Job Title: Quality Engineer III

Job Description

We are seeking a highly experienced Quality Engineer to lead post-acquisition quality remediation efforts at our Irvine, CA site. This onsite role will focus on the remediation, standardization, and sustainment of Process Failure Mode and Effects Analyses (PFMEAs) and Test Method Validation (TMV) documentation to ensure compliance with internal quality standards and applicable regulatory requirements. This role is ideal for a seasoned medical device quality professional with strong expertise in risk management, test method validation, and measurement system analysis, capable of independently assessing legacy documentation, developing remediation strategies, and collaborating cross-functionally to integrate acquired products and processes into an established Quality Management System (QMS).

Responsibilities

Lead and execute PFMEA remediation activities, including gap assessments, risk re-evaluations, updates, and alignment to current manufacturing and process states.Own the remediation, development, and documentation of Test Method Validations (TMVs) for inspection, test, and measurement methods used in manufacturing and product verification.Evaluate legacy test methods for adequacy, robustness, and regulatory compliance; identify gaps and define remediation plans.Plan, execute, and review Gage Repeatability & Reproducibility (Gage R&R) studies as part of TMV and measurement system validation activities.Apply statistical techniques (e.g., GR&R, bias, linearity, stability) to assess measurement system capability and suitability.Ensure PFMEAs and TMVs comply with ISO standards, FDA Quality System Regulation (21 CFR 820), and internal quality procedures.Collaborate cross-functionally with R&D, Manufacturing Engineering, Quality Control, and Operations to define test requirements, acceptance criteria, and validation strategies.Support integration of acquired products, processes, and test methods into the parent company’s QMS.Review and approve TMV protocols, reports, and supporting statistical analyses.Facilitate risk management and PFMEA reviews to ensure test methods adequately detect and control product and process risks.Ensure TMV and PFMEA changes are properly documented and implemented through formal change control processes.Support internal and external audits, inspections, and diligence activities related to test method validation and measurement systems.Identify opportunities to improve test method robustness and long-term sustainment of validation practices.

Essential Skills

Bachelor’s degree in Engineering (Biomedical, Mechanical, Manufacturing, Industrial, or related field).5+ years of relevant Quality Engineering experience in the medical device industry.Proven experience leading PFMEA development and remediation.Strong hands-on experience with Test Method Validation (TMV).Familiarity and working knowledge of Gage R&R and measurement system analysis.Ability to interpret and apply statistical data to validate inspection and test methods.Solid working knowledge of ISO standards and FDA QSR (21 CFR 820).Experience supporting remediation efforts in a post-acquisition or compliance-driven environment.Ability to work onsite in Irvine, CA.Excellent technical writing, analytical, and documentation skills.Ability to work independently and effectively lead cross-functional teams.

Additional Skills & Qualifications

Experience validating mechanical, dimensional, functional, or analytical test methods.Proficiency with statistical software or analysis tools (e.g., Minitab, JMP, Excel).Experience supporting FDA inspections and/or notified body audits.Understanding of verification and validation (V&V) activities and their linkage to risk management.Experience with electronic QMS systems (e.g., Agile, Windchill, Arena, MasterControl).Medical device manufacturing, inspection, or metrology.

Work Environment

This role requires working onsite in Irvine, CA, within a dynamic and collaborative environment. Employees enjoy benefits such as 3 weeks of PTO and 10 paid holidays. The position involves a high level of interaction with cross-functional teams and the use of statistical software and electronic QMS systems.

Job Type & Location

This is a Contract position based out of Irvine, CA.

Pay and Benefits

The pay range for this position is $55.00 - $65.00/hr.

Eligibility requirements apply to some benefits and may depend on your job classification and length of employment. Benefits are subject to change and may be subject to specific elections, plan, or program terms. If eligible, the benefits available for this temporary role may include the following: • Medical, dental & vision • Critical Illness, Accident, and Hospital • 401(k) Retirement Plan – Pre-tax and Roth post-tax contributions available • Life Insurance (Voluntary Life & AD&D for the employee and dependents) • Short and long-term disability • Health Spending Account (HSA) • Transportation benefits • Employee Assistance Program • Time Off/Leave (PTO, Vacation or Sick Leave)

Workplace Type

This is a fully onsite position in Irvine,CA.

Application Deadline

This position is anticipated to close on Feb 19, 2026.

About Actalent

Actalent is a global leader in engineering and sciences services and talent solutions. We help visionary companies advance their engineering and science initiatives through access to specialized experts who drive scale, innovation and speed to market. With a network of almost 30,000 consultants and more than 4,500 clients across the U.S., Canada, Asia and Europe, Actalent serves many of the Fortune 500.

The company is an equal opportunity employer and will consider all applications without regard to race, sex, age, color, religion, national origin, veteran status, disability, sexual orientation, gender identity, genetic information or any characteristic protected by law.

If you would like to request a reasonable accommodation, such as the modification or adjustment of the job application process or interviewing due to a disability, please email actalentaccommodation@actalentservices.com for other accommodation options.