Biomanufacturing Specialist

Think the best job opportunities are far away? Think again. Great opportunities are right here in your backyard. Kelly® is looking for a Manufacturing Specialist to work at a premier biotechnology organization in Houston, TX. Let us help you grow at work and discover the next step in your career, all while being a vital part of your community.

• Competitive pay rate with weekly pay options
• Opportunity to support groundbreaking gene therapy research and production
• Safe, clean, GMP-regulated manufacturing environment
• Work with cutting-edge bioprocessing technology and equipment
• Collaborative workplace culture with opportunities for skill development and advancement

• Operating manual, semi-automated, and automated equipment for the production of preclinical and clinical biopharmaceuticals
• Performing large-scale cell culture with single-use disposable bioreactor systems
• Conducting viral vector purification using process-scale chromatography equipment
• Preparing buffer solutions and staging equipment/raw materials in production suites
• Assisting with validation, data collection, inventory management, and equipment maintenance
• Cleaning facility and unit process equipment, and ensuring completion of proper documentation to meet quality system requirements
• Writing and reviewing SOPs and change control documents for manufacturing work areas
• Participating in facility safety programs and resolving technical problems with internal teams and external vendors

• Have a Bachelor’s degree in Biology, Biotechnology, or a related scientific field (required)
• Bring experience in biopharmaceutical manufacturing, ideally in a GMP-regulated environment (preferred but not required)
• Are skilled in upstream and/or downstream manufacturing processes, including cell culture, aseptic processing, biosafety cabinets, process-scale chromatography, buffer preparation, and viral vector manufacturing/purification
• Demonstrate understanding of cGMP requirements, deviation investigations, root cause analysis, CAPAs, and quality systems
• Have strong aseptic technique, attention to contamination control, and commitment to accurate documentation
• Are comfortable performing repetitive laboratory/manufacturing tasks and following written procedures
• Communicate and collaborate effectively across departments and levels
• Can troubleshoot routine technical issues and elevate appropriately
• Are physically able to work in a GMP cleanroom environment, follow gowning requirements, lift up to 50 lbs. with assistance, and consistently adhere to safety and environmental procedures