New Product Introduction Quality Engineer

Akkodis; Jacksonville (FL); On-site; USD 55,104 - 61,992; Full time

Benefits offered by this job

Medical insurance

Dental insurance

Vision insurance

401K plan

Paid Sick Leave

Short-term disability

Job summary

A leading technology solutions company is seeking a Quality Engineer for a 6-month contract role in Jacksonville, Florida. This position involves quality governance activities, including participation in Technical Review Boards and supporting Change Control processes in a regulated medical device environment. The ideal candidate has experience in quality engineering within the medical sector and strong skills in compliance and documentation. Benefits include medical, dental, vision, and a flexible 401K plan.

Qualifications

• Experience working as a Quality Engineer in medical device or regulated industry.
• Hands-on exposure to TRB or similar technical review forums.
• Strong experience with Change Control / ECO / CR / CCB processes.

Responsibilities

• Participate in Technical Review Board discussions and provide risk-based quality input.
• Support Change Control Board activities including impact assessment.
• Review engineering changes for compliance and quality impact.

Skills

Quality Engineering in medical devices

Change Control processes

Documentation skills

Cross-functional collaboration

Risk Management

Job description

Akkodis is seeking a Quality Engineer for a 6-month contract role in Jacksonville, FL. This role focuses on quality governance activities including Technical Review Board (TRB) participation, Change Control Board (CCB) support, and ensuring compliance within a regulated medical device environment.

To be considered, candidates must have experience working within structured change control processes, cross-functional quality reviews, and regulated quality systems.

Pay Range: $40/hr. –45/hr. on W2 (The pay rate may be negotiable based on experience, education, geographic location, and other factors.)

Quality Engineer responsibilities include:

• Participate in Technical Review Board (TRB) discussions and provide risk-based quality input
• Support Change Control Board (CCB) activities including impact assessment and documentation review
• Review engineering changes, deviations, and CAPA activities for compliance and quality impact
• Collaborate with R&D, Manufacturing, Supply Chain, and Quality teams
• Ensure alignment with FDA, ISO 13485, and GMP requirements
• Support validation strategy reviews and quality documentation updates
• Drive continuous improvement initiatives within regulated processes
• Maintain clear documentation and support audit readiness

Required Skills & Experience:

• Experience working as a Quality Engineer in medical device or regulated industry
• Hands-on exposure to TRB or similar technical review forums
• Strong experience with Change Control / ECO / CR / CCB processes
• Understanding of Design Controls, Risk Management, and CAPA
• Experience supporting validation or NPI activities
• Strong documentation and cross-functional collaboration skills

Nice-to-Have Skills:

• R&D or Design Quality exposure
• FDA-regulated manufacturing experience
• Agile or cross-functional program support

If you are interested in this role, then please click APPLY NOW. For other opportunities available at Akkodis, or any questions, feel free to contact me at [e-mail]

Equal Opportunity Employer/Veterans/Disabled

Benefit offerings available for our associates include medical, dental, vision, life insurance, short-term disability, additional voluntary benefits, an EAP program, commuter benefits, and a 401K plan. Our benefit offerings provide employees the flexibility to choose the type of coverage that meets their individual needs. In addition, our associates may be eligible for paid leave including Paid Sick Leave or any other paid leave required by Federal, State, or local law, as well as Holiday pay where applicable. Disclaimer: These benefit offerings do not apply to client-recruited jobs and jobs that are direct hires to a client.

To read our Candidate Privacy Information Statement, which explains how we will use your information, please visit https://www.akkodis.com/en/privacy-policy.

The Company will consider qualified applicants with arrest and conviction records in accordance with federal, state, and local laws and/or security clearance requirements, including, as applicable:

· The California Fair Chance Act

· Los Angeles City Fair Chance Ordinance

· Los Angeles County Fair Chance Ordinance for Employers