Quality Engineer - Operations - JBL Resources

Quality Engineer, Operations
Location: Wilmington, Delaware

About Our Client:
Our Hiring Company, a best-in-class Medical Device Manufacturer has an opening for a new team member at their facility.  Holding itself to the highest standards of integrity, quality and excellence, this company has contributed to the healthcare industry for over 90 years and has been rated as Forbes top 14 most innovative companies in the world. With a strong vision for making medical treatments easier on its patients, this company gears its technological innovations from its top-talented engineers towards making a significant contribution to our society.

Key Responsibilities:

• Proactively investigating, identifying, and implementing best-in-class quality engineering practices.  
• Providing focused quality engineering support and assuming responsibility for timely and effective coordination and execution of assigned development project activities.  
• Establishing effective corrective action plans and leading in implementing quality assurance plans, process controls, and CAPA systems designed to meet or exceed internal and external requirements.  
• Acting as an effective leader or team member in supporting quality disciplines, decisions, and practices.  
• Applying sound, systematic problem-solving methodologies in identifying, prioritizing, communicating, and resolving quality issues.  
• Reviewing and approving product and process qualifications, validations, and other change control-related documentation.
• Developing product/process assurance plans, which include all required elements, and identifying and implementing effective process control systems to support the development, qualification, and ongoing manufacturing of products.  
• Generating internal quality documentation such as quality plans, standard operating procedures, and inspection procedures.  
• Participating in product review boards, identifying non-conformance trends, and developing technical investigation plans, including investigating and analyzing customer/internal complaints.  
• Performing analytical measurements and experiments to qualify or resolve product and process issues.  
• Developing and implementing strategic quality plans, master validation plans, validation protocols, inspection plans, and quality/regulatory compliance operating procedures to meet FDA and ISO requirements.  
• Tracking quality trends and initiating action items to resolve issues while managing assigned corrective actions.  
• Monitoring field quality and analyzing field returns to determine root causes.  
• Providing training and support for quality system processes and quality engineering practices.  

Qualifications: 

• A bachelor’s degree (minimum) in engineering, life sciences, or a related field.
• 3 to 10 years of progressively responsible experience in medical device quality assurance.
• One to two years of auditing experience is preferred.
• Certification as a CQA, CQE, or CQM and membership with ASQ are highly desirable.
• Advanced computer skills to efficiently utilize quality systems and tools.
• Strong writing, mathematical, and statistical skills for data-driven decision-making.
• Adept at managing multiple projects and meeting deadlines with precision.
• Proficient in verbal and written communication to effectively convey complex information.

Interested Candidates please apply on our website at https://jobs.jblresources.com. 
For more information about our services and great opportunities at JBL Resources, please visit our website: https://www.jblresources.com. 
JBL Resources is proud to have earned the reputation of being a premier provider of top talent professionals in the fields of engineering, human resources, logistics, operations, and supply chain management. As specialists in both permanent placement and contract services, our mission is to help companies and individuals become all they were created to be.
**JBL is an Equal Opportunity Employer and E-Verify Company