• QC Raw Materials Scientist III

    Actalent (St. Louis, MO)


    Job Title: QC Raw Materials Scientist IIIJob Description

     

    We are seeking a dedicated QC Raw Materials Scientist III to act as a Subject Matter Expert for compendial raw material HPLC method verification and SOP generation. Your role will be integral in ensuring laboratory safety and compliance with environmental health and safety (EHS) standards. You will conduct compendial GMP testing in an analytical laboratory environment, utilizing a variety of wet chemistry and equipment-based assays. Your keen attention to detail will help you recognize and report out-of-specification or out-of-trend results to laboratory management, and you will recommend solutions to rectify any issues.

    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.

    + Assure all activities meet EHS requirements.

    + Conduct compendial GMP testing in an analytical laboratory environment using a variety of wet chemistry and equipment-based assays.

    + 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 needed.

    + Author and/or review SOPs and test method forms in the document management system eDMS.

    + Perform all duties in compliance with Standard Operating Procedures, Good Manufacturing Practices, Good Laboratory Practices, and Safety guidelines.

    + Work with internal and external customers to ensure clear and open communication is maintained when resolving and raising issues.

    Essential Skills

    + Minimum of 5 years of pharmaceutical HPLC/UPLC experience.

    + Experience with compendial HPLC assays.

    + Knowledge of GMP regulations in a cGMP manufacturing environment.

    + Working knowledge of scientific principles for a wide range of analytical techniques.

    + Attention to detail and familiarity with compendia and USP methods.

    Additional Skills & Qualifications

    + BS Degree in a related field.

    + Prior use of EMPOWER is preferred.

    + Experience with ICP testing is preferred.

    + Experience in biopharmaceutical quality control.

    Work Environment

    The work schedule is Monday to Friday, from 8:00 am to 4:30 pm. The environment fosters impactful work, innovative thinking, and a customer-focused culture. You will be part of a fast-growing, global organization with a commitment to serving science and providing resources and opportunities for career growth. The role does not require weekend work.

     

    Job Type & Location

     

    This is a Contract to Hire position based out of Saint Louis, MO.

    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 Type

     

    This is a fully onsite position in Saint Louis,MO.

     

    Application Deadline

     

    This position is anticipated to close on Jan 3, 2026.

    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 [email protected] (%[email protected]) for other accommodation options.