Manufacturing Engineer III
Boston Scientific · Quincy, MA
- Level
- Senior
- Team
- Manufacturing
- Degree
- Required
- Experience asked
- 4+ years
- Industry
- Medical devices
- Posted
- 30+ days ago
The role in 30 seconds
A senior manufacturing role at Boston Scientific (medical devices) in Quincy, MA. Develop, implement and optimize manufacturing processes to support product postponement, kitting, rework and related production activities.
- They ask for
- 4+ years · degree required
- Tools it names
- Lean, Root cause, Validation (IQ/OQ/PQ), Automation
- Day to day
- relocation help
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At a glance
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How to get in at this plant
Five moves over a week or two. The first one takes ten minutes.
- 1
Pick 2–3 people on the Manufacturing team at Boston Scientific
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- 2
Send a short, curious note
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- 3
Turn a reply into a short call
Questions worth asking about this team:
- What does a normal week look like on your team?
- Is the work mostly new product launches or sustaining existing lines?
- How much time do you spend on the floor versus at a desk?
- How did you land the job? What stood out in your interviews?
- 4
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- 5
Bring proof to the interview
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About the role
About the role
Boston Scientific was recognized by Forbes as one of the Best Workplaces for Engineers in 2026, reflecting a culture where engineers do meaningful work.
Boston Scientific was recognized as a Glassdoor Best Place to Work in 2026, ranking No. 15 on the Top 100 list, reflecting the culture our employees experience every day.
This role provides manufacturing engineering support to the Production department at the Boston Scientific site in Quincy, Massachusetts, which supports medical device kitting, rework and postponement activities. As a Manufacturing Engineer III, you will play a key role in advancing Boston Scientific's global Ideal Product Flow (IPF) initiative, with a focus on new product introduction, process development and operational excellence.
You will independently lead and execute engineering activities, partner with cross-functional teams and apply technical expertise to develop and improve manufacturing processes. This role provides an opportunity to influence site performance, lead value improvement initiatives and serve as a technical resource to engineers and production teams.
requirements
while ensuring successful execution.
- ✓Partner cross-functionally with Production, Quality, Operations, Supply Chain and other internal and external stakeholders to deliver project and business objectives.
- ✓Prepare technical reports, documentation and presentations to communicate project status, recommendations, risks and results to key stakeholders.
- ✓Develop deep technical knowledge of product postponement processes and serve as a technical resource for the site and broader organization.
- ✓Build and leverage internal and external networks to identify resources, share best practices and resolve complex technical challenges.
- ✓Support the training and development of engineers, technicians and production employees by sharing technical knowledge and best practices.
- ✓Evaluate emerging technologies and manufacturing capabilities to identify opportunities that support business and operational objectives.
qualifications
- ✓Bachelor's degree in engineering.
- ✓Minimum of 4 years' experience in an engineering role, with demonstrated experience in new product introduction, process development or product/process implementation.
- ✓Working knowledge of process verification and validation principles and practices.
- ✓Demonstrated experience leading engineering projects and working effectively with cross-functional teams.
- ✓Demonstrated ability to analyze technical problems, develop solutions and drive improvements in a manufacturing environment.
Preferred qualifications
- ✓Experience in medical device or other regulated manufacturing environments.
- ✓Experience with packaging and labeling processes.
- ✓Experience with manufacturing automation equipment.
- ✓Experience with Lean manufacturing, continuous improvement or value improvement methodologies.
- ✓Experience supporting new product introduction or manufacturing transfer initiatives.
Minimum Salary: $ 82100
Maximum Salary: $ 156000
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Additional Location(s): N/A
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.
Work model, sponsorship, relocation
This role requires an on-site work model at our Quincy, Massachusetts, location, with employees expected to be on-site five days per week. Boston Scientific will not offer sponsorship or take over sponsorship of an employment visa for this position at this time. Relocation assistance is not available for this position at this time.
Your
will include
- •Lead and execute technical activities supporting new product and process introductions aligned with strategic business objectives, including the global IPF initiative.
- •Develop, implement and optimize manufacturing processes to support product postponement, kitting, rework and related production activities.
- •Lead process verification and validation activities, including development of protocols, execution, data analysis and documentation.
- •Identify and lead value improvement initiatives that enhance quality, cost, capacity, efficiency and operational performance.
- •Analyze manufacturing processes and use engineering principles and data-driven problem-solving methodologies to identify root causes and implement sustainable solutions.
- •Drive improvements in process design, manufacturing layout, workflow and operational performance.
- •Lead engineering projects of moderate complexity, establishing project objectives, deliverables, timelines and resource