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Senior Quality Assurance Engineer

Work mode:  Hybrid
Onsite Location(s): 

Marlborough, MA, US, 01752

Additional Location(s): US-MA-Marlborough; US-CA-Valencia; US-IN-Spencer; US-MN-Arden Hills; US-MN-Maple Grove

Diversity - 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:
This role provides support to the Global Post Market team by leading integrations of companies acquired by Boston Scientific into Boston Scientific’s Post Market system(s) and processes, as well as supporting various projects resulting from regulation changes, business requirements or CAPAs. This role requires strong project management skills, quality system documentation skills, and a proficient understanding of Post Market processes and requirements. Responsibilities may include leading Post Market project teams, identifying key project deliverables, setting appropriate timelines aligning with project milestones, working with cross-divisional/functional representatives to gather required information, communicating project status to senior leadership, and supporting Post Market process improvements and initiatives.
 
Your Responsibilities Will Include:

  • Providing project management, including management of project teams and supporting quality system documentation, for Post Market projects
  • Coordinating parallel tasks and meetings to drive collaboration of multi-site and multi-functional stakeholders to support project deliverables and timelines
  • Leading Post Market workstream for acquisition integration projects
  • Ensuring compliance to US & OUS regulatory requirements
  • Collaborating with Post Market sites and teams
  • Providing audit support (backroom and storyboard preparation)
  • Collaborating with local and international Regulatory and Quality as required
  • Supporting and implementing new SOPs, WIs, and/or KSDs to improve and/or standardize Post Market processes
  • Supporting updates to impacted SOPs/WI
  • Identifying and ensuring training needs are addressed for Post Market requirements
  • Effectively identifying and escalating risks and working to resolve issues
  • Working independently across the organization
  • Participating in the Global Post Market Community
  • In all actions, demonstrating a primary commitment to patient safety and product quality by maintaining compliance to the Quality Policy and all other documented quality processes and procedures.
  • Traveling to support projects, as required 

 
What We're Looking For In You:
Required Qualifications

  • Bachelor’s degree, preferably in a scientific or technical discipline.
  • Minimum of 4+ years of medical device industry experience
  • Comprehensive understanding and working knowledge of Trackwise and/or SAS applications
  • Effective research and analytical skills.
  • Competency of Microsoft Office Suite (i.e., Word, Xcel, PowerPoint, Visio, etc.), and Statistical Analysis tools (or equivalent).
  • Working knowledge of FDA, ISO, MDD and the medical device industry quality
  • Strong research, communication, and presentation skills
  • Effective written and oral communication, technical writing, and editing skills
  • Travel approximately <5% of the time

 
Preferred Qualifications

  • Detailed understanding and working knowledge of US and International regulations including 21 CFR, 820, 210, 211, and 11 is required, as well as the Medical Device Directive, EN ISO 13485, EN ISO 14971, IEC 60601, and EN 62366.
  • Project Management Skills and Ability to manage multiple small projects.
  • CAPA experience.
  • Ability to work independently with minimal supervision
  • Agile/Scrum experience
     

Requisition ID: 590889

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 Corporation has been and will continue to be an equal opportunity employer. To ensure full implementation of its equal employment policy, the Company will continue to take steps to assure that recruitment, hiring, assignment, promotion, compensation, and all other personnel decisions are made and administered without regard to race, religion, color, national origin, citizenship, sex, sexual orientation, gender identify, gender expression, veteran’s status, age, mental or physical disability, genetic information or any other protected class.

 

Boston Scientific maintains a prohibited substance free workplace. Pursuant to Va. Code § 2.2-4312 (2000), 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.


Nearest Major Market: Boston

Job Segment: QA Engineer, Quality Engineer, Medical Device Engineer, QA, Quality Assurance, Engineering, Technology, Quality

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