Staff Quality Engineer II (Hybrid
At Auctis · Franklin Lakes, NJ, United States
Salary: $126,600 to $130,000
- QA and testing
- Full-time
- Staff or principal
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Where you’ll work
Hybrid, based in the United States
“Franklin Lakes, NJ, United States”
From the location.
“Location: Franklin Lakes, New Jersey, United States Company: Becton, Dickinson, and Company HR: Mable Farish”
From the job description.
“STAFF QUALITY ENGINEER II (HYBRID”
From the job title.
Hybrid means some days in the office. The listing says how many, and where.
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- First seen by us
- 15 October 2026
- Last checked
- 23 hours ago
Job description
From Auctis’s job post, as they wrote it.
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.
Read the full description
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
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