Process Quality Engineer

Process Quality Engineer The Process Quality Engineer is responsible for facilitating a state of high‑quality performance, compliance, and critical oversight/performance monitoring of Philips manufacturing processes, driving compliance and continuous improvement throughout the manufacturing process. Your role: Facilitate operations performance monitoring, reporting, improvement and development, facilitate improvement programs in factory, and support analytical testing and Supplier Quality Engineering (SQE) and purchasing. Conducts assessment of impact to Process Failure Mode and Effects Analysis (PFMEA) and associated controls in relation to design changes and assists in Manufacturing Process Development and Design Transfer activities. Handles nonconformance events/investigations in the factory, guides material review board activities for non‑conformance disposition management, leads analysis of defects for determining dispositions of nonconformances, drives management of Non‑Conformances (NC) and Quality Notifications (QN) and facilitates implementation of effective Corrective and Preventive Actions (CAPA) actions. Facilitates timely quality engineering and quality assurance tasks, ensures manufacturing quality systems are maintained, handles single or complex process validation and process improvement activities, and helps in completion of New Product Introduction (NPI) and product transfers in factory. Possesses working knowledge of Quality Engineering and Continuous Improvement techniques, follows processes and operational policies in selecting methods for obtaining solutions, and frequently interacts with supervisors and functional peer groups to gain cooperation of others. Acts as an advisor to meet schedules and/or solve technical problems, develops and administers schedules and performance requirements, and may have budget responsibilities. Cultivates effective relationships, demonstrates full understanding of area of specialization, demonstrates good working relationships with suppliers, and has previous experience of participation in several New Product Introductions (NPIs). Leads validation protocols, facilitates production builds to support validation activities, analyzes data for reports, process improvement initiatives, and validation activities. Utilizes advanced statistical analysis methods to interpret complex data trends, resolves a wide range of moderate‑complexity requests, and provides strategic insights for continuous enhancement of quality standards and process efficiency. Discusses detailed, strategic quality metrics and reports with stakeholders, highlighting significant achievements, emerging trends, and actionable insights to drive advanced improvement initiatives and ensure regulatory compliance. Delivers specialized advanced training programs on cutting‑edge quality standards, advanced methodologies, and best practices, fostering alignment across functions and advancing excellence in operational practices at an expert proficiency level. Manages environmental monitoring programs (viable and non‑viable) including data analysis and trending, and supports sterilization, endotoxin process analysis to ensure compliance with regulatory and quality requirements. Evaluates equipment control processes, including calibration and maintenance, to ensure compliance with quality and regulatory requirements. You're the right fit if: You have a minimum of 5+ years’ experience in FDA regulated (ISO 13485) medical device quality operations/manufacturing environments, with a focus on quality operations, audit support, process validation/improvement, CAPA, non‑conformance, PFMEA’s and Change/Risk Management (ISO 14971). You have proven experience leading cross‑functional teams and the ability to mentor less experienced engineers. You have detailed experience/knowledge in CAPA processes non‑conformances, including problem identification, root cause analysis, implementation of solutions to prevent recurrence and drive continuous improvement. You’re experienced in utilizing Quality, Reliability and Post Market Surveillance (PMS) insights/data analytics to lead continuous improvement throughout all stages of the product lifecycle. You’re able to build/cultivate relationships with supervisors, functional peer groups, internal/external stakeholders, suppliers etc. Previous experience in environmental control programs and sterilization validation. You have a minimum of a Bachelor’s Degree (Required), in Quality, Engineering or similar disciplines. ASQ‑CQE, ISO Lead Auditor certifications desired. You must be able to successfully perform the following minimum Physical, Cognitive and Environmental job requirements with or without accommodation for this position. How we work together: We believe that we are better together than a part. For our Office‑based teams, this means working in‑person at least 3 days per week. Onsite roles require full‑time (5 days per week) presence in the company’s facilities. Field roles are most effectively done outside of the company’s main facilities, generally at the customers’ or suppliers’ locations. This is an ON‑SITE role. Benefits Generous PTO 401(k) up to 7% match HSA with company contribution Stock purchase plan Education reimbursement Philips Transparency Details: The pay range for this position in Bedford, MA is $102,480 to $163,968. Additional Information: US work authorization is a precondition of employment. the company will not consider candidates who require sponsorship for a work‑authorized visa, now or in the future. Company relocation benefits WILL NOT be provided for this position. For this position, you must reside in or within commuting distance to Bedford, MA. May require travel up to 10%. Equal Employment Opportunity Statement Philips is an Equal Employment and Opportunity Employer including Disability/Vets and maintains a drug‑free workplace. #J-18808-Ljbffr Philips Iberica SAU