QC Chemist II: Method Development & Instrument Validation

Fusion Life Sciences; Johns (WV, AL); On-site; USD 75,000 - 105,000; Full time

Job summary

Fusion Life Sciences is seeking a Quality Control Chemist II to support analytical chemistry in a regulated manufacturing setting. You will develop and validate methods, qualify instruments, and troubleshoot laboratory systems to ensure compliant, reliable results.

The role collaborates with QC, Manufacturing, and QA, and requires hands-on experience in method development, validation, and instrument qualification within a GMP/GLP-regulated environment.

Qualifications

• Bachelor's degree in Chemistry or related field is required.
• Experience with analytical method validation and instrument qualification.
• Strong communication and cross-functional collaboration skills.

Responsibilities

• Develop, optimize and improve analytical test methods for lab and manufacturing needs.
• Execute analytical method validations, transfers and periodic reviews per procedures.
• Support method transfers between internal sites and external suppliers.
• Perform compendial assessments and evaluate changes to requirements.
• Execute instrument qualifications and lifecycle activities; provide troubleshooting.
• Lead complex technical projects and drive timely delivery.
• Support investigations, CAPA and technical documentation review.
• Collaborate with cross-functional teams to meet timelines and quality.

Skills

Analytical method development

Analytical method validation

Instrument qualification

Cross-functional collaboration

Regulated environment

Education

Bachelor's degree in Chemistry or related field

Master's or Ph.D. preferred

Tools

LabVantage LIMS

Empower 3

Microsoft Office

Job description

Fusion Life Sciences is seeking a Quality Control Chemist II to support analytical chemistry in a regulated manufacturing setting. You will develop and validate methods, qualify instruments, and troubleshoot laboratory systems to ensure compliant, reliable results.

The role collaborates with QC, Manufacturing, and QA, and requires hands-on experience in method development, validation, and instrument qualification within a GMP/GLP-regulated environment.