Sr. Biopharmaceutical Processing Technician
6 days ago
Saint Louis
Job DescriptionJob Title: Senior Biopharmaceutical Processing Technician Job Description The Senior Biopharmaceutical Processing Technician supports the commercial and clinical manufacture of biologic products on a large scale, with a primary focus on upstream (cell culture) operations. Working in a cGMP-regulated cleanroom environment, this role performs aseptic cell culture activities, operates large-scale production bioreactors ranging from 50L to 2000L, and conducts large-scale filtration and centrifugation. The technician contributes directly to producing biologics used in pharmaceutical products, providing an excellent opportunity to gain experience in large-scale biological and chemistry-based pharmaceutical operations. Responsibilities • Execute manufacturing batch records, work instructions, and standard operating procedures (SOPs) with a strong focus on proactive, “right the first time” performance., • Assist with batch record reconciliation to ensure complete and accurate documentation of production activities., • Support all department functions, including maintaining production suites, supplies, equipment, logbooks, and data in accordance with site SOPs and policies., • Document all activities in compliance with cGMP requirements, ensuring timely and accurate entries., • Complete document reviews and revisions, including daily record review, task tracking, and database updates., • Participate and, when needed, lead shift exchanges, one-on-one discussions, and team meetings to communicate status updates and support area needs., • Engage in continuous improvement and lean activities to enhance operational efficiency and quality., • Support quality investigations by providing clear, accurate information and offering suggestions for process and documentation improvements., • Promote and follow safe work habits, adhering to all safety procedures and guidelines within the manufacturing and cleanroom environment., • Critically evaluate processes, demonstrating foresight and the ability to anticipate potential issues before they occur., • Interpret production schedules and prioritize tasks accordingly to meet manufacturing timelines and output goals., • Perform aseptic cell culture operations, including propagation of mammalian cell lines under controlled conditions., • Operate and monitor large-scale production bioreactors (50L–2000L) and related upstream processing equipment., • Conduct large-scale filtration and centrifugation steps as part of upstream bioprocessing workflows., • Apply aseptic technique consistently to maintain product quality and prevent contamination in cleanroom and aseptic suites.Essential Skills, • Minimum of 2 years of work experience in manufacturing, operations, production, laboratory setting, or a related field., • High school diploma or equivalent., • Ability to work in a cGMP-regulated environment and follow detailed procedures and documentation requirements., • Strong understanding of basic math to support accurate calculations and measurements in a manufacturing or laboratory context., • Proficiency with MS Office applications for documentation, data entry, and communication., • Demonstrated critical thinking and problem-solving skills, with the ability to recognize problems developing, not just occurring., • Ability to demonstrate practical knowledge with successful outcomes in a manufacturing or laboratory environment., • Ability to read, write, and communicate effectively in English., • Ability to understand and carry out written and verbal instructions accurately., • Capability to wear full cleanroom gowning, including bodysuit, gloves, hair and beard nets, face covers, and safety glasses, and to comply with restrictions on personal items and products., • Ability to meet cleanroom gowning requirements, including the use of Tyvek garments and Nitrile and/or Latex gloves., • Ability to lift a minimum of 25 pounds independently., • Ability to stand for approximately 80% of the work shift., • Willingness and ability to work rotating 12-hour shifts, including day or night shifts and alternating weekends.Additional Skills & Qualifications, • Bachelor’s degree in a STEM-related field, such as biology, chemistry, biochemistry, pharmaceutical sciences, or a related discipline, preferred., • Experience in a cGMP environment, preferred., • Knowledge of cGMP practices, aseptic techniques, or chemical concepts, preferred., • Subject matter expertise in upstream processing steps, preferred., • Experience with aseptic technique, cell culturing, and pipetting in a laboratory or production setting., • Experience working with bioreactors and upstream bioprocessing equipment., • Familiarity with chromatography, biochemistry, and pharmaceutical or biopharmaceutical industry processes., • At least 6 months of experience in a GMP-regulated environment with aseptic technique, preferred., • Background in cleanroom operations, aseptic suites, or other controlled environments., • Strong attention to detail and commitment to maintaining high-quality standards in documentation and operations.Work Environment This role operates in a cleanroom and aseptic suite environment that requires strict adherence to gowning and contamination-control procedures. Team members must be willing to fully gown up, including wearing a bodysuit, gloves, hair and beard nets, face covers, safety glasses, and Tyvek garments, along with Nitrile and/or Latex gloves. To maintain cleanroom standards, items such as makeup, jewelry, nail polish, cologne or perfume, and scented lotions or hair care products are not permitted in the production areas. The position involves standing for approximately 80% of the shift and lifting at least 25 pounds independently as part of routine operations. Work is performed on rotating 12-hour shifts, either day shift (6:45 a.m. to 6:45 p.m.) or night shift (6:45 p.m. to 6:45 a.m.), with a schedule that typically includes working 7 days over a 2-week period. An example rotation includes working Monday–Tuesday, off Wednesday–Thursday, and working Friday–Sunday in Week 1, followed by off Monday–Tuesday, working Wednesday–Thursday, and off Friday–Sunday in Week 2. The environment is highly regulated, team-oriented, and focused on producing biologics that support large-scale pharmaceutical products, offering exposure to advanced bioprocessing technologies and large-scale biological and chemistry operations. 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 • Hiring diverse talent, • Maintaining an inclusive environment through persistent self-reflection, • Building a culture of care, engagement, and recognition with clear outcomes 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.