QC Chemist I

Avion PharmaceuticalsFort Worth, TX
Onsite

About The Position

The primary function of a QC Chemist I is to perform qualitative and quantitative chemical and physical analyses at a high level in support of one of the following areas: Analysis of raw materials and packaging components, Analysis of in-process and finished drug products, including stability testing, for primarily high-volume products. This role operates in a professional laboratory and office environment. The employee is occasionally exposed to toxic and/or caustic chemicals such as sodium hydroxide, hydrochloric acid, acetonitrile, methanol, and other chemical solutions necessary in analytical chemistry. As a result, the employee may be required to wear a respirator or appropriate personal protective equipment (PPE) for certain laboratory tasks to ensure safety and protection. If a respirator is required, it will be provided by the company at no expense to the employee. In addition, any medical expenses for respirator fit testing will be covered by the employer.

Requirements

  • Associate degree in Chemistry with 2–4 years of experience
  • Bachelor's degree in a related scientific field with 1–2 years of experience
  • B.A. or B.S. in Chemistry
  • Ability to stay current with relevant technology
  • 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 as needed.
  • Learns and applies USP concepts for laboratory testing.
  • Develops oral and written communication skills.
  • Follows Good Documentation Practices (GDP) for all documentation.
  • Demonstrates basic laboratory skills and a foundational understanding of chemical testing equipment and processes.
  • Learns and follows basic cGMP (current Good Manufacturing Practices), DEA (Drug Enforcement Administration) regulations, and quality procedures for working in a QC laboratory.
  • Compiles results as directed and understands basic concepts related to the evaluation of analytical data and data integrity.
  • Identifies basic technical problems and seeks assistance when needed.
  • Uses sound scientific principles and demonstrates a basic understanding of laboratory instruments and equipment.
  • Performs testing with supervision as needed.
  • Assists with cleanup and maintenance of instrumentation.
  • Understands GDP and 2PV requirements for documentation review.
  • Orders materials as needed with supervision.
  • Recognizes deficiencies in foundational areas and pursues self-improvement.
  • Documents activities in procedures and laboratory notebooks with supervision.
  • Demonstrates declarative and procedural knowledge of data integrity and ethics.
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