QC Analytical Scientist
Job in
Austin, Travis County, Texas, 78716, USA
Listed on 2026-10-18
Listing for:
Trident Consulting
Full Time
position Listed on 2026-10-18
Job specializations:
-
Quality Assurance - QA/QC
Job Description & How to Apply Below
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.
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