Quality Control Analyst II: GMP/GLP Lab Excellence

Dechra Pharmaceuticals PLC; Fort Worth, Northern (TX, KY); Hybrid; USD 65,000 - 90,000; Full time

Job summary

Dechra Pharmaceuticals PLC in Fort Worth, TX, is looking for a QC Analyst II to support quality control within a cGMP framework, perform routine and non-routine laboratory testing, and help update SOPs to ensure compliant operations.

You will analyze materials across raw, in-process, and finished products, maintain instruments (HPLC/GC), contribute to investigations, train others, and help keep the laboratory inspection-ready with meticulous documentation and data integrity.

Qualifications

• Bachelor's degree in a scientific discipline (Pharmaceutical Sciences, Pharmacy, Chemistry, Biology or related).
• Minimum of 2 years' experience in a pharmaceutical GMP environment.
• Preferred: 5 years' experience in a GMP laboratory.
• Familiarity with GMP regulations applicable in the United States.
• Experience with HPLC and/or GC in a GMP lab.

Responsibilities

• Adheres to cGMP procedures and regulatory requirements.
• Analyze raw materials, intermediates, finished products and stability samples.
• Initiate LIRs, OOS, deviations and change controls.
• Maintain calibration and verification of laboratory equipment.
• Prepare investigations summaries and technical reports.
• Provide training to other analysts and support inspections.
• Document accurately to ensure Right-First-Time testing.

Skills

Attention to detail

Cross-functional collaboration

Problem solving

Communication

Microsoft Excel

Documentation accuracy

Education

Bachelor's degree in Pharmaceutical Sciences or related field

Tools

HPLC

GC

Job description

Dechra Pharmaceuticals PLC in Fort Worth, TX, is looking for a QC Analyst II to support quality control within a cGMP framework, perform routine and non-routine laboratory testing, and help update SOPs to ensure compliant operations.

You will analyze materials across raw, in-process, and finished products, maintain instruments (HPLC/GC), contribute to investigations, train others, and help keep the laboratory inspection-ready with meticulous documentation and data integrity.