Key Responsibilities: Execute manufacturing activities following approved batch records and SOPs Operate and monitor automated cell processing, cell expansion, and fill/finish equipment Perform aseptic processing in Grade B/C cleanroom environments Complete GMP documentation accurately and in real time Support equipment cleaning, preparation, and routine maintenance Troubleshoot process or equipment issues and escalate appropriately Collaborate with QA, QC, Materials Management, and Manufacturing teams Assist with deviations, investigations, and continuous improvement initiatives Maintain compliance with cGMP, GDP, and safety requirements Key Requirements and Technology Experience: This role is ideal for candidates with experience in: GMP manufacturing Biopharmaceutical production Cleanroom operations Aseptic processing Batch record execution High School Diploma + 1+ year related GMP/manufacturing experience OR Associate’s Degree in Biotechnology, Biology, Life Sciences, or related field GMP or biopharmaceutical manufacturing Aseptic technique / cleanroom work Batch records and SOP-driven environments Cell culture or biologics manufacturing Manufacturing shift work Our client is a leading Healthcare Industry, and we are currently interviewing to fill this and other similar contract positions. By applying to our jobs, you agree to receive calls, AI-generated calls, text messages, or emails from Pyramid Consulting, Inc. and its affiliates, and contracted partners.