Senior Quality Engineer - Medical Device Engineer #5452

Theuniversityunion; Taunton (MA); On-site; USD 90,000 - 140,000; Full time

Job summary

ECI seeks a Senior Quality Engineer to enhance production processes with cross-functional collaboration, ensuring efficiency, quality, and safety. You will support QS integration, maintain compliance matrices, and contribute to Design Assurance activities including DV, DVAL and Usability.

You will review change requests, develop quality docs, and lead quality initiatives across product and process reviews in a regulated medical-device environment.

Qualifications

• Minimum five (8) years direct Quality/Design Quality engineering experience in medical device industry.
• Must demonstrate use of quality tools/methodologies including SPC, DOE, GR&R, FMEA, CAPA, and process validation.
• Understanding of FDA 21 CFR 820, ISO 13485, 14971, and 11607 standards.
• Excellent written and verbal communication skills; strong presentation and technical writing skills.

Responsibilities

• Review and approve change requests related to Product, Process, and Validation and Verification documentation.
• Develop quality documentation such as quality plans, SOPs, and inspection procedures; ensure FDA/ISO compliance.
• Represent Quality initiatives during Design and Phase reviews.
• Identify industry best practices and lead quality disciplines and decisions.
• Ensure product requirements are documented in PR specs and verify via quarterly gap analyses.
• Apply statistically valid sampling techniques and teach others DOE/ANOVA and related methods.
• Review and approve PQs, TVs, GR&R, DOE, FMEA, CAPA, and master plans.
• Provide support for CAPA/NCRs/Complaint evaluations.
• Lead Acceptance Activities, First Article Inspections, In-Process Inspections, Sampling Plans, product testing and acceptance criteria.
• Apply systematic problem-solving to quality issues.
• Assist in special projects as needed.
• Contribute to team effort by performing related duties.

Skills

Quality engineering

DOE

GR&R

FMEA

CAPA

Process validation

FDA 21 CFR 820

ISO 13485

Education

Bachelor's degree in Engineering or related field

Tools

Microsoft Office

Job description

• Job Category ECI
• 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.

About the role

The Senior Quality Engineer primary role is to enhance production processes to ensure efficiency, quality, and safety. This role requires collaboration with cross-functional teams, strong problem-solving abilities, and a deep understanding of manufacturing systems to drive success. The roles will support Quality System integration deliverables including but not limited to maintaining site compliance matrix, updating acquired entity’s QS as the QS is integrated, maintain and update quality plans associated with integration activities. In addition, support and execute Design Assurance deliverables for product integration activities including DV, DVAL and Usability.

What you\'ll do

• Review and approve change requests related to Product, Process, and Validation and Verification documentation.
• 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
• Identify industry best practices. Act as an effective leader or 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
• Review and approve Process Qualifications, Test Method Validations, Gage R&R\'s, Process Capability studies, Design of Experiment (DOE), FMEAs (Design and Process), and production master control plans.
• Provide support for CAPA/NCRs/Complaint 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.
• Assists in special projects as needed.
• Contributes to team effort by accomplishing related duties as requested.

What you will bring

• Minimum of five (8) years direct Quality/Design Quality engineering experience in medical device industry required.
• Demonstrated used of quality tools/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.
• Demonstrated interpersonal skills with the ability to work within a team environment.
• Excellent written and verbal communication skills with good presentation and technical writing skills. Proficiency in all Microsoft Office programs.
• Good analytical and problem-solving skills. Strong engineering, design, and analysis skills.
• Working knowledge of tooling and manufacturing processes.
• Experience with medical devices from concept to commercialization.
• Understanding of FDA Quality Systems Regulations.

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.