Quality Engineer, DePuy Synthes
Job in
Palm Beach Gardens, Palm Beach County, Florida, 33418, USA
Listed on 2026-06-11
Listing for:
Johnson & Johnson
Full Time
position Listed on 2026-06-11
Job specializations:
-
Engineering
Quality Engineering, Process Engineer, Manufacturing Engineer
Job Description & How to Apply Below
more at
As guided by Our Credo, Johnson & Johnson is responsible to our employees who work with us throughout the world. We provide an inclusive work environment where each person is considered as an individual. At Johnson & Johnson, we respect the diversity and dignity of our employees and recognize their merit.
Job Function:
Supply Chain Engineering
Job Sub Function:
Quality Engineering
Job Category:
Scientific/Technology
All Job Posting Locations:
Palm Beach Gardens, Florida, United States of America
Job Description:
We are searching for the best talent for Quality Engineer to join our DePuy Synthes Quality organization located in Palm Beach Gardens, FL.
The Johnson & Johnson Medical Devices Companies have been working to make surgery better for more than a century. With substantial breadth and depth in surgical technologies, orthopedic and interventional solutions, we aspire to improve and enhance medical care for people worldwide. Together, we are working to shape the future of health through differentiated products and services.
Our rapidly growing Velys Enabling Tech Operation is in need of a Quality Engineer who provides overall quality assurance leadership of on-site manufacturing areas. Ensures manufacturing areas are meeting good manufacturing practices, international organization for standardization and any other applicable standards. This position is focused on the support of New Product Introduction and Value Improvement projects implementation to the PBG Site.
Key Responsibilities
* Provides comprehensive quality support for daily manufacturing activity.
* Manages the initiation, containment, investigation, disposition and closure of Non-Conformances in the PBG and WPB MAKE Sites.
* Performs and/or supports CAPA records, including risk assessment, root cause investigation, corrective and preventive actions and effectiveness monitoring.
* Utilizes industry and process excellence standards on a moderately complex level in daily quality operations, including good manufacturing practices (GMP), equipment engineering system (EES), and international organization for standardization (ISO).
* Addresses or escalates product and process complaints.
* Evaluates contract manufacturer performance metrics and supports management reviews.
* Conducts audits of all quality system categories to assess compliance to process excellence standards.
* Implements comprehensive measurement systems to monitor effectiveness of quality and reliability systems to identify, bracket, correct and prevent defects, demonstrating continuous improvement to man.
* Facilitates technical issues for manufacturing processes that are to be transferred to satellite facilities.
Qualifications
Education:
* A minimum of a Bachelor's degree is required. Degrees in Engineering, Life Science, or related field is preferred.
Experience and Skills:
Required:
* A minimum of 1-2 years of relevant work experience or internships.
* Experience working in regulated industries
* This position will require relevant experience working in manufacturing/operations.
* In-depth knowledge of product/process Risk Management (MDSAP, MDD, MDR, FDA and ISO standards)
* Experience and a proven track record of implementing appropriate risk mitigation
Preferred:
* Advanced knowledge of Six Sigma methodologies.
* Understanding of the NPI (New Product Introduction) process
Other:
* This position will require less than 10% travel
Johnson & Johnson announced plans to separate our Orthopaedics business to establish a standalone orthopaedics company, operating as DePuy Synthes. The process of the planned separation is anticipated to be completed within 18 to 24 months, subject to legal…
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