QC Raw Materials Scientist III

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Job Title: QC Raw Materials Scientist III
Job Description
Join our dynamic team as a QC Raw Materials Scientist III, where you will serve as a Subject Matter Expert for compendial raw material HPLC method verification and SOP generation. Your role will be crucial in ensuring the quality and safety of pharmaceutical products by conducting compendial GMP testing in an analytical laboratory environment. You will uphold laboratory safety standards and maintain a high level of quality control.
Responsibilities

• Act as a Subject Matter Expert for compendial raw material HPLC method verification and SOP generation.
• Demonstrate proper laboratory safety and housekeeping practices through weekly 5S Lab audits and monthly laboratory inspections.
• Ensure all activities meet Environmental, Health, and Safety (EHS) requirements.
• Conduct compendial GMP testing using a variety of wet chemistry and equipment-based assays according to lab procedures and quality systems.
• Recognize and report out-of-specification/out-of-trend results to laboratory management and recommend solutions.
• Maintain and troubleshoot analytical instrumentation and workspace as needed.
• Perform method validation and/or qualification testing as required.
• Author and/or review Standard Operating Procedures (SOPs) and test method forms in the document management system (eDMS).
• Perform all duties in compliance with Standard Operating Procedures, Good Manufacturing Practices (GMP), Good Laboratory Practices (GLP), and safety guidelines.
• Work with internal and external customers to ensure clear and open communication when resolving and raising issues.
  

Essential Skills

• Bachelor's degree with 5 years of experience in HPLC and compendia (wet chemistry USP methods).
• Strong attention to detail.
• Experience in quality control and laboratory environments.
• Knowledge of GMP regulations in a cGMP manufacturing environment.
• Working knowledge of scientific principles for a wide range of analytical techniques.
  

Additional Skills & Qualifications

• Experience with compendial HPLC assays is a plus.
• Prior use of EMPOWER is preferred.
• Experience with ICP testing is preferred.
  

Work EnvironmentWork hours are Monday to Friday, 8:00 AM to 4:30 PM. This role does not require weekend shifts. You will be part of a team dedicated to impactful work, such as helping find cures for cancer and ensuring food safety. The organization values innovative thinking and provides resources for career growth in a fast-growing, global environment.Job Type & Location
This is a Contract to Hire position based out of Saint Louis, Missouri.
Pay and Benefits
The pay range for this position is $38.00 - $43.00/hr.
Eligibility requirements apply to some benefits and may depend on your job
classification and length of employment. Benefits are subject to change and may be
subject to specific elections, plan, or program terms. If eligible, the benefits
Available For This Temporary Role May Include The Following

• Medical, dental & vision
• Critical Illness, Accident, and Hospital
• 401(k) Retirement Plan – Pre-tax and Roth post-tax contributions available
• Life Insurance (Voluntary Life & AD&D for the employee and dependents)
• Short and long-term disability
• Health Spending Account (HSA)
• Transportation benefits
• Employee Assistance Program
• Time Off/Leave (PTO, Vacation or Sick Leave)
  

Workplace TypeThis is a fully onsite position in Saint Louis,MO.Application Deadline
This position is anticipated to close on Sep 2, 2025.
About Actalent
Actalent is a global leader in engineering and sciences services and talent solutions. We help visionary companies advance their engineering and science initiatives through access to specialized experts who drive scale, innovation and speed to market. With a network of almost 30,000 consultants and more than 4,500 clients across the U.S., Canada, Asia and Europe, Actalent serves many of the Fortune 500.
The company is an equal opportunity employer and will consider all applications without regard to race, sex, age, color, religion, national origin, veteran status, disability, sexual orientation, gender identity, genetic information or any characteristic protected by law.
If you would like to request a reasonable accommodation, such as the modification or adjustment of the job application process or interviewing due to a disability, please email for other accommodation options.

Seniority level

• Seniority level

  Mid-Senior level

Employment type

• Employment type

  Contract

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• Job function

  Research, Analyst, and Information Technology

• Industries

  Business Consulting and Services

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