QC Analytical Scientist

Trident Consulting; Austin (TX); On-site; USD 83,000 - 104,000; Full time

Job summary

Trident Consulting seeks a QC Lead Scientist for a 12-month engagement in Round Rock, TX. The role covers analytical testing of finished products, raw materials, and in-process samples, with responsibilities including method development, validation, OOS investigations, and ensuring GMP/GLP compliance.

Schedule is Monday–Friday, 8:00 AM–5:00 PM, paying $40–$50 per hour on a W2. Requirements include a BS/MS/PhD in Chemistry or Life Sciences and at least 4 years of relevant experience; PhD

Qualifications

• BS, MS, or PhD in Chemistry, Life Sciences, or a related field.
• 4+ years of relevant analytical experience for BS/MS; PhD considered entry level.
• Experience with analytical methods and result interpretation.
• Knowledge of ISO 9001, ISO 17025, ISO 17034; GMP/GLP/ISO environments preferred.
• Strong technical writing and communication skills.

Responsibilities

• Perform analytical testing of finished products, raw materials, and in-process samples.
• Lead or participate in analytical method development and validation.
• Develop and execute OOS investigations and reports.
• Maintain GMP/GLP/ISO compliance and audit readiness.
• Document procedures, reports, and training materials.

Skills

Analytical methods

Data interpretation

Technical writing

Communication skills

GMP/GLP/ISO

Laboratory testing

Education

BS in Chemistry or Life Sciences

MS in Chemistry or Life Sciences

PhD in Chemistry or Life Sciences

Job description

Trident Consulting is seeking a \" QC Lead Scientist \" for one of our clients in \"Round Rock, TX ” A global leader in business and technology services.

Job Title: QC Lead Scientist / Lead Scientist – Analytical

Duration: 12 months, with potential

Schedule: Monday–Friday, 8:00 AM–5:00 PM

Pay Rate: $40–$50/hour W2

Position Summary:

Seeking a QC Lead Scientist to perform analytical testing of finished products, raw materials, custom analytical projects, and in-process samples. The role will support method development, method validation, OOS investigations, technical troubleshooting, and laboratory quality activities in a regulated environment.

Key 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.


• Work safely with hazardous chemicals and required laboratory PPE.

Basic Qualifications:

• BS, MS, or PhD in Chemistry, Life Sciences, or a related field.


• BS/MS: 4+ years of relevant experience.


• PhD: Entry-level candidates may be considered.


• Experience with analytical methods and interpretation of analytical 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.