QC Chemist I: GMP Lab Analyst — Growth & Training

Sovereign Pharmaceuticals; Fort Worth (TX); On-site; USD 42,000 - 64,000; Full time

Job summary

Sovereign Pharmaceuticals in Fort Worth, TX is seeking a QC Chemist I to perform qualitative and quantitative analyses on raw materials, packaging components, and finished drug products, including stability testing, to support high‑volume manufacturing. Under direct supervision, you will follow USP testing methods, GDP, and cGMP, develop written documentation, and maintain data integrity.

Requires an associate or bachelor’s degree in chemistry with 1–4 years of experience and strong

Qualifications

• Intermediate Excel skills preferred but not required.
• Professional demeanor
• Reliable and dependable
• Organized and detail-oriented
• Highly accurate and efficient
• Exercises confidentiality
• Strong communication skills

Responsibilities

• Follows test methods and completes testing with supervision.
• Learns and applies USP concepts for laboratory testing.
• Develops oral and written communication skills.
• Follows GDP for all documentation.
• Demonstrates basic lab skills and equipment understanding.
• Learns and follows cGMP, DEA regulations, and quality procedures.
• Compiles results and understands data integrity concepts.
• Identifies basic problems and seeks assistance.
• Uses sound scientific principles and understanding of instruments.
• Technical support with supervision; assists with cleanup and maintenance; understands GDP and 2PV requirements.
• Orders materials under supervision; pursues self-improvement; documents activities; demonstrates data ethics.
• Works under direct supervision.

Skills

Excel (intermediate)

Professional demeanor

Reliable and dependable

Organized and detail‑oriented

Highly accurate and efficient

Confidentiality

Strong communication skills

Education

Associate degree in Chemistry

Bachelor's degree in related scientific field

BA or BS in Chemistry

Job description

Sovereign Pharmaceuticals in Fort Worth, TX is seeking a QC Chemist I to perform qualitative and quantitative analyses on raw materials, packaging components, and finished drug products, including stability testing, to support high‑volume manufacturing. Under direct supervision, you will follow USP testing methods, GDP, and cGMP, develop written documentation, and maintain data integrity.

Requires an associate or bachelor’s degree in chemistry with 1–4 years of experience and strong