Design Quality Engineer (Andover, MA) at Smith Nephew

Andover, Massachusetts, United States -

Full Time

Start Date

Immediate

Expiry Date

11 Jul, 26

Salary

122500.0

Posted On

12 Apr, 26

Experience

2 year(s) or above

Remote Job

Yes

Telecommute

Yes

Sponsor Visa

Skills

Design Quality Engineering, Risk Management, ISO 13485, ISO 14971, Design Control, Medical Device Regulations, FDA Quality System Regulation, GMP, Verification and Validation, Statistical Analysis, Quality Assurance, SOP Development, Risk Analysis, Technical Documentation, Compliance, Medical Device Software

Industry

Medical Equipment Manufacturing

Description

Design Quality Engineer (Andover, MA) Life Unlimited. At Smith+Nephew we design and manufacture technology that takes the limits off living. To maintain the design integrity of Smith & Nephew Medical Ltd. (SNM) wound medical devices. Responsible for ensuring that the safety, performance and quality of new and existing products for SNM conform to established standards and are in compliance with all applicable global Quality System Regulations. What will you be doing? Role holder shall abide at all times to company policies & procedures, and the governing standards & regulations, including (but not limited to): Any Local Hull site or S+N Global Quality System / Health, Safety & Environment Policy, Procedure or Work Instruction contained in the individual’s training plans. Applicable standards as defined in the Quality Manual (including but not limited to): ISO 9001 - ISO 14001 - ISO 13485. Applicable regulations as defined in the Quality Manual (including but not limited to): EU Medical Device Directive / Regulation, Regulations issued by the 5 MDSAP Jurisdictions, UK Human Medicines & Medical Device Regulations, cGMP, cGDP (including 2013/C 343/01), cGLP as applicable for each role. To carry out day-to-day Design Quality activities for all marketed and NPD Advanced Wound Management products. This includes, but is not limited to: Ensuring compliance of design control and design change activities through the review and acceptance of design activities independently of the New Product Development (NPD) design team and/or sustaining engineering teams. Ensuring that Design History Files and other associated quality documentation are complete and compliant by means of review and approval. Work with NPD and/or sustaining engineering teams to ensure verification and validation outputs meet design inputs through the creation-review-execution of test cases and participation in product risk analyses and change reviews. Provide support to Operations and Quality Assurance (QA) teams to ensure successful transfer of the design to manufacturing, in accordance with all applicable regulations. Assist in the adoption of test methods, equipment acquisition for product testing, validations/qualifications, statistical analysis of data for significance and other requirements through review and approval of protocols and reports. Participate in the creation and approval of complete, unambiguous, and measurable design inputs. Review and approve specifications, including those for raw materials, intermediate products and finished products. To carry out day-to-day Risk Management activities for all marketed and NPD Advanced Wound Management products. This includes, but is not limited to: Generating and maintaining elements of the Risk Management File in line with design control and change control requirements. Contributing to Health Hazard Evaluation / Notification to Management processes where required for specific risk matters. To ensure satisfactory and timely completion of all risk control activities. To assist, where appropriate, in the preparation and analysis of information for Safety and Efficacy Review Board, including the identification of potential medical risks. To ensure that user instructions are complete and accurately reflect the product risk through contribution to, and approval of, IFU text. To provide guidance and support to the Advanced Wound Management Division in all areas of product risk management. To establish and sustain compliant and fit for purpose processes and procedures for the development and maintenance of safe, efficacious and high-quality medical devices and associated products. Ensure timely review of current SOPs and WoW. Continuously improve current SOPs and WoW to meet the ongoing needs of the business. To maintain the currency of knowledge required to carry out activities and responsibilities effectively through proactive personal development planning. What will you need to be successful? Bachelor's Degree in a relevant life science / engineering discipline with 2+ years of appropriate experience. Exposure of the requirements for and application of Risk Management for medical devices in accordance with ISO 14971. Exposure of the requirements for and application of Design Control for medical devices in accordance with ISO 13485. Exposure of relevant GMP and Quality Systems standards and specifically with FDA Quality System Regulation and ISO 13485. Experience of working in a regulated environment Experience with medical device software development in accordance with ISO 62304 is preferred. You Unlimited. We believe in creating the greatest good for society. Our strongest investments are in our people and the patients we serve. Inclusion and Belonging- Committed to Welcoming, Celebrating and Thriving on Inclusion and Belonging, Learn more about Employee Inclusion Groups on our website ( https://www.smith-nephew.com/). Your Future: 401k Matching Program, 401k Plus Program, Discounted Stock Options, Tuition Reimbursement Work/Life Balance: Flexible Personal/Vacation Time Off, Paid Holidays, Flex Holidays, Paid Community Service Day Your Wellbeing: Medical, Dental, Vision, Health Savings Account (Employer Contribution of $500+ annually), Employee Assistance Program, Parental Leave, Fertility and Adoption Assistance Program Flexibility: Hybrid Work Model (For most professional roles) Training: Hands-On, Team-Customized, Mentorship Extra Perks: Discounts on fitness clubs, travel and more! #LI-HYBRID "The anticipated base compensation range for this position is $81,750 - $122,500 USD annually. The actual base pay offered to the successful candidate will be based on multiple factors, including but not limited to job-related knowledge/skills, experience, geographical location, and internal equity. It is not typical for an individual to be hired at the high end of the range for their role at Smith + Nephew. Compensation decisions are dependent upon the facts and circumstances of each position and candidate. In addition to base pay, we provide competitive bonus and benefits, which include medical, dental, and vision coverage, 401k, tuition reimbursement, medical leave programs, and a variety of wellness offerings. " Smith+Nephew provides equal employment opportunities to applicants and employees without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, protected veteran status, or disability. Stay connected by joining our Talent Community. We're more than just a company - we're a community! Follow us on LinkedIn to see how we support and empower our employees and patients every day. Check us out on Glassdoor for a glimpse behind the scenes and a sneak peek into You. Unlimited., life, culture, and benefits at S+N. Explore our website and learn more about our mission, our team, and the opportunities we offer. Smith+Nephew is a global medical technology company. We design and manufacture technology that takes the limits off living. We support healthcare professionals to return their patients to health and mobility, helping them to perform at their fullest potential. From our first employee and founder, T.J. Smith, to our team today, it’s our people who make Smith+Nephew a unique place. Yes, we love to innovate and develop exciting technologies, and we offer competitive salaries and progressive benefits. But it’s our culture - of Care, Collaboration and Courage - that really sets us apart. Through a spirit of ownership and can-do attitude we work together to win. We’re a company of people who care about each other, about our customers and their patients, and about our communities. Together, we fulfill our shared purpose of Life Unlimited.

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Responsibilities

The Design Quality Engineer ensures the safety, performance, and quality of wound medical devices by maintaining design integrity and compliance with global regulations. They oversee design control activities, manage risk management files, and support the transfer of designs to manufacturing.