Contract Medical Device Quality Engineer — Validation Lead

Inc. (Vti); Pendleton (SC); On-site; USD 55,000 - 96,000; Full time

Benefits offered by this job

4‑month contract

Project location Pendleton, SC

Job summary

VTI Life Sciences (VTI) seeks a forward-thinking Medical Device Quality Engineer for a 4‑month contract in Pendleton, SC. The role focuses on leading validation execution activities with operations and engineering teams for special processes, including laser marking and laser welding.

The candidate will review IQ/OQ/PQ protocols, execute validation activities on manufacturing equipment, and contribute to SOP development.

Qualifications

• Bachelor’s degree in Life Sciences, Computer Science, Engineering or related discipline.
• 2+ years of GMP-regulated Medical Device industry experience.
• Hands-on experience writing and executing validation protocols.
• Strong technical writing and documentation skills.
• Excellent organizational and project coordination abilities.

Responsibilities

• Lead and coordinate validation execution activities with operations and engineering teams for special process areas (Laser marking, Laser welding).
• Review IQ/OQ/PQ validation protocols and reports for equipment used for medical devices.
• Execute validation protocols for manufacturing equipment such as laser marking, laser welding, grinders.
• Compile executed validation packages.
• Support SOP development.
• Lead and write deviation investigations related to validations or assist in non-conformances/CAPA investigations.

Skills

Technical writing

Project coordination

Cross-functional communication

Detail orientation

Ability to manage priorities

Education

Bachelor’s degree in Life Sciences, Engineering or related

Job description

VTI Life Sciences (VTI) seeks a forward-thinking Medical Device Quality Engineer for a 4‑month contract in Pendleton, SC. The role focuses on leading validation execution activities with operations and engineering teams for special processes, including laser marking and laser welding.

The candidate will review IQ/OQ/PQ protocols, execute validation activities on manufacturing equipment, and contribute to SOP development.