Overview

B. Braun Medical, Inc.Company: B. Braun US Device Manufacturing LLCJob Posting Location: Allentown, Pennsylvania, United StatesFunctional Area: QualityWorking Model: OnsiteDays of Work: Wednesday, Tuesday, Friday, Thursday, MondayShift: 5X8Relocation Available: NoRequisition ID: 8695B. Braun Medical Inc., a leader in infusion therapy and pain management, develops, manufactures, and markets innovative medical products and services to the healthcare industry. Other key product areas include nutrition, pharmacy admixture and compounding, ostomy and wound care, and dialysis. The company is committed to eliminating preventable treatment errors and enhancing patient, clinician and environmental safety. B. Braun Medical is headquartered in Bethlehem, Pa., and is part of the B. Braun Group of Companies in the U.S., which includes B. Braun Interventional Systems, Aesculap and CAPS .Globally, the B. Braun Group of Companies employs more than 64,000 employees in 64 countries. Guided by its Sharing Expertise philosophy, B. Braun continuously exchanges knowledge with customers, partners and clinicians to address the critical issues of improving care and lowering costs. To learn more about B. Braun Medical, visit Position SummaryThe Quality Engineer I provides quality support to ensure compliance, product quality, and continuous improvement. This role leads investigations, CAPAs, complaint trend analysis, risk assessments, and validation activities while partnering with cross-functional teams to resolve quality issues and improve processes. Key Responsibilities Lead root cause investigations for nonconformances, complaints, and quality events.Manage CAPAs, change controls, and quality improvement initiatives.Serve as the Quality representative for Material Review Board (MRB) meetings.Conduct risk assessments and develop mitigation plans to support Quality and Production KPIs.Support equipment qualification, installation, and test method validation activities.Audit manufacturing processes, suppliers, and raw materials to ensure quality standards are met.Collaborate with Engineering, Manufacturing, and Operations teams to identify and mitigate quality risks.Analyze quality data and complaint trends to drive continuous improvement. Qualifications RequiredBachelor's degree in Engineering, Quality, Life Sciences, or a related technical field.2+ years of experience in Quality Engineering, Quality Assurance, Manufacturing, or a related field.Experience with root cause analysis, investigations, and CAPA management.Strong analytical, problem-solving, and communication skills.Preferred Experience in a regulated industry (medical device, pharmaceutical, or manufacturing).Experience with root cause analysis, nonconformance, and change control processes.ASQ, Six Sigma, or other quality-related certifications.Knowledge & Skills Quality systems and regulatory compliance.Risk management and continuous improvement methodologies.Ability to manage multiple priorities and work effectively across functions.Strong technical writing and documentation skills.Additional Information Occasional travel may be required.Ability to work in both office and manufacturing environments.Must be able to occasionally lift up to 20 pounds.Why Join Us?Join a collaborative team where you'll have the opportunity to solve complex quality challenges, drive continuous improvement, and make a direct impact on product quality and customer satisfaction. Salary Range: $85,300 - $95,300The targeted range for this role takes into account a range of factors that are considered when making compensation and hiring decisions; included but not limited to: skill sets; experience and training; licensure and certifications; and other business and organizational needs. The disclosed range estimate has not been adjusted for the applicable geographic differential associated with the location at which the position may be filled. Compensation decisions are dependent on the facts and circumstances of eac