Arevna is hiring: Manufacturing Associate III (CDMO) in Texas

Biologics CDMO Hiring Opportunity Position: Manufacturing Associate III Location: San Antonio, Texas Overview: We are seeking a talented Manufacturing Associate III to join our team in a biologics-focused Contract Development and Manufacturing Organization (CDMO). This position involves supporting cGMP manufacturing processes in a controlled cleanroom environment. The ideal candidate will have strict attention to detail, a commitment to quality, and the ability to collaborate within cross-functional teams. Key Responsibilities: Execute and document batch records in compliance with current Good Documentation Practices (GDP). Revise and review Standard Operating Procedures (SOPs), batch records, and related documentation. Support upstream/downstream manufacturing processes, including microbial fermentation, mammalian cell culture, and purification techniques. Operate and maintain systems for microbial fermentation, mammalian single-use systems, continuous flow centrifuges, and homogenization. Perform tangential flow filtration (TFF), depth filtration, and chromatography (AKTA, HPLC systems). Conduct drug substance bulk fill, vial fill, and aseptic handling. Collaborate on deviation and CAPA resolution with Subject Matter Experts (SMEs) and quality teams. Support equipment calibration and preventative maintenance. Ensure adherence to safety policies and goals. Education & Experience: Associate’s, Bachelor’s, or Master’s degree in a Scientific or Engineering discipline. 3-4 years of experience in biomanufacturing within a GMP environment. Experience with microbial systems is highly desirable. Strong knowledge of cGMP principles and Quality Management Systems. Knowledge & Skills: Excellent verbal and written communication skills. Strong analytical ability and professional presence. Proficiency in Microsoft Word, Excel, PowerPoint, and Project. Working knowledge of cGMPs and global regulatory requirements. Exceptional interpersonal skills and the ability to lead through influence. High-energy, results-oriented approach to problem-solving and teamwork. Physical Requirements & Working Environment: Flexibility in working hours, including weekends and varying shifts. Ability to gown in cleanroom attire and stand for extended periods. Comfortable working in an environmentally controlled facility. Capability to lift and move up to 20 pounds as needed. This is a great opportunity to contribute to a growing CDMO that prioritizes quality, speed, and flexibility. If you are passionate about biologics manufacturing and thrive in a dynamic environment, we’d love to hear from you How to Apply: Submit your application today to be considered for this exciting opportunity. Qualified candidates will be contacted for further steps.