Manufacturing Associate Downstream (Flex)

Description Looking to join a passionate team dedicated to developing and manufacturing life-saving biopharmaceuticals? Avid Bioservices is a leading clinical and commercial biologics CDMO focused on creating innovative solutions to meet the needs of our clients and improve patient outcomes. Your Role: Join our dynamic team as a  Manufacturing Associate, Downstream ! In this role, you'll be a crucial part of our multi-product manufacturing facility, working in strict compliance with cGMP and Standard Operating Procedures. Your responsibilities will encompass various tasks, including production, meticulous documentation, report writing, materials procurement, and equipment scheduling. You'll be instrumental in ensuring the timely production and release of top-quality products. At our company, we value core principles such as Integrity, Adaptability, Innovation, Teamwork, and Passion, all united by a shared mission to enhance patients' lives through the consistent delivery of high-quality biopharmaceuticals. If you're ready to make a meaningful impact, apply now and be part of our journey! Key Responsibilities: Ensuring the timely setup of equipment and materials for each production run. Planning and preparing all necessary resources for various processes and activities. Operating and diligently maintaining BioProcess chromatography skids. Proficiently handling the packing, unpacking, and cleaning of production-scale chromatography columns. Executing antibody and enzyme purification techniques using Affinity chromatography, Size Exclusion chromatography, Ion Exchange chromatography, Hydrophobic Interaction, and Tangential Flow Filtration (TFF). Conducting pH and conductivity meter calibration and testing. Managing product filtration processes, including sterile filtration, ultrafiltration, and viral filtration. Demonstrating exceptional aseptic techniques with precise, deliberate movements. Participating in product filling, including aseptic processing and media fill qualifications. Upholding the cleanliness and maintenance of cleanroom facilities and equipment. Monitoring and controlling raw material inventory levels. Ensuring compliance with Good Manufacturing Practices (GMP) documentation standards. Taking the initiative to revise and initiate Batch Production Records, Standard Operation Procedures, study protocols, and reports. Leading and managing independent projects as assigned, contributing to the overall success of the manufacturing team. Skillfully preparing media and buffer solutions critical for production processes. Conducting manual cleaning of small parts and equipment to maintain hygiene and efficiency. Performing thorough filter integrity testing using specialized equipment like the Sartocheck 3/4 Filter Integrity Tester. Operating and ensuring the proper maintenance of the ARS Frontier Autoclave. Minimum Qualifications: 2+ years of experience with large-scale liquid chromatography…