US - Quality Control Expert 3

The Fountain Group; Round Rock (TX); On-site; USD 55,000 - 69,000; Full time

Job summary

The Fountain Group is seeking a QC Lead Scientist (Analytical) for a prominent client in Round Rock, Texas. The role focuses on analytical testing of finished products, raw materials, and in-process samples, with day-to-day oversight of QC analysts on-site.

You will lead investigations, develop analytical methods, qualification and calibration of instruments, and ensure compliance with ISO 9001/17025/17034, GMP/GLP where applicable.

Qualifications

• Bachelor's or higher in chemistry or life sciences and 4+ years of relevant experience (PhD candidates may qualify without prior work experience).
• Hands-on analytical testing and interpretation of analytical results.
• Experience leading 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.

Responsibilities

• 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 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.

Skills

Analytical testing

OOS investigations

Method development

Instrument calibration

Technical report writing

ISO/regulatory knowledge

Education

Bachelor's/Master's/PhD in Chemistry or Life Sciences

Job description

The Fountain Group iscurrently 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

Job Description

• 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, 8:0 AM–5:00 PM, with appropriate PPE when handling hazardous chemicals.

Education

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

Required Skills

• 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.

Preferred Skills

• 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.