QC Scientist

Trident Consulting•Round Rock, TX

About The Position

The QC Scientist (Analytical) performs analytical testing of finished products, raw materials, custom analytical services, and in-process samples. The role uses scientific experience and education to solve problems, optimize and develop processes and methods, and assist in developing and analyzing new products. The Scientist also develops investigational strategies and participates in Out of Specification (OOS) investigations. All work must be performed accurately and in compliance with MilliporeSigma, Round Rock Quality, and Safety policies. The position is based in Round Rock, Texas, and is a 12-month contract with potential to become permanent. The stated schedule is Monday through Friday, 8 a.m. to 5 p.m.; a move to a second shift (12 p.m. to 9 p.m.) may occur later, but that shift has not been approved.

Requirements

  • Bachelor's or master's degree in chemistry or a relevant life science-related field.
  • At least 2 years of prior work experience in a related field for candidates with a bachelor's or master's degree.
  • At least 2 years of industry experience.
  • Experience with chromatography, including HPLC and GC.
  • Knowledge of ISO 9001, ISO 17025, and ISO 17034 requirements.
  • Demonstrated knowledge and experience in analytical methods and interpretation of analytical results.
  • Excellent verbal and technical writing skills.
  • Understanding of MilliporeSigma products, their applications, and requirements.

Nice To Haves

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

Responsibilities

  • Perform analytical testing of finished products, raw materials, custom analytical services, and in-process samples.
  • Solve problems and optimize processes using relevant experience and education.
  • Develop new processes and methods.
  • Assist in the development and analysis of new products.
  • Develop investigational strategies and participate in Out of Specification (OOS) investigations.
  • Perform work accurately and in compliance with MilliporeSigma, Round Rock Quality, and Safety policies.
  • Write procedures, reports, OOS reports, training documents, and technical presentations.
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