<p>Job Title: Sr. Biopharmaceutical Processing Technician</p> <p>Job Description</p> <p>This role supports the manufacture of Commercial and Clinical Biologics by performing operations in adherence to Current Good Manufacturing Practices (cGMPs). You will work with both Upstream (cell culture) and Downstream (chromatography) processes, contributing to the flawless execution of manufacturing batch records, work instructions, and SOPs. Your attention to detail will ensure tasks are completed correctly the first time, and you will assist in maintaining suite, supplies, equipment, logbooks, and data according to strict cGMP standards.</p> <p>Responsibilities</p> <ul> <li>Execute manufacturing batch records, work instructions, and SOPs with a focus on proactive 'right the first time' executions. </li><li>Assist with batch record reconciliation and all departmental functions including maintaining suite, supplies, equipment, logbooks, and data. </li><li>Document all activities to meet cGMP requirements and complete document reviews and revisions. </li><li>Participate in shift exchanges, 1-1 meetings, and other meetings as needed. </li><li>Support quality investigations by providing feedback and suggestions for improvement. </li><li>Adhere to safety procedures and promote safe work habits. </li><li>Critically evaluate processes, prioritize tasks according to production schedules, and manufacture buffers and simple bulk reagents. </li><li>Participate in process improvement projects. </li><li>Review all area documents and assist in the manufacture of controls and calibrators. </li><li>Perform in-process assays and product filtrations. </li><li>Clean and sterilize equipment, including using autoclaves. </li><li>Maintain lab equipment and monitor lab supplies. </li><li>Respond to emergency notifications and work flexible hours, including weekends. </li></ul> <p>Essential Skills</p> <ul> <li>Proficiency in cleanroom and aseptic techniques. </li><li>Experience in cell culture, chromatography, and biochemistry. </li><li>Knowledge of cGMP practices and chemical concepts. </li><li>Minimum of 2 years of experience in manufacturing, operation, production, or lab settings. </li><li>Bachelor's Degree in a STEM-related field preferred. </li></ul> <p>Additional Skills & Qualifications</p> <ul> <li>Experience in a cGMP environment is preferred. </li><li>Subject Matter Expert on upstream processing steps is advantageous. </li><li>Ability to lift a minimum of 25 lbs independently and stand for 80% of the shift. </li></ul> <p>Work Environment</p> <p>The position is based in a cleanroom/aseptic suite environment, requiring full gowning including bodysuit, gloves, hair & beard nets, face covers, and safety glasses. It operates on rotating 12-hour shifts, working 7 days out of a 2-week period, with both night and day shifts available. Employees must adhere to cleanroom gowning requirements and be able to work flexible hours, including weekends.</p> <p>Job Type & Location</p> <p>This is a Contract to Hire position based out of Saint Louis, MO.</p> <p>Pay and Benefits</p> <p>The pay range for this position is $28.00 - $28.00/hr.</p> <p>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:</p> <ul> <li>Medical, dental & vision </li><li>Critical Illness, Accident, and Hospital </li><li>401(k) Retirement Plan - Pre-tax and Roth post-tax contributions available </li><li>Life Insurance (Voluntary Life & AD&D for the employee and dependents) </li><li>Short and long-term disability </li><li>Health Spending Account (HSA) </li><li>Transportation benefits </li><li>Employee Assistance Program </li><li>Time Off/Leave (PTO, Vacation or Sick Leave) </li></ul> <p>Workplace Type</p> <p>This is a fully onsite position in Saint Louis,MO.</p> <p>Application Deadline</p> <p>This position is anticipated to close on Apr 13, 2026.</p> <p>Diversity, Equity & Inclusion</p> <p>At Actalent, diversity and inclusion are a bridge towards the equity and success of our people. DE&I is embedded into our culture through:</p> <ul> <li>Hiring diverse talent </li><li>Maintaining an inclusive environment through persistent self-reflection </li><li>Building a culture of care, engagement, and recognition with clear outcomes </li><li>Ensuring growth opportunities for our people </li></ul> <p>Actalent is an equal opportunity employer.</p> <p>About Actalent</p> <p>Actalent is a global leader in engineering and sciences services. For more than 40 years, we've helped visionary companies advance their goals. Headquartered in the United States, our teams span 150 offices across North America, EMEA, and APAC-with four delivery centers in India led by 1,000+ extraordinary employees who connect their passion with purpose every day.</p> <p>Our Bangalore, Hyderabad, Pune, and Chennai delivery centers are hubs of engineering expertise, with core capabilities in mechanical and electrical engineering, systems and software, and manufacturing engineering. Our teams deliver work across multiple industries including transportation, consumer and industrial products, and life sciences. We serve more than 4,500 clients, including many Fortune 500 brands. Learn more about how we can work together at actalentservices.com.</p>