Job Title: Quality EngineerJob Description

This role provides lead quality support for new product development teams to ensure new and improved medical device products and processes comply with applicable standards and regulations. The Quality Engineer owns design quality activities to ensure adherence to design control systems, supports Design History File (DHF) creation, and helps drive timely regulatory approvals. The position plans and leads quality projects by organizing activities into realistic timelines and works collaboratively with cross-functional teams to build a strong,team-oriented environment.

Responsibilities

Provide lead quality support for new product development projects to ensure medical device products and processes comply with applicable standards and regulations.
Own design quality activities to ensure compliancewith design control systems for new and improved products.
Assist with all elements of the design control system and Design History File (DHF) creation for new product development from a design quality perspective.
Help execute within a quality assurance system that aligns with the established Quality Management System (QMS) while optimizing time to regulatory approval and clearance.
Collaborate with suppliers to review and drive engineering drawing reviews, gage development, capability studies, gage R&R studies, special process validations, tolerance stack-ups, CMM correlation studies, PFMEA, process flows, control plans, inspection plans, and Device History Record (DHR) reviews to ensure regulatory clearance and production readiness.
Develop and implement corrective and preventive action plans, including internal CAPAs and supplier SCARs, to address product and process issues.
Provide verification and validation, sampling, and statistical analysis support for all functions required for product clearance and approval, including supplier-related activities such as mechanical testing, manufacturing special processes, packaging, and sterilization.
Design and implement inspection methods, equipment, acceptance criteria, and sampling plans to support and qualify vendors.
Apply problem-solving methodologies, such as DMAIC, Shainin, and Ishikawa techniques, to identify root causes and implement effective solutions.
Use statistical tools and software to analyze process data, monitor process control, and assess process capability.
Interpret engineering drawings, including geometric dimensioning and tolerancing (GD&T), to define appropriate inspection methods and understand limitations based on tolerances.
Work effectively and productively with all departments, fostering a strong team atmosphere and building relationships within the organization and with external partners such as suppliers and regulatory agencies.
Communicate clearly in both oral and written form with multiple levels of the organization to report quality status, risks, and project progress.

Essential Skills

Proven experience as a Quality Engineer in the medical device industry, with strong involvement in new product development.
Strong experience with Risk Management documentation, including the creation, maintenance, and application of risk files for medical devices.
Demonstrated experience authoring and designing Design History Files (DHFs), including ownership of DHF structure, content, and compliance.
Hands-on experience working within design control systems for medical devices.
Bachelor's degree in an Engineering discipline.
Knowledge of design control requirements and applicable medical device regulations, including 21 CFR Part 820.
Working knowledge of quality system regulations and requirements, including 21 CFR Part 820 and ISO-based quality management standards.
Experience with corrective and preventive action (CAPA) processes and supplier corrective action requests (SCARs).
Ability to perform verification and validation activities, including sampling strategies and statistical analysis.
Proficiency in statistics, process control, and process capability analysis.
Ability to design and implement inspection methods, equipment, acceptance criteria, and sampling plans.
Strong communication skills, both oral and written, with the ability to interact effectively at multiple organizational levels.
Demonstrated ability to work collaboratively in a team environment and build productive relationships with cross-functional partners and external suppliers.

Additional Skills & Qualifications

Approximately 3 years of experience in quality engineering or a closely related role in the medical device industry is preferred.
Orthopedic medical device experience is highly preferred.
Experience with Hazard Analysis documentation is a strong plus.
Familiarity with ISO 9001 and other relevant quality management system standards.
Experience with problem-solving methodologies such as DMAIC, the Shainin System, and Ishikawa diagrams.
Experience applying statistics and statistical software (for example, Minitab) for data analysis and decision-making.
Experience using Computer-Aided Drafting (CAD) software such as NX or SolidWorks to review and interpret engineering designs.
Strong understanding of Geometric Dimensioning and Tolerancing (GD&T) and its impact on inspection and process capability.
Experience designing inspection methods and understanding inspection limitations based on engineering drawings and associated tolerances.
Ability to collaborate effectively with suppliers and regulatory agencies to support product approvals and ongoing compliance.
Strong organizational skills with the ability to plan and lead projects, sequence tasks, and manage realistic timelines.

Work Environment

The role is primarily onsite in Warsaw, with an expectation of working in the office four days per week for candidates within commuting distance. Remote candidates may be considered if they can be onsite in Warsaw for the first week of the role and travel to the site as project needs require, approximately 20% of the time. The work environment is collaborative and cross-functional, involving close interaction with engineering, quality, manufacturing, and supplier teams, as well as engagement with regulatory agencies. The position involves regular use of statistical analysis tools, CAD software, and quality management systems in a structured, regulated medical device setting.

Job Type & Location

This is a Contract position based out of Warsaw, IN.

Pay and Benefits

The pay range for this position is $40.00 - $53.00/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 remote position.

Application Deadline

This position is anticipated to close on Aug 14, 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 20,000 consultants and 5,000 clients across the U.S., Canada, Asia and Europe, Actalent serves many of the Fortune 500. We are proud to be an Engineering News-Record (ENR) Top 500 Design Firm for our engineering design services and a ClearlyRated Best of Staffing® winner for both client and talent service.

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 process due to a disability, please email actalentaccommodation@actalentservices.com for other accommodation options.

San Francisco Fair Chance Ordinance: Pursuant to the San Francisco Fair Chance Ordinance, for all positions located in the city and county of San Francisco, we will consider for employment qualified applicants with arrest and conviction records.

Massachusetts Lie Detector: It is unlawful in Massachusetts to require or administer a lie detector test as a condition of employment or continued employment. An employer who violates this law shall be subject to criminal penalties and civil liability.

Use of Artificial Intelligence (AI): We may use Artificial Intelligence (AI) to support parts of our hiring process, including sourcing, screening, and evaluating candidates. AI helps assess applications and qualifications, but final decisions are made by our hiring team. By applying, you acknowledge and agree that your application may be reviewed using AI tools.

Actalent

Latest Jobs

Remote Quality Engineer (42)

Remote Quality Engineer (34)