Senior Supplier Quality Engineer

We are seeking a Supplier Quality Engineer to support new product development initiatives, focusing on supplier quality and process readiness for product launches and regional expansions. The role involves translating product designs into manufacturing-ready processes, identifying and mitigating risks, and ensuring suppliers meet quality and compliance standards throughout the product lifecycle. You will work cross-functionally with engineering, supply chain, and manufacturing teams while playing a key role in process validation.

Responsibilities

• Translate design outputs and product specifications into production-ready controls and processes for supplier execution.
• Perform risk assessments, likely FMEA-based, and implement mitigation strategies across supplier and manufacturing processes.
• Lead or support validation efforts to ensure processes are stable, repeatable, and compliant with regulatory standards.
• Qualify, audit, and monitor suppliers to ensure compliance with GMP and Medtronic standards.
• Work alongside design, engineering, and supply chain teams to support product launches and design changes.
• Improve supplier capability, stability, and performance for long-term production success.

• 5 years of experience in Supplier Quality, Manufacturing Quality, or NPD Quality Engineering.
• Hands-on experience with process validation (IQ/OQ/PQ).
• Strong background in risk management, including FMEA and hazard analysis.
• Experience translating design outputs into manufacturing/production controls.
• Experience working in a regulated environment, preferably in medical devices, FDA/GMP.
• Bachelor’s degree in Engineering or a related field.

• Experience supporting new product development (NPD) or product launch activities.
• Experience with supplier audits and supplier qualification programs.
• Knowledge of large OEM systems.
• Experience with regional expansions or design changes in regulated environments.
• Familiarity with product line support, StealthAxis experience is a bonus.

This position is fully onsite in Lafayette, CO, with a standard 40-hour work week. You will work in a regulated, GMP-controlled environment, collaborating with engineering, supply chain, and manufacturing teams. The role is likely documentation-heavy, focusing on compliance, validation, and audit support.

Job Type & Location

This is a Contract position based out of Lafayette, CO.

The pay range for this position is $50.00 - $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)

This is a fully onsite position in Lafayette,CO.

This position is anticipated to close on Jul 22, 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.

Salary : $50 - $65