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Perform all aspects of processing: preparation of equipment, disassembling equipment, assembling process equipment, perform CIP and SIP of equipment, perform pressure tests of equipment, perform I Testing of filters, calibration and use of analytical equipment.
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Knowledge of biotech manufacturing process and equipment including cell culture, depth and tangential flow filtration, column chromatography, protein purification and formulation and/or buffer and media operations.
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Perform all aspects of processing: preparation of equipment, disassembling equipment, assembling process equipment, performing CIP and SIP of equipment, performing pressure tests of equipment, performing I Testing of filters, calibration and use of analytical equipment.
$28 - $32 an hourExpandApply NowActive JobUpdated 23 days ago - UpvoteDownvoteShare Job
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Proficiency in statistical analysis and experimental design, knowledge of laboratory and pharmaceutical production equipment including bioreactors, chromatography processes, ultrafiltration, diafiltration, sterile filtration, process tanks, and CIP/SIP systems.
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Perform all processing aspects, including preparation of equipment, disassembling equipment, assembling process equipment, performing CIP and SIP of equipment, performing pressure tests of equipment, performing I Testing of filters, calibration, and using analytical equipment.
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Operate large scale bioprocess equipment for the Cell Culture and Purification operations. Schedule Notes Positions may be 5 x 8 hour shift, 4 x 10 hour shift, 3 x 12 and 4x12 hour shift. These engineers, technicians, scientists and support staff build and maintain BioMarin's cutting-edge manufacturing processes and sites, provide quality assurance and quality control to ensure we meet regulatory standards, and procure the needed goods and services to support manufacturing and coordinating the worldwide movement of our drugs to patients.
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Broad experience in all process areas across multiple operational scales (Upstream cell culture, downstream processing, buffer and media preparation) and ancillary processes (CIP, SIP). The successful candidate will have strong technical, scientific, management and leadership skills, experience in process development through commercialization of biologics, process technology transfer, project management and the ability to influence across functions.
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Able so CIP/SIP processing equipment. CIP Reclaim tanks and wash outside of tank if needed. Must have knowledge of CIP and cleaning processes and procedures. Communicate with Blender Batcher Operators of previous shifts, regarding current activities in progress before resuming the missing procedures.
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Hands on experience with following systems: interpreting P&IDs, Process Flow Diagrams, Piping and instrumentation Diagrams, equipment/system layouts, CIP skids, SIP systems, WIP skids, CIP/COP of manufacturing vessels and manual cleaning is required.
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Performs COP, CIP, and SIP operations to prepare equipment for manufacturing operations. The Manufacturing Technician I learns and performs a variety of tasks with supervision and in accordance with the manufacturing instruction set inclusive of current GMP/ISO requirement and standards and following all safety guidelines of PCI. With supervision, the technician performs routine and critical manufacturing operations, including but not limited to work functions in equipment prep, formulation, aseptic compounding, and filling activities for biopharma and medical device products.
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Clean in Place (CIP) and Steam in Place (SIP) of fixed tanks/vessels and portable equipment and Clean out of Place (COP)/Glass wash of misc. Operation and practical knowledge of CIP, SIP, glass washers, autoclaves, filters, pumps and analytical equipment to support and monitor the process is expected.
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Experience working with fermenters/bioreactors, holding tanks, aseptic operations, seed scale-up, CIP and SIP of process equipment is preferred. The Manufacturing Associate II, Upstream Processing works in a hands-on capacity in the cGMP fermentation and production support areas to manufacture collagenase clostridium histolyticum bulk drug substance (CCH BDS.
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Perform equipment cleaning and sterilization, manual cleaning, clean in place (CIP), steam in place (SIP) and pressure tests (PT) How to apply your experience in bioprocess & cell culture to the production of next-generation seafood utilizing cGMP practices.
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Gain qualification to perform CIP, SIP autoclave, small parts preparation. Gain qualification to perform CIP, SIP autoclave, small parts preparation. Required to work an alternate work schedule (10-hour shift / 4 days a week) including a weekend day and possibly holidays.
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Duties include operation, maintenance, cleaning (CIP) and sterilization (SIP) of large scale cell culture bioreactors and associated operations such as media preparation, infection and harvest.
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