Analytical QC Lead Scientist – Method Development & GMP

Trident Consulting; Austin (TX); On-site; USD 55,000 - 69,000; Full time

Job summary

Trident Consulting is seeking a QC Lead Scientist in Round Rock, TX to perform analytical testing of finished products, raw materials, and in-process samples. The role supports method development, method validation, OOS investigations, and lab quality activities in a regulated environment.

Duration is 12 months with a typical 8:00 AM–5:00 PM schedule. Responsibilities include leading analytical method development/validation, conducting instrument qualification, maintaining audit-ready QC labs,

Qualifications

• BS/MS: 4+ years of relevant experience.
• PhD: Entry-level candidates may be considered.
• Experience with analytical methods and interpretation of results.
• Knowledge of ISO 9001, ISO 17025, and ISO 17034.
• Experience in GMP, GLP, and/or ISO environments preferred.
• Knowledge of pharmaceutical, medical device, or clinical quality systems preferred.
• Strong technical writing and communication skills.

Responsibilities

• Perform analytical testing of finished products, raw materials, and in-process samples.
• Develop and execute OOS investigations and prepare OOS reports.
• Lead or participate in analytical method development and validation.
• Perform instrument qualification, maintenance, and troubleshooting.
• Support technical studies and process improvements.
• Maintain accurate documentation in compliance with regulatory requirements.
• Maintain the QC laboratory in an audit-ready condition.
• Support equipment calibration and verification activities.
• Follow GMP/GLP, ISO, quality, and safety procedures.
• Prepare procedures, technical reports, training documents, and presentations.

Skills

Analytical testing

OOS investigations

Method development

Method validation

Instrument maintenance

Education

BS/MS/PhD in Chemistry or Life Sciences

Job description

Trident Consulting is seeking a QC Lead Scientist in Round Rock, TX to perform analytical testing of finished products, raw materials, and in-process samples. The role supports method development, method validation, OOS investigations, and lab quality activities in a regulated environment.

Duration is 12 months with a typical 8:00 AM–5:00 PM schedule. Responsibilities include leading analytical method development/validation, conducting instrument qualification, maintaining audit-ready QC labs,