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Lead QC Scientist

Job in Round Rock, Williamson County, Texas, 78682, USA
Listing for: Randstad USA
Full Time position
Listed on 2026-10-05
Job specializations:
  • Science
    Research Scientist, Medical Science, Data Scientist, Clinical Research
Salary/Wage Range or Industry Benchmark: 90000 - 130000 USD Yearly USD 90000.00 130000.00 YEAR
Job Description & How to Apply Below

*** THIS IS A 12-MONTH CONTRACT WITH POSSIBILITY OF EXTENSION***

Who We Are:

Millipore Sigma is a leader in the life sciences. We aim to solve the toughest problems in the industry by collaborating with the global scientific community, and through that help increase access to health for people everywhere. We provide scientists and engineers with best-in-class lab materials, technologies, and services. We are dedicated to making research and biotech production simpler, faster, and more successful.

At Millipore Sigma, we are with our customers at every step of the drug development process, shaping the possibilities for tomorrow.

Scope of Responsibility:

The Lead Scientist (Analytical) is responsible for performing analytical testing of finished products, raw materials, custom analytical services, and in-process samples. The Lead Scientist will use their experience and education to solve problems, optimize processes, develop new processes and methods, and assist in the development and analysis of new products. The Lead Scientist will also develop investigational strategies and participate in Out of Specification (OOS) investigations.

All work is to be performed accurately and in compliance with Millipore Sigma, Round Rock Quality and Safety policies.

Purpose of the Position:
  • Conduct work in a professional manner.
  • Undertake an expanding range of analytical analyses in support of Millipore Sigma catalog, custom and new products.
  • Lead or participate in technical problem solving, implementation of new processes and initiatives.
  • Complete laboratory maintenance and housekeeping activities efficiently and in accordance with safety and quality policies and procedures.
  • Complete laboratory equipment calibrations, verifications and maintenance activities on schedule with required documentation.
  • Train on and demonstrate understanding of multiple analytical techniques.
  • Participate in development of and demonstrate understanding of departmental goals.
  • Demonstrate understanding of interdepartmental and Millipore Sigma processes and quality systems.
  • Demonstrate an understanding of and work in accordance with Millipore Sigma’s safety policies.
  • Work in accordance with documentation, quality and process policies and procedures.
Essential Job Functions:
  • Perform analytical testing of finished products, raw materials, custom analytical projects, and in-process samples as directed in standard operating procedures and methods.
  • Develop and execute investigational strategies in OOS investigations and write OOS reports.
  • Lead or participate in method development.
  • Lead and participate in analytical method validations and technical studies.
  • Perform instrument qualifications and maintenance/troubleshooting of analytical instruments.
  • Lead or participate in improvement of processes, procedures and systems.
  • Document work in accordance with Millipore Sigma and regulatory requirements.
  • Maintain the QC Laboratory in a state of audit readiness that includes a clean and organized work environment.
  • Adhere to Millipore Sigma quality requirements and perform work in compliance with policies and procedures, including controlled substance requirements.
  • Perform Laboratory work in accordance with Millipore Sigma safety policies and procedures.
  • Actively improve and promote safety policies in the laboratory.
BASIC QUALIFICATIONS

Education:
  • BS or MS or PhD in chemistry or relevant life science related field.
Knowledge and

Skills:

Experience:
  • BS or MS will have 4+ years prior work experience in a related field
  • PhD and no prior work experience.
  • Knowledge of the ISO 9001, ISO 17025 and ISO 17034 requirements.
  • May have prior work experience in a GLP, GMP and/or ISO environment.
  • May have knowledge of quality system requirements of the medical device, pharmaceutical and/or…
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