GMP Lab Quality Control Analyst I

Tevapharm; Cincinnati (OH); On-site; USD 65,000 - 90,000; Full time

Benefits offered by this job

Health Insurance

401(k) match

Paid Time Off

Life Insurance

Job summary

Teva Pharmaceuticals USA is seeking a Laboratory Analyst to perform routine and non-routine chemical testing of commercial, validation and stability samples using HPLC, GC, UV/Vis, KF and FTIR. You will work with LIMS and Empower to acquire and process data, analyze against specifications, and report OOS results.

The role requires a Bachelor’s in a science field (Chemistry preferred) and experience in a cGMP laboratory, with strong documentation and collaboration within a team to ensure Right

Qualifications

• Bachelor's in science related discipline (Chemistry preferred).
• Experience in a cGMP laboratory.
• Knowledge of USP, cGMP, and FDA regulations.

Responsibilities

• Perform routine and non-routine chemical testing of commercial, validation and stability samples.
• Analyze data against approved specifications and report OOS events.
• Maintain lab records and documentation per GMP/GLP.
• Troubleshoot instruments and methods; contribute to root cause investigations.

Skills

Analytical testing

HPLC

GC

UV/Vis

KF

FTIR

LIMS

Empower

Data analysis

GMP knowledge

cGMP

FDA regulations

Team collaboration

Problem solving

Documentation

Education

Bachelor's in science (Chemistry preferred)

Tools

LIMS

Empower

Job description

Teva Pharmaceuticals USA is seeking a Laboratory Analyst to perform routine and non-routine chemical testing of commercial, validation and stability samples using HPLC, GC, UV/Vis, KF and FTIR. You will work with LIMS and Empower to acquire and process data, analyze against specifications, and report OOS results.

The role requires a Bachelor’s in a science field (Chemistry preferred) and experience in a cGMP laboratory, with strong documentation and collaboration within a team to ensure Right