- Working knowledge of Design Controls. Provide quality and compliance input to project teams for project decisions and deliverables (i.e. Design Change Analysis, Design Inputs, Design Outputs, Test Methods, Design Reviews, Design V&V, Usability Testing, SW Validation, Process Validation and Labeling).
- Creation and review of Risk Management documentation such as Hazard Analysis, Task Analysis, Design Failure Mode, and Effects Analysis (DFMEA) and Fault Tree Analysis (FTA). Understand and support linkage of field data and Risk Management
- Apply sound, systematic problem-solving methodologies in identifying, prioritizing, communicating, and resolving quality issues (i.e. 5 Whys analysis, Is-Is Not analysis, DMAIC problem solving methodologies).
- Provide quality guidance to assure country specific compliance.
- Champion compliance to company policies, work instructions and SOPs.
- Fully conversant with validation techniques and associated regulatory requirements including analysis of customer feedback and complaints.
- Support effective quality assurance, process controls and metrics using data and statistical analysis to drive improvements and actions for manufacturing and assembly of products.
- Provide quality and compliance input for post market product sustaining activities, such as design changes, supplier auditing and surveillance, design concessions, product CE marking and safety certification, customer complaint investigations, NCEP's, CAPA's PIRs, Field Signals Evaluations and Field Actions.
- Support internal and external regulatory audits as required.
- Support collection and analysis of key quality trending information and data for Management Review and Complaint Reviews.
- Bachelor's Degree in Mechanical, Electrical, Biomedical Engineering, or related degree.
- Minimum of 5 years of Medical Device engineering experience with a Bachelor's Degree OR a minimum of 3 years Medical Device engineering experience with a Master's Degree.
- Working knowledge of the FDA, ISO, EUMDR and the medical device industry quality requirements associated with product development, design controls, product risk management, and usability engineering.
- Travel approximately 10-25%
- Strong communication (oral and written) and presentation skills.
- Ability to collaborate and work on a global team.
- Previous Experience in integrations.
- Focus on detailed work with emphasis on accuracy and completeness.
- Excellent organizational and planning skills; drives for results.
- High energy problem solver capable of driving items to closure.
- Minitab Statistical Analysis software (or equivalent).
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Senior Design Quality Assurance Engineer - Marlborough, United States - Boston Scientific
Description
Additional Location(s): N/ADiversity - Innovation - Caring - Global Collaboration - Winning Spirit - High Performance
At Boston Scientific, we'll give you the opportunity to harness all that's within you by working in teams of diverse and high-performing employees, tackling some of the most important health industry challenges. With access to the latest tools, information and training, we'll help you in advancing your skills and career. Here, you'll be supported in progressing - whatever your ambitions.
About the Role: At Boston Scientific, the Design Assurance Engineer Integrations is a quality engineer that directly supports medical device product development and integration from an acquired system to BSCs Quality system, including design controls. This individual will work with high-performance cross-functional development team to ensure safety, quality and compliance of acquired products while continuously improving their commercial value. Initially, this position supports the transition of the acquired devices to meet regulations and BSC requirements. This position is part of the design site for the Endoscopy division and can support activities including but not limited to New Product Development, Sustaining and Life Cycle Management and Quality Systems initiatives as they relate to design and development.
Provides quality engineering support to operations, product development and sustaining projects for current products on the market. Develops, establishes, and maintains quality-engineering methodologies, systems, and practices which meet BSC, customer, and regulatory requirements. Serves as a Quality representative to improve awareness, visibility, and communication on quality initiatives to support assigned departmental, functional, site, divisional and corporate quality goals, and priorities. Provides quality engineering support within acquired products, technical development projects, new product development projects, sustaining existing product families, or system/services support.
This is a hybrid position based out of Marlborough, MA with the expectation to be in the office a minimum of two days per week.
Your Responsibilities Will Include:
Among other requirements, Boston Scientific maintains specific prohibited substance testing requirements for safety-sensitive positions. This role is deemed safety-sensitive and, as such, candidates will be subject to a drug test as a pre-employment requirement. The goal of the drug testing is to increase workplace safety in compliance with the applicable law.
As a leader in medical science for more than 40 years, we are committed to solving the challenges that matter most - united by a deep caring for human life. Our mission to advance science for life is about transforming lives through innovative medical solutions that improve patient lives, create value for our customers, and support our employees and the communities in which we operate. Now more than ever, we have a responsibility to apply those values to everything we do - as a global business and as a global corporate citizen.
So, choosing a career with Boston Scientific (NYSE: BSX) isn't just business, it's personal. And if you're a natural problem-solver with the imagination, determination, and spirit to make a meaningful difference to people worldwide, we encourage you to apply and look forward to connecting with you
At Boston Scientific, we recognize that nurturing a diverse and inclusive workplace helps us be more innovative and it is important in our work of advancing science for life and improving patient health. That is why we stand for inclusion, equality, and opportunity for all. By embracing the richness of our unique backgrounds and perspectives, we create a better, more rewarding place for our employees to work and reflect the patients, customers, and communities we serve. Boston Scientific is proud to be an equal opportunity and affirmative action employer.
Boston Scientific maintains a prohibited substance free workplace. Pursuant to Va. Code § , Boston Scientific is providing notification that the unlawful manufacture, sale, distribution, dispensation, possession, or use of a controlled substance or marijuana is prohibited in the workplace and that violations will result in disciplinary action up to and including termination.
Please be advised that certain US based positions, including without limitation field sales and service positions that call on hospitals and/or health care centers, require acceptable proof of COVID-19 vaccination status. Candidates will be notified during the interview and selection process if the role(s) for which they have applied require proof of vaccination as a condition of employment. Boston Scientific continues to evaluate its policies and protocols regarding the COVID-19 vaccine and will comply with all applicable state and federal law and healthcare credentialing requirements. As employees of the Company, you will be expected to meet the ongoing requirements for your roles, including any new requirements, should the Company's policies or protocols change with regard to COVID-19 vaccination.
