Strategic Supplier Quality Engineer - Medical Devices
$103k - $163kPhilips
Job Description The Supplier Quality Engineer is a key member of Philips’ Image Guided Therapy Devices (IGTD) Quality team, responsible for driving supplier performance and continuous/process improvement, striving for continuous quality improvement throughout the product lifecycle, and ensuring regulatory compliance. Job Title Supplier Quality Engineer Job Description The Supplier Quality Engineer is a key member of Philips’ Image Guided Therapy Devices (IGTD) Quality team, responsible for driving supplier performance and continuous/process improvement, striving for continuous quality improvement throughout the product lifecycle, and ensuring regulatory compliance. Your Role Coordinates and executes supplier improvement initiatives, managing the Approved Supplier List and negotiating Supplier Quality Agreements. Provide sustaining SQE activities in managing daily NCR's, SCAR's, SCN's, and the ASL. Manage APQP with selected suppliers. Facilitates technical capability assessments of potential new suppliers, ensuring they meet the company's quality standards, and contributes to the supplier selection. Proactively monitoring and measuring product/process quality and performance trends and troubleshooting of production/release issues. Assists with the process of making additions, changes, or deletions to the Approved Supplier List, ensuring that only qualified suppliers are retained. Supports in end-to-end performance management of suppliers, conducts detailed analysis of defects to determine if they are supplier-caused, and acts as an independent reviewer for Supplier Corrective Action Requests. Proactively monitoring and measuring product/process quality and performance trends and troubleshooting of production/release issues. Develop and oversee equipment qualification and process validation plans and lead continuous improvement projects based on process/product trends, customer complaints, industry standards and government regulations. Provide Quality oversight of product/process change requests from suppliers, ensuring appropriate regulatory review and adequate validation to support requested changes. Drive supplier improvement, corrective and corrective actions (SCARS). Serve as internal and supplier quality auditor, managing planning, execution, reporting and closure of audits and audit findings. You're The Right Fit If You have a minimum of 5+ years’ experience in Supplier Quality Engineering within FDA regulated medical device environments, with a focus on supplier selection, performance assessment, APQP, Risk Assessments/PFMEA’s, SPC, SCAR’s, SICR, CAPA, Remediation etc. You have detailed knowledge of medical device regulations, requirements, and standards, such as 21 CFR Parts 803, 806, and 820, ISO 13485, ISO 14971, European Medical Device Directive (93/42/EEC), EU Medical Device Regulation, Canadian Medical Devices Regulation (SOR/98-282).You have proven experience utilizing data analytics/KPI’s to assess supplier performance and identify/drive process improvement opportunities. You have strong communications skills and the proven ability to effectively communicate, influence and build relationships cross-functionally with a variety of internal/external stakeholders, suppliers, Regulatory Agencies, Notified Bodies etc. You have a minimum of a Bachelor’s Degree (Required) in Quality, Engineering, or related disciplines. ASQ and/or Six Sigma DfX 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 presence (% days per week) 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 Office-based role. About Philips We are a health technology company. We built our entire company around the belief that every human matters, and we won't stop until everybody, everywhere, has access to the quality of healthcare that we all deserve. Do the work of your life to help improve the lives of others. Learn more about our business. Discover our rich and exciting history. Learn more about our purpose. Learn more about our culture. Philips Transparency Details The pay range for this position in Bedford, MA is $103,000 to $163,000 The actual base pay offered may vary within the posted ranges depending on multiple factors including job-related knowledge/skills, experience, business needs, geographical location, and internal equity. At Philips , it is not typical for an individual to be hired at or near the top end of the range for their role and compensation decisions are dependent upon the facts and circumstances of each case. In addition, other compensation, such as an annual incentive bonus, sales commission or long-term incentives may be offered. Employees are eligible to participate in our comprehensive Philips Total Rewards benefits program, which includes a generous PTO, 401k (up to 7% match), HSA (with company contribution), stock purchase plan, education reimbursement and much more. Details about our benefits can be found here. 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. This role may require travel up to 10%. This requisition is expected to stay active for 45 days but may close earlier if a successful candidate is selected or business necessity dictates. Interested candidates are encouraged to apply as soon as possible to ensure consideration. Philips is an Equal Employment and Opportunity Employer including Disability/Vets and maintains a drug-free workplace. #J-18808-Ljbffr Philips
$115k - $182k
Software Test Engineer - Medical Device Integration (Bedford, MA) Job Description You will join a high... ..., clear, and testable. Support high‑quality delivery by validating requirements... ...facilities, generally at the customers’ or suppliers’ locations. This is an office‑based...SuggestedFull timeWork at officeWork visaRelocation package3 days per week$115k - $182k
**Software Test Engineer - Medical Device Integration (Bedford, MA)** You will join a high-performing... ..., clear, and testable. Supports high-quality delivery by validating requirements... ...facilities, generally at the customers’ or suppliers’ locations.This is an office-based...SuggestedFull timeWork at officeImmediate startWork visaRelocation package3 days per week- Mass Digital Health is seeking a Design Quality Engineer in Bedford, MA. This role entails overseeing the design control process from validation to design transfer, ensuring quality and regulatory compliance. Key responsibilities include developing process validation strategies...Suggested
$145k - $175k
LeMaitre Vascular, a growing NASDAQ medical device company, seeks a Director of Business Development to lead acquisitions and other strategic transactions. The ideal candidate will have a Bachelor's degree (MBA preferred) and at least 5 years of experience in the medical...Suggested$90k - $102k
Elevaris Medical Devices is seeking a Quality Engineer in Wilmington, MA to ensure compliance with medical device regulations and support quality systems. Applicants should have a Bachelor's degree in Engineering, Science, or Math, and 2-4 years of related experience. Key...Suggested- Analog Devices, Inc. is seeking a Quality Systems Engineer in Wilmington, MA to develop and maintain quality management systems for medical devices. Responsibilities include supporting compliance with ISO 13485 and FDA regulations, coordinating training activities, and...
$90k - $102k
Spectra Medical Devices, LLC in Wilmington, Massachusetts is seeking a Quality Engineer, Level II to ensure compliance with quality standards in medical device manufacturing. The ideal candidate will hold a Bachelor’s degree and have 2-4 years of experience in Quality Engineering...$100k - $110k
Sedaa Corporation is seeking a Mechanical Engineer in Burlington, MA, to lead the development of Mechanical Circulatory Support devices. The role requires expertise in solving complex problems and involves cross-functional collaboration in the design, analysis, and testing...- A leading medical device firm in the U.S. is seeking a Mechanical Engineer with over 6 years of experience in mechanical design and development. The ideal candidate will have a Bachelor's degree in Mechanical Engineering and demonstrate expertise in CAD design, specifically...
- ManpowerGroup Global, Inc. is seeking a Mechanical Engineer IV to support the Heart Failure R&D division. Located in Burlington, MA, this role involves designing innovative medical device components and collaborating with cross-functional teams to ensure product compliance...
$61.3k - $122.7k
Abbott Laboratories is seeking a Quality Engineer for our Westford, MA location in the Vascular division. This fully onsite role will involve providing Process and Quality Engineering support to manufacturing and product development, ensuring delivery of the highest quality...Work experience placement- ...in Burlington, MA is seeking a Mechanical Engineer IV to lead technical projects in developing Mechanical Circulatory Support devices. The chosen candidate will work on LVADs and... ...in CAD tools. Benefits include medical plans, 401(k), and various insurances. #J...
$115k - $182k
Philips Iberica SAU is seeking a Software Test Engineer in Bedford, MA, to join a high-performing team focused on verifying software solutions in the cardiovascular diagnostic space. You will collaborate closely with other teams, ensuring the software meets all functional...3 days per week- Anika is looking for a Senior Process Engineer to lead process improvement initiatives in medical device manufacturing. This role requires the design, validation, and implementation of equipment compliant with cGMP standards. Candidates must have a Bachelor’s degree in...
$102.48k - $163.97k
Mass Digital Health is looking for a Software Design Quality Engineer located in Bedford, MA. You will be responsible for developing and managing comprehensive software quality documentation, ensuring regulatory compliance throughout the software lifecycle. The ideal candidate...Full time- Philips International is seeking a Software Test Engineer for their Bedford, MA location. In this role, you will validate software solutions in the cardiovascular diagnostic space to ensure they meet functional, safety, and performance standards. We're looking for a candidate...Full timeWork at office
- Hiring for Senior Mechanical Engineer - R&D in Burlington, MA Seeking... ...Circulatory Support (MCS) devices, specifically Left Ventricular... ...development of implantable Class III medical devices Design, analyze,... ...cross‑functionally with R&D, Quality, Regulatory, Manufacturing,...
- BrioHealth Solutions, Inc. is looking for a Staff/Principal Mechanical Engineer in Burlington, Massachusetts, to lead the design and development of complex Class III implantable medical devices. This highly visible role demands extensive experience in regulated medical...
- LeMaitre is seeking an R&D Engineer in Burlington, Massachusetts, to develop and manufacture medical devices. The position involves working with a multi-disciplinary team, tackling responsibilities such as product testing, data analysis, and validation protocols. Ideal...
$160k - $190k
Werfenlife SA. seeks an experienced Engineering Manager in Bedford, Massachusetts, to lead technology management across projects in medical devices. The ideal candidate will have over 15 years of experience in engineering, proven leadership of teams, and expertise in risk...- Theuniversityunion is seeking a Principal Validation Engineer in Bedford, MA to lead validation strategies for medical device products and manufacturing processes. Ideal candidates will have over 10 years of experience, strong leadership skills, and expertise in compliance...
$90k - $120k
Werfenlife SA. is seeking an Engineer III to support systems engineering programs in a regulated medical device setting. This role emphasizes hands-on contributions to software-related investigations and complex problem troubleshooting, engaging collaboratively across...$90k - $120k
Werfen North America in Bedford, Massachusetts is looking for an Engineer III to support software systems in a regulated medical device environment. The ideal candidate should have extensive experience in software-driven systems and technical investigations. This position...$90k - $120k
Werfen is seeking an Engineer III to contribute to systems engineering programs in a regulated medical device environment. This role involves troubleshooting software and systems issues, leading investigations, and supporting cross-functional teams. Ideal candidates will...$135k - $160k
Access Vascular is seeking a Senior Designs Assurance Quality Engineer located in Billerica, Massachusetts. The role involves managing... ...control processes and providing quality engineering support for medical device product families. Candidates should have a BS in...$130k - $175k
LeMaitre Vascular in Burlington, MA is seeking a hands-on Engineer to lead testing protocol development for Class I, II, and III medical devices. The role includes managing product life cycle engineers and ensuring regulatory compliance with industry standards. Candidates...- ...experienced Principal Validation Engineer with 10+ years' experience to... ...strategy and execution for medical device products, manufacturing processes... ...impact. Collaborate with Quality, Manufacturing, R&D, Regulatory Affairs, and suppliers. Analyze validation data and...For contractorsVisa sponsorshipWork visaFlexible hours
$99k - $158k
Mass Digital Health is seeking an Instrument Control Software Engineer specializing in C++ for medical device software development in Bedford, MA. This role requires expertise in C++ and the Qt Framework to ensure accurate control of medical instruments. The candidate should...Full time$220k - $260k
...dedication to innovation and quality. We’re passionate about... ...Overview Job Summary The Director, Strategic Programs & Business... ...advanced degree in business, engineering, or life sciences preferred.... ...leadership roles within the medical device, healthcare, pharmaceutical,...Work experience placementWorldwide$122.4k - $183.6k
...millions of people worldwide. As a test engineer within the CST Enabling Technologies... ...tasks include: Evaluate requirements for quality and completeness to ensure they meet... ...Understanding of federal and international medical device regulations, such as FDA QSR, ISO 14971...H1bWork at officeLocal areaWorldwideFlexible hours
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