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Manage a team of Manufacturing Associates in Protein Purification conducting purification operations including chromatography, filtration, titration, and column packing and unpacking. The Manager/Sr. Manager, Protein Purification Manufacturing is responsible for leading, planning and driving the execution of manufacturing production operations in the Protein Purification area of cGMP manufacturing.
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Serve as bioprocess SME that provides technical oversight in support of IND filling and to ensure that clinical manufacturing is successfully executed per schedule. Independently author technical reports of studies, protocols, SOP and risk assessments to enable technology transfer, manufacturing and IND activities.
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Qualifications of the Manufacturing Associate II:·1+ years of experience working in a manufacturing environment for a biopharmaceutical organization (upstream, downstream or fill/finish) ·Bachelor's Degree with 1+ year of experience or Associate's Degree with 2+ years of relevant experienceCompensation of the Manufacturing Technician:·BSalary: Between $55,000 - $70,000 based on years of relevant experience·Full Medical, Dental & Vision Insurance (through Cigna), 401k.
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An established cell therapy biopharmaceutical company is growing their Upstream manufacturing team. Recent experience performing upstream manufacturing activities. 1+ years of Biotech Manufacturing experience.
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Working knowledge of principles and applications associated with manufacturing operations including SPC, Six Sigma, 5S, SMED and Lean Manufacturing. Evaluate manufacturing processes by designing and conducting research, applying knowledge of product design, fabrication, assembly, tooling, and materials.
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Serves on team projects (i.e. qualifications, investigation) in the role of testing support and initiation of investigationResponsible for completing laboratory housekeeping to ensure safety and complianceIdentifies areas for improvement or gaps in both safety and compliance (ZAPs/ZIPs)Effectively communicates issues/hurdles to supervisor and/or managerSupports GSK site initiatives and departmental goalsJob requires gowning into GMP manufacturing spaces to collect samples.
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Previous experience in general labor, loading, unloading, landscaping, construction, production, manufacturing, assembly, or warehouse work is helpful but not required. Provide friendly, positive, and stress-free junk removal to all customers.
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Crown Food North America is searching for a Manufacturing Engineer to join our team to support operations for the Food Division. In addition, this position requires maintaining quality and safety standards, document control, and supporting the engineering needs of the manufacturing facilities.
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Experience with Microsoft D365 (or similar manufacturing ERP environment) preferred. Partner with Finance leadership, IT and business owners to assess all Finance processes (transactional, financial close, financial planning, manufacturing, reporting, etc.
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Qualified candidates will have experience working in labs and clean rooms on computerized scientific or biopharma manufacturing equipment. Serves as technical subject matter expert in support of validated laboratory and manufacturing equipment.
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Develop algorithms and software to provide efficient manufacturing, calibration, and factory testing of active phased-array antennas and satellite user terminals. Assist in troubleshooting of issues in development, manufacturing, and operational environments.
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Familiarity with additive manufacturing technologies like 3D printing. It will be followed by fabricating prototypes, testing them, receiving feedbacks from the end users, and improving the design using additive and subtractive manufacturing techniques.
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Black & Veatch’s Technology, Commercial & Industrial is a specialized group of capabilities focused on the latest needs for clients in a fast-growth technology-led arena of advanced manufacturing, and generative AI computing including gigafactories, bio/ag tech, data centers and distributed infrastructure.
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Implementing Good Manufacturing Practices (GMP) and Good Laboratory Practices (GLP) and data integrity. Designing project and developing technical components of proposals for donor funded programs such as GFATM, Gates Foundation, UNITAID, or WHO.
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Summary of the Role: The Cleaning Specialist is responsible for the daily supervision and training of cleaning personnel in their performance of facility cleaning activities in accordance with Current Good Manufacturing Practices (cGMP’s.
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manufacturing job Company: Ey in Olney, MD
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