Qualification documentation jobs

Quality Engineer

LifeSprout · Posted Nov 5, 2026

Baltimore, Maryland, United States
On-site
Temporary · Senior
5+ years

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The Quality Engineer provides hands-on Quality Assurance and Quality Systems support for LifeSprout’s medical-device development, manufacturing, and related operations.

Responsibilities

Provide hands-on Quality Assurance support for manufacturing, engineering, development, and QMS activities.
Support deviations, nonconformances, CAPAs, change controls, document control, training, and supplier quality activities.
Review and approve controlled documents, batch records, protocols, validation/qualification documentation, investigations, and reports.
Support material and product disposition, release activities, and management of nonconforming materials.
Support process validation, equipment qualification, design controls, and risk management activities.

Requirements

Bachelor’s degree in engineering
Life Sciences
another relevant scientific or technical discipline
Nice to have: EU MDR
Nice to have: ISO 14971

Skills

ISO 13485 FDA medical-device Quality System requirements CAPA deviations

Global Engineering Advisor – Facilities & Utilities

Global Engineering Advisor – Facilities & Utilities

Responsibilities

Requirements

Skills

Benefits

Quality Engineer

Responsibilities

Requirements

Skills