Quality Engineer - I (Medical Device)

Jabil • West Chester, PA

5d

About The Position

At Jabil we strive to make ANYTHING POSSIBLE and EVERYTHING BETTER. We are proud to be a trusted partner for the world's top brands, offering comprehensive engineering, manufacturing, and supply chain solutions. With over 50 years of experience across industries and a vast network of over 100 sites worldwide, Jabil combines global reach with local expertise to deliver both scalable and customized solutions. Our commitment extends beyond business success as we strive to build sustainable processes that minimize environmental impact and foster vibrant and diverse communities around the globe. How will you make an impact? As a Quality Engineer , you will support key quality systems, ensure compliance with internal and regulatory standards, and provide day-to-day engineering support to manufacturing operations. Your work will drive continuous improvement, enhance customer satisfaction, and contribute directly to product and process excellence.

Requirements

• Bachelor’s degree required; Engineering or related technical field preferred.
• Minimum of 2 years of relevant experience in Quality Engineering or a regulated manufacturing environment.
• Experience in root cause analysis, process validation, and quality systems.
• Strong understanding of quality system regulations and standards.
• Proficient in statistical analysis tools and techniques.
• Excellent written and verbal communication skills.
• Strong decision-making, organizational, and problem-solving abilities.
• Ability to work independently and collaboratively across teams.
• Skilled in using PC-based systems including Microsoft Office and quality management software.

Nice To Haves

• Experience with inspection planning, control plans, and validation in a regulated environment.
• Familiarity with Six Sigma or other structured problem-solving methodologies.
• Prior experience participating in audits or regulatory inspections.
• Working knowledge of complaints handling, document control systems, and inventory management tools.
• Certification in Quality Engineering (e.g., CQE) is a plus.

Responsibilities

• Promote and uphold site safety policies and procedures.
• Support key business metrics by providing Quality Engineering expertise for manufacturing processes.
• Conduct root cause analyses for quality issues using tools such as 8D, A3, and Six Sigma.
• Perform statistical analyses including ANOVA, DOE, Weibull, GR&R, capability studies, FMEA, and TMV.
• Evaluate, design, and implement inspection and process control systems.
• Assist in validation activities for processes, equipment, software, and computerized systems.
• Prepare and maintain clear documentation including protocols, reports, and procedures.
• Support new product introductions and process transfers.
• Participate in complaint investigations, nonconformances, and CAPA activities.
• Collaborate cross-functionally in quality review meetings (e.g., CAC, TIC, MIC, QIC).
• Engage in internal/external audits and regulatory compliance activities.
• Provide training and guidance to manufacturing personnel on quality standards and inspection techniques.
• Lead or support continuous improvement and cost-reduction initiatives.

Benefits

• Medical, Dental, Prescription Drug, and Vision Insurance with HRA and HSA options
• 401K match
• Employee Stock Purchase Plan
• Paid Time Off
• Tuition Reimbursement
• Life, AD&D, and Disability Insurance
• Commuter Benefits
• Employee Assistance Program
• Pet Insurance
• Adoption Assistance
• Annual Base Pay Increase
• Community Volunteer Opportunities

What This Job Offers

• Job Type: Full-time
• Career Level: Entry Level
• Number of Employees: 5,001-10,000 employees