Find your next 2nd Shift Pharmaceutical Manufacturing Associate job in Swiftwater, PA. Excellence in Operations Award 2009-Cleaning Characterization Projects, Excellence in Operations Award 2012-Extraneous Matter Project. Operations include CIP, SIP, operation of autoclaves and parts washer, production activities and cleaning of the facility. If interested please reply with resume. Overview: Responsible for manufacture of Master and Working Cell Banks and performing activities within production facilities to support manufacture of Cell & Gene Therapy products, and final product fills according to current Good Manufacturing Practices (cGMPs). Updated on 2020-07-07. Looking for Manufacturing Associate - Biotech jobs at Aerotek. Extensive experience in manufacturing, particularly all aspects of cell culture through purification. electronics assembly, mechanical assembly, modeling) or other equivalent experience, Responsible, as SME, for the training and coaching of other operators and staff on the area for which you are SME, Demonstrated understanding and use of RFT techniques and lean manufacturing concepts, Strong ability to lead, challenge and positively influence in an interactive team environment, Strong computer skills â knowledge of CMMS, Electronic Batch Records, ERP, QMTS, etc, Be a results oriented person with excellent organizational, communicational and team development skills with an ability to successfully interact with people, create a team environment and generate co-operation, Demonstrated ability to deliver to team, site and personal objectives, Ability to assemble, disassemble, operate and understand equipment per procedures, Practitioner level in problem solving skills, Ability to interact constructively with peers, Ability to understand, apply, and evaluate the basic principles of Biotechnology, Tooling preparation and release application, 0-2 Yrs. https://www.velvetjobs.com/resume/associate-manufacturing-resume-sample Please provide a type of job or location to search! All training will be conducted with an emphasis on safety and completion of operations in a timely manner, Report any issues related to manufacturing performance, process and safety to the manager in order to ensure safety, compliance with regulations and cGMPs and to facilitate continuous process improvement, Requires strong problem-solving and troubleshooting skills as demonstrated by a consistent track record of solutions to technical problems within large scale cGMP Cell Culture Manufacturing, Independently have the ability to regularly lift, dispense, push and/or pull items up to 50 pounds, Learn and support business systems (Track wise, GCDL, etc. Mention a few hard and soft skills along with personality traits that assist you in your work. All rights reserved. experience with close-tolerance assembly work (e.g. ... • Technical understanding of a biotech manufacturing facility. experience in a composites/manufacturing environment (space/satellite structures, aerospace manufacturing environment preferred) and/or specialized education included in or post HS such as an applicable certification or AA degree, Ability to work Overtime and Weekends as needed, History of dependable supply of safe and effective therapies, Create and maintain accurate daily, weekly, and monthly production schedules, Ensure current schedule is maintained, accurate, and up to date, Maintain excellent lines of communication with production and support staff, Provide emergency scheduling solutions and scenarios due to production/facility related issues, Proactive communication regarding scheduling errors and issues â provide realistic solutions, Represent Finite Scheduling in cross-functional teams and projects when required, Track, analyze and report scheduling metrics on schedule adherence, task adherence, and root cause analysis as required, Assist, plan and implement continuous improvement solutions related to Finite Scheduling, Configure, maintain, and test Electronic Batch Records, Asses and own change controls as they relate to the above systems, Implement activities required in support of global system continuity, Assist in implementing continuous improvement solutions related to PAS|X, Conduct training and share knowledge with other members of the team, Manufacture clinical grade cellular therapeutic products to supply CCT Clinical Program, B.S. 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