QC Analyst II — Evening Shift (Pharma, cGMP)

Gannet BioChem; Huntsville (AL); On-site; USD 55,000 - 85,000; Full time

Job summary

Gannet BioChem in Huntsville, AL is seeking a QC Analyst to join a second-shift team supporting pharmaceutical CDMO testing and release. The role requires independence on routine tasks, strong data integrity, and collaboration with QA and manufacturing.

The position performs analyses including HPLC/UPLC, GC, UV‑Vis, FTIR, and dissolution while documenting results and ensuring compliance with cGMP/GLP procedures. Shift: 4:00 pm–1:00 am, Sunday–Thursday.

Qualifications

• Bachelor’s degree in Chemistry or related field required.
• 2+ years of cGMP/cGLP experience preferred.
• Strong documentation and data integrity skills.

Responsibilities

• Perform QC laboratory activities supporting CDMO testing and release.
• Apply cGMP/GLP practices and SOPs to solve problems.
• Prepare samples, reagents, and buffers according to procedures.
• Conduct analytical testing (HPLC/UPLC, GC, UV-Vis, FTIR, titration, dissolution).
• Document results and communicate findings to teams.

Job description

Gannet BioChem in Huntsville, AL is seeking a QC Analyst to join a second-shift team supporting pharmaceutical CDMO testing and release. The role requires independence on routine tasks, strong data integrity, and collaboration with QA and manufacturing.

The position performs analyses including HPLC/UPLC, GC, UV‑Vis, FTIR, and dissolution while documenting results and ensuring compliance with cGMP/GLP procedures. Shift: 4:00 pm–1:00 am, Sunday–Thursday.