Enhanced Compliance Inc. Jobs Hiring Now
Enhanced Compliance Inc. is hiring for 20 open roles on Migrate Mate as of July 16, 2026, concentrated in engineering (Non-Software) and cloud & DevOps. Migrate Mate updates Enhanced Compliance Inc.'s live openings daily. Enhanced Compliance Inc. is a medical device consulting and quality engineering firm supporting product development, regulatory compliance, and validation across the medical device industry.
Find Enhanced Compliance Inc. JobsOverview
Enhanced Compliance Inc. hiring data on Migrate Mate, as of July 16, 2026.
- Open jobs
- 20
- Top team
- Engineering (Non-Software)
- Seniority
- Manager level or above
- Work type
- 0% remote or hybrid
- Top location
- Marlborough
Open Roles at Enhanced Compliance Inc.
Showing 20 of 20+ Enhanced Compliance Inc. jobs
About ECI
ECI’s mission is to be the global leader of professional consulting services for the life sciences industry. Our clients lean on our diverse perspectives and decades of expertise to tackle their toughest challenges, and we take pride in providing them transformative solutions with distinctive, sustainable and long-term value. ECI boasts a proven track record of providing full product life cycle consulting on a variety of challenging and exciting projects. Our collaborative culture, welcoming team and flexible employment & benefit options allow us to maintain strong relationships with the most talented individuals in the life sciences industry.
As a Design Quality Assurance Engineer, you will ensure that all requirements are met for the Product Lifecycle Process, Risk Management, Design Controls, and Usability Testing. You will work in fast-paced cross-functional teams to maintain and support quality-engineering methodologies, systems, and practices that meet company, customer, and regulatory requirements.
- Provide quality and compliance input to project teams for decisions and deliverables (e.g., Design Change Analysis, Design Inputs, Design Outputs, Test Methods, Design Review, Design V&V, Usability Testing, Process Validation, and Labeling)
- Support Risk Management planning, updating and maintenance of the product risk documentation in compliance with regulatory standards
- Support Usability Engineering and planning documentation
- Support the implementation of effective quality assurance, process controls, statistical analyses, and metrics
- Provide key quality trending information and data
- Offer quality and compliance input for post-market activities such as design changes, supplier auditing, and customer complaint investigations
- Identify, prioritize, communicate, and resolve quality issues
- Lead implementation activities for post-market surveillance, product feedback, and corrective and preventive action programs
- Support internal and external audits
- Bachelor’s Degree in Biomedical/ Mechanical/ electrical engineering or equivalent is required
- Minimum of 5 years direct experience in medical device industry preferred
- Ability to perform work accurately and thoroughly
- Ability to communicate effectively in written and oral form
- Excellent report writing skills essential along with the ability to find a solution or deal proactively with work related problems
- Ability to develop and sustain positive relationships with internal as well as external customers
- Good analytical and problem-solving skills
- Broad and in depth regulatory knowledge in medical device (Class II and III medical devices)
- Vast experience in writing/reviewing design control documents and compilation of DHFs
- Experience with Minitab Statistical software
ECI is an equal opportunity employer.
All qualified applicants will receive consideration for employment at ECI without regard to race; creed; color; religion; national origin; sex; age; disability; sexual orientation; gender identity or expression; genetic predisposition or carrier status; veteran, marital, or citizenship status; or any other status protected by law. At the time of this posting, all candidates must be authorized to work in the U.S. without the need for employment-based visa sponsorship now or in the future. At the time of this posting, ECI will not sponsor applicants for U.S. work visa status for this opportunity.
About ECI
ECI’s mission is to be the global leader of professional consulting services for the life sciences industry. Our clients lean on our diverse perspectives and decades of expertise to tackle their toughest challenges, and we take pride in providing them transformative solutions with distinctive, sustainable and long-term value. ECI boasts a proven track record of providing full product life cycle consulting on a variety of challenging and exciting projects. Our collaborative culture, welcoming team and flexible employment & benefit options allow us to maintain strong relationships with the most talented individuals in the life sciences industry.
As a Design Quality Assurance Engineer, you will ensure that all requirements are met for the Product Lifecycle Process, Risk Management, Design Controls, and Usability Testing. You will work in fast-paced cross-functional teams to maintain and support quality-engineering methodologies, systems, and practices that meet company, customer, and regulatory requirements.
- Provide quality and compliance input to project teams for decisions and deliverables (e.g., Design Change Analysis, Design Inputs, Design Outputs, Test Methods, Design Review, Design V&V, Usability Testing, Process Validation, and Labeling)
- Support Risk Management planning, updating and maintenance of the product risk documentation in compliance with regulatory standards
- Support Usability Engineering and planning documentation
- Support the implementation of effective quality assurance, process controls, statistical analyses, and metrics
- Provide key quality trending information and data
- Offer quality and compliance input for post-market activities such as design changes, supplier auditing, and customer complaint investigations
- Identify, prioritize, communicate, and resolve quality issues
- Lead implementation activities for post-market surveillance, product feedback, and corrective and preventive action programs
- Support internal and external audits
- Bachelor’s Degree in Biomedical/ Mechanical/ electrical engineering or equivalent is required
- Minimum of 5 years direct experience in medical device industry preferred
- Ability to perform work accurately and thoroughly
- Ability to communicate effectively in written and oral form
- Excellent report writing skills essential along with the ability to find a solution or deal proactively with work related problems
- Ability to develop and sustain positive relationships with internal as well as external customers
- Good analytical and problem-solving skills
- Broad and in depth regulatory knowledge in medical device (Class II and III medical devices)
- Vast experience in writing/reviewing design control documents and compilation of DHFs
- Experience with Minitab Statistical software
ECI is an equal opportunity employer.
All qualified applicants will receive consideration for employment at ECI without regard to race; creed; color; religion; national origin; sex; age; disability; sexual orientation; gender identity or expression; genetic predisposition or carrier status; veteran, marital, or citizenship status; or any other status protected by law. At the time of this posting, all candidates must be authorized to work in the U.S. without the need for employment-based visa sponsorship now or in the future. At the time of this posting, ECI will not sponsor applicants for U.S. work visa status for this opportunity.
Job Roles at Enhanced Compliance Inc.
Working at Enhanced Compliance Inc.
Enhanced Compliance Inc.'s 20 open roles are manager level or above, and about 0% are remote or hybrid. The most active teams are engineering (Non-Software), cloud & DevOps, and content marketing. Enhanced Compliance Inc. provides quality engineering, regulatory compliance, and product development support to medical device companies, with expertise spanning design quality assurance, process validation, software quality, and R&D engineering. The firm works across the medical device lifecycle, from early-stage development through manufacturing and regulatory submission. Most Enhanced Compliance Inc. roles are based in Marlborough, with some in Remote and Santa Clarita.
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Browse jobs by roleEnhanced Compliance Inc. Jobs: Frequently Asked Questions
How many jobs is Enhanced Compliance Inc. hiring for right now?
Enhanced Compliance Inc. is hiring for 20 open roles on Migrate Mate as of July 16, 2026, updated daily, concentrated in engineering (Non-Software) and cloud & DevOps. Roles span quality engineering, process validation, software quality assurance, and R&D, primarily within the medical device sector. Migrate Mate reflects Enhanced Compliance Inc.'s current openings as they are posted.
What kinds of roles does Enhanced Compliance Inc. hire for?
The most active teams are engineering (Non-Software), cloud & DevOps, and content marketing. Enhanced Compliance Inc. consistently hires for medical device quality engineering, design quality assurance, process and principal validation, software quality assurance, systems engineering, and R&D engineering positions. Most postings are manager level or above, reflecting the specialized technical expertise the company's work requires.
Are Enhanced Compliance Inc. jobs remote or in-person?
Mostly on-site. About 0% of Enhanced Compliance Inc.'s open roles on Migrate Mate are remote or hybrid as of July 16, 2026, with the rest based in Marlborough. Each Enhanced Compliance Inc. listing shows its work location so you can filter before applying.
How do I apply to a job at Enhanced Compliance Inc.?
Find a role that fits your background by browsing Enhanced Compliance Inc.'s open positions on Migrate Mate, then follow the listing through to Enhanced Compliance Inc.'s own application process. Enhanced Compliance Inc. manages its hiring directly, so all applications, interviews, and decisions are handled by their team.
Does Enhanced Compliance Inc. hire entry-level?
Most of Enhanced Compliance Inc.'s open roles on Migrate Mate are manager level or above as of July 16, 2026. Entry-level openings are limited. Check individual Enhanced Compliance Inc. listings for stated experience requirements.
Where is Enhanced Compliance Inc. hiring?
Most Enhanced Compliance Inc. roles are based in Marlborough, with some in Remote and Santa Clarita, and about 0% offer remote or hybrid work as of July 16, 2026. Migrate Mate shows the location on each listing.