. As a Staff Quality Engineer II, you'll play a vital role in our Wearable Injector platform, contributing to new product development and maintenance. Bring your expertise in design control, problem-solving, and analytical skills to ensure product quality through processes like validation, measurement system analysis, root cause analysis, and design verification.

Responsibilities :

  • Evaluate customer requirements and identify quality standards
  • Release products during development activities
  • Implement PS global procedures and standards for QE engineering
  • Support audits and corrective actions
  • Conduct Failure Investigations and problem-solving sessions
  • Approve new design / process specifications
  • Provide guidance to team members
  • Design and perform development independently
  • Liaise with Manufacturing Plants
  • Define product control strategy and lead risk management activities
  • Ensure design control elements are satisfied
  • Perform process validation activities
  • Evaluate test methods and develop systems related to project quality activities
  • Support continuous improvement and customer-facing teams
  • Ensure agreement terms are met
  • Provide technical support from a quality perspective

Position Requirements :

  • Education : BS degree in Engineering or other scientific field
  • Experience : Quality Engineering experience or 12 years in the industry (Medical Device / Pharmaceutical)
  • Special Skills :

  • Thorough understanding of industry regulations / standards : ISO 13485, QSR, GMP
  • Knowledge of design control principles
  • Statistical methods for Quality Assurance
  • Experience in Quality System, Six Sigma Methodology, Validation, FMEA / Risk Management
  • Knowledge and experience in manufacturing, project management, and engineering
  • Good written and oral communication skills
  • Excellent problem-solving and analytical skills
  • Strong leadership capability
  • Ability to handle multiple projects simultaneously in an unsupervised environment
  • Become a maker of possible with us. Advance the world of health. Join BD and unleash your potential.

    Salary : $126,600 - $130,000

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