Overview
QC Validation Specialist Jobs in North Carolina, United States at Blackfield Associates
Title: QC Validation Specialist
Company: Blackfield Associates
Location: North Carolina, United States
QC Validation Specialist – Contract
Summary
Seeking QC Validation Specialists to support qualification and validation activities for QC laboratory and warehouse/interlogistics equipment within a pharmaceutical GMP environment.
Responsibilities
- Execute equipment qualification and validation activities
- Write, review, and execute IQ/OQ/PQ protocols and reports
- Support change controls and maintain validated state of equipment
- Coordinate with QA, IT, Metrology, and project stakeholders
- Support equipment release and project deliverables
Equipment Experience
Experience with QC laboratory equipment such as HPLC/UPLC, FTIR/NIR, Raman, TOC analyzers, particle size analyzers, refrigerators/freezers, balances, pipettes, water systems, and other benchtop instruments preferred.
Requirements
- Bachelor’s degree in Life Sciences, Chemistry, Engineering, or related field
- 2+ years of pharmaceutical validation, laboratory, or engineering experience
- Experience writing and executing validation protocols
- Working knowledge of GMP requirements
- Experience with TIMS and SAP PM/QM is a plus
- Strong technical writing and communication skills
Details
- 24-month contract
- Full-time, on-site role
- Monday–Friday | 8 AM – 5 PM EST
- Travel may be required for project support
