QC Titration Scientist

job summary:
If you want real bench ownership where your analytical expertise directly drives product release, this role puts you at the heart of ISO-accredited quality control. Rather than running simple routine tests, you will operate automated titrators and advanced chromatography systems, troubleshoot complex OOS investigations, and help transfer cutting-edge analytical methods to market.

location: Round Rock, Texas
job type: Contract
salary: $30 - 38 per hour
work hours: 9 to 5
education: Bachelors

responsibilities:

• Perform analytical release testing (titration, HPLC, GC) for raw materials, finished products, in-process samples, and ongoing stability studies.
• Operate automated/manual titrators and chromatographic detectors including UV-Vis, RI, ELSD, and FID.
• Maintain laboratory notebooks, logbooks, and batch records while authoring technical reports, method documentation, test specifications, and OOS investigation strategies.
• Support analytical method development, validation, and technical transfers, actively participating in training colleagues on new technical workflows and procedures.
• Perform routine equipment qualifications, preventative maintenance, and troubleshooting across analytical lab instrumentation.
• Proactively communicate project status, schedule updates, planning risks, and resource requirements to managers and project teams to prevent operational delays.

 
qualifications:
Required:

• BS or MS in chemistry or relevant life science related field.

• 2+ years prior work experience in a related field.
• Prior experience performing titration, HPLC and GC.
• Knowledge of the ISO 9001, ISO 17025 and ISO 17034 requirements.

• The Scientist has demonstrated knowledge and experience in analytical methods and interpretation of analytical results.
• Ability to write procedures, reports, OOS reports, training documents, technical presentations, etc.

Preferred:

• Prior work experience in a GLP, GMP and/or ISO environment.
• Prior knowledge of quality system requirements of the medical device, pharmaceutical and/or clinical industries.

#LI-KH1

skills: High Pressure Liquid Chromatography (HPLC), Good Laboratory Practices (GLP), Good Manufacturing Practices (GMP), Quality Control (QC)


Equal Opportunity Employer: Race, Color, Religion, Sex, Sexual Orientation, Gender Identity, National Origin, Age, Genetic Information, Disability, Protected Veteran Status, or any other legally protected group status.

At Randstad, we welcome people of all abilities and want to ensure that our hiring and interview process meets the needs of all applicants. If you require a reasonable accommodation to make your application or interview experience a great one, please contact View email address on randstadusa.com.


Pay offered to a successful candidate will be based on several factors including the candidate's education, work experience, work location, specific job duties, certifications, etc. In addition, Randstad offers a comprehensive benefits package, including: medical, prescription, dental, vision, AD&D, and life insurance offerings, short-term disability, and a 401K plan (all benefits are based on eligibility).


This posting is open for thirty (30) days.