Senior R&D Engineer - Medical Device #1380

Enhanced Compliance Inc.; Marlborough (MA); On-site; USD 110,000 - 170,000; Full time

Benefits offered by this job

Equal opportunity employer

Flexible benefits

Job summary

Enhanced Compliance Inc. is seeking a seasoned Quality/Regulatory professional to drive compliance across medical devices from design through validation. The role focuses on quality input, documentation, and adherence to FDA/ISO standards.

You will collaborate with cross-functional teams to ensure robust design controls, risk management, and verification activities. Strong communication and team leadership are essential in this contractor/FT capacity.

Qualifications

• 5–6 years' direct R&D experience in medical devices (electromechanical).
• Experience with durable medical capital equipment preferred.
• Excellent written and verbal communication with good presentation skills.
• Knowledge of FDA Quality Systems Regulations (21 CFR 820) required.
• Demonstrated use of quality tools: SPC, DOE, GR&R, FMEA, CAPA, and process validation.
• Must understand FDA 21CFR820, ISO 13485, 14971, 11607 standards.

Responsibilities

• 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).
• Develop quality documentation such as quality plans and SOPs; ensure FDA/ISO compliance.
• Represent Quality initiatives during design and phase reviews; lead quality practices.
• Lead implementation of Acceptance Activities, First Article Inspections, sampling plans, and product testing.
• Apply systematic problem-solving to identify and resolve quality issues; support CAPA/NCRs/Complaints.
• Assist with special projects as needed.

Skills

Quality assurance

Regulatory compliance

SOP writing

DOE

CAPA

Statistical methods

Design review

FDA knowledge

Education

Bachelor's degree

Tools

SPC

FMEA

GR&R

DOE

Job description

• Location Marlborough, MA,Marlborough, MA, 01752,United States
• Employee Type Contractor or FT Employee
• Required Degree 4 Year Degree

Description

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.

What You'll Do

• 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).
• Develop quality documentation such as quality plans, standard operating procedures, and inspection procedures. Ensure regulatory, FDA, and ISO compliance in all areas of responsibilities.
• Represent Quality initiatives and compliance when participating and Design and Phase reviews
• Serve as an effective leader and team member in supporting quality disciplines, decisions, and practices.
• Ensure that required standards for products are documented in the product requirements (PR) specification and ensure compliance by performing quarterly gap analysis and reviewing applicable verification documentation.
• Ensure the use of statistically valid sampling techniques and teach others on the use of these and other advanced statistical techniques such as DOE and ANOVA evaluations.
• Provide direction and lead the implementation of Acceptance Activities, First Article Inspections, In-Process Inspections, Sampling Plans, product/component testing, inspections, and acceptance criteria.
• Apply sound, systematic problem-solving methodologies in identifying, prioritizing, communicating, and resolving quality issues.
• Provide support for CAPA/NCRs/Complaints
• Assists with special projects as needed.

What We Look For

• Minimum of 5-6 years’ direct R&D experience in medical device industry working with electromechanical devices
• Experience with durable medical capital equipment in addition to single-use devices is preferred
• Excellent written and verbal communication skills with good presentation and technical writing skills
• Collaborative attitude with the ability to work well in a team environment
• Strong engineering, design, and analysis skills along with experience with medical devices from concept to commercialization
• Understanding of FDA Quality Systems Regulations
• Demonstrated use of quality tools and methodologies including SPC, DOE, GR&R, FMEA, CAPA, and process validation (IQ, OQ/PQ).
• Must have a good understanding of FDA 21CFR820, ISO 13485, 14971, and 11607 standards.

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.