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Job description
QC Lead Scientist
Location: Round Rock, TX
Pay Rate: $40–$50/hour
Duration: 12 months, with potential temp-to-perm conversion
Schedule: Monday–Friday, 8:00 AM–5:00 PM
Work Arrangement: 100% On-site
Openings: 2
Job Description
Perform analytical testing of finished products, raw materials, in-process samples, and custom analytical projects.
Develop and execute investigational strategies for Out of Specification (OOS) investigations and prepare OOS reports.
Lead or participate in analytical method development, validation, and technical studies.
Perform instrument qualification, calibration, maintenance, troubleshooting, and verification.
Support process, procedure, and laboratory system improvements.
Maintain QC laboratory readiness in accordance with applicable quality and regulatory requirements.
Prepare and maintain SOPs, technical reports, OOS documentation, training materials, and analytical records.
Perform laboratory activities in compliance with GMP, GLP, ISO, safety, and controlled-substance requirements.
Work with hazardous chemicals, including flammable solvents, carcinogens, dioxins, and corrosive materials, while following required laboratory PPE procedures.
Education
BS, MS, or PhD in Chemistry or a related Life Science field.
BS/MS: 4+ years of related analytical laboratory experience.
PhD: Prior work experience not required.
Required Skills
Analytical testing and interpretation of analytical results.
Analytical method development and validation.
OOS investigation and root-cause investigation strategies.
Analytical instrument qualification, calibration, maintenance, and troubleshooting.
Experience working with finished products, raw materials, and in-process samples.
GMP and/or GLP laboratory experience.
Knowledge of ISO 9001, ISO 17025, and ISO 17034 requirements.
QC documentation, SOPs, analytical reports, and technical documentation.
Laboratory quality systems and regulatory compliance.
Experience working with hazardous chemicals and laboratory PPE requirements.
Preferred Skills
Experience in pharmaceutical, medical device, or clinical laboratory environments.
Experience supporting ISO-regulated QC laboratories.
Knowledge of products, applications, and quality systems.
Experience with controlled-substance laboratory requirements.
Experience leading technical studies and laboratory process improvements.
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Worksite address
round rock, TX, 78682, US
Who can apply
Review the original listing for work authorization, qualifications and employer requirements.