Evening QC Analyst, cGMP & Stability Lab

Gannet BioChem; Huntsville (AL); On-site; USD 55,000 - 75,000; Full time

Job summary

Gannet BioChem is seeking a Quality Control laboratory professional for a second shift (4:00 pm–1:00 am, Sun–Thu) to support pharmaceutical CDMO testing and release. You will apply QC practices, data integrity, and cGMP/GLP standards to solve problems in a practical way.

You will prepare samples and run analytical tests (HPLC/UPLC, GC, UV-Vis, FTIR, titration, Karl Fischer, dissolution, wet chemistry), document results, and train other staff as needed.

Qualifications

• Bachelor's degree required in chemistry or a related field.
• Minimum two years of cGMP/cGLP experience.
• Experience in Quality Control, analytical testing, CDMO operations, or a regulated lab.
• Hands-on with analytical instrumentation (HPLC/UPLC, GC, UV-Vis, FTIR, titration, Karl Fischer, dissolution, wet chemistry).
• Ability to document data and maintain accurate records per SOPs.

Responsibilities

• Perform QC lab activities to support testing and client projects.
• Prepare samples, standards, reagents, buffers, and mobile phases per procedures.
• Execute analytical testing using validated methods (HPLC/UPLC, GC, UV-Vis, FTIR, etc.).
• Document observations, calculations, and results with accuracy.
• Train others on simple tasks and assist in method transfer.
• Collaborate with QA, Analytical Development, and manufacturing teams.

Skills

Quality Control

Analytical Testing

cGMP/GLP

Data Integrity

Laboratory Documentation

HPLC/UPLC

GC

UV-Vis

FTIR

Titration

Karl Fischer

Dissolution

Wet Chemistry

SOP Adherence

Team Collaboration

Education

Bachelor's degree in Chemistry/related Scientific Field

Tools

HPLC/UPLC

GC

UV-Vis

FTIR

Titration

Karl Fischer

Dissolution

Wet Chemistry

Job description

Gannet BioChem is seeking a Quality Control laboratory professional for a second shift (4:00 pm–1:00 am, Sun–Thu) to support pharmaceutical CDMO testing and release. You will apply QC practices, data integrity, and cGMP/GLP standards to solve problems in a practical way.

You will prepare samples and run analytical tests (HPLC/UPLC, GC, UV-Vis, FTIR, titration, Karl Fischer, dissolution, wet chemistry), document results, and train other staff as needed.