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QC Analytical Scientist

Job in Austin, Travis County, Texas, 78716, USA
Listing for: Trident Consulting
Full Time position
Listed on 2026-10-18
Job specializations:
  • Quality Assurance - QA/QC
Salary/Wage Range or Industry Benchmark: 40 - 50 USD Hourly USD 40.00 50.00 HOUR
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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