US - Quality Control Expert 3

The Fountain Group is currently seeking a QC Lead Scientist (Analytical) for a prominent client of ours. This position is located at Round Rock, TX. Details for the position are as follows:

QC Lead Scientist (Analytical)
Location: Round Rock, TX
Pay Rate: $40–$50/hr, depending on experience
Duration: 12 months, with potential for temp-to-perm conversion

• Perform analytical testing of finished products, raw materials, custom analytical projects, and in-process samples.

• Lead technical investigations, troubleshoot complex analytical issues, and develop strategies for Out-of-Specification (OOS) investigations.

• Develop, validate, and optimize analytical methods and testing procedures.

• Lead technical studies and process improvement initiatives.

• Perform analytical instrument qualification, calibration, maintenance, and troubleshooting.

• Prepare OOS investigation reports, technical reports, procedures, and controlled laboratory documentation.

• Maintain laboratory audit readiness and ensure compliance with quality systems, regulatory requirements, and laboratory safety procedures.

• Provide technical guidance and training to QC analysts.

• Work onsite Monday–Friday, 8:00 AM–5:00 PM, with appropriate PPE when handling hazardous chemicals.

• Bachelor's, Master's, or PhD in Chemistry or a related Life Sciences field.

• Bachelor's or Master's degree with 4+ years of relevant experience; PhD candidates may qualify without prior work experience.

• Hands-on analytical testing and interpretation of analytical results.

• Experience leading technical investigations, troubleshooting analytical methods, and resolving complex laboratory issues.

• Experience with OOS investigations, investigation strategies, and report writing.

• Analytical method development, validation, and technical studies.

• Analytical instrument qualification, calibration, maintenance, and troubleshooting.

• Knowledge of ISO 9001, ISO 17025, and ISO 17034 requirements.

• Technical documentation, including SOPs, OOS reports, validation reports, and laboratory procedures.

• Experience in GLP, GMP, or ISO-regulated laboratory environments.

• Experience in pharmaceutical, medical device, clinical, or chemical manufacturing industries.

• Knowledge of QC quality systems, regulatory compliance, and audit readiness.

• Experience providing technical guidance and training to laboratory analysts.

• Familiarity with hazardous chemical handling and laboratory safety requirements.
   

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