• Sr. Biopharmaceutical Processing Technician

    Actalent (St. Louis, MO)


    Job Title: Sr. Biopharmaceutical Processing TechnicianJob Description

     

    As a Sr. Biopharmaceutical Processing Technician, you will support the manufacture of Commercial and Clinical Biologics by adhering to Current Good Manufacturing Practices (cGMPs) and performing various functions related to Upstream and Downstream processes. This role involves collaborating with a team of exceptional professionals to ensure flawless execution of manufacturing batch records, work instructions, and SOPs. Your attention to detail and proactive approach will be crucial in maintaining suite supplies, equipment, logbooks, and data to strict cGMP standards.

    Responsibilities

    + Execute manufacturing batch records, work instructions, and SOPs, focusing on proactive 'right the first time' executions.

    + Assist with batch record reconciliation and documentation of all activities to meet cGMP requirements.

    + Complete document reviews and revisions, perform daily record reviews, and maintain task databases.

    + Participate and lead in shift exchanges and meetings to address area needs based on changes.

    + Support quality investigations by answering questions, providing feedback, and suggesting improvements.

    + Practice and promote safe work habits, adhering to safety procedures and guidelines.

    + Critically evaluate processes, prioritizing tasks according to production schedules.

    + Manufacture buffers and simple bulk reagents per manufacturing procedures with limited supervision.

    + Engage in process improvement projects and perform in-process assays using various laboratory equipment.

    + Perform product filtrations, clean and steam steel tanks, and prepare glassware and tanks for sterilization.

    + Maintain lab equipment and monitor stocks of common lab supplies.

    + Keep department lead or manager updated on all issues and respond to emergency notifications.

    + Work flexible hours, including weekends, as required.

    Essential Skills

    + Minimum of 2 years of work experience in manufacturing, operation, production, lab setting, or related field.

    + Experience with cell culture, chromatography, and aseptic techniques.

    + Knowledge of cGMP practices and chemical concepts.

    + Bachelor's Degree in Science with focus on aseptic techniques, cell culturing, and biochemistry preferred.

    Additional Skills & Qualifications

    + Preferred: 6 months of experience in a GMP regulated environment.

    + Subject Matter Expert on upstream processing steps preferred.

    + Ability to perform in a cleanroom environment and adhere to gowning requirements.

    Work Environment

    The work is conducted in cleanroom/aseptic suites where full gowning, including bodysuit, gloves, hair & beard nets, face covers, and safety glasses, is required. The role involves rotating 12-hour shifts from 6:45 am to 6:45 pm, working 7 days out of a 2-week period. It is necessary to lift a minimum of 25 lbs independently and stand for 80% of the shift.

     

    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 $28.00 - $28.00/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 Nov 17, 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 [email protected] (%[email protected]) for other accommodation options.