Full-Time jobs in the Biotechnology & Pharmaceuticals industry in Peabody, Massachusetts

. The Woburn Biosurgery Manufacturing organization consists of the following product lines: LeGoo and Backstop Manufacturing. This description governs both products. The primary responsibility of the Manufacturing organization is the faithful execution of the current set of instructions, ensuring practice matches procedure, to assure high product quality and compliance with current cGMPs and Genzy...
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Job Summary: The Controlling Sr. Manager is responsible for leading the day to day activities of the U.S. Genzyme CSO (Clinical Sciences and Operations) Financial Controlling function. This position is primarily responsible for ensuring the accurate recording of financial information with respect to Genzyme CSO cost centers, ongoing CSO client support and ensuring adherence to all related financia...
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. Regulatory Affairs, Associate Principal - Site CMC The ideal candidate will have the mix of personal and professional characteristics with emphasis on the following job responsibilities: Provide regulatory support for manufacturing operations at the Allston Landing Biologics Facility. Review technical documentation (Project Plans, Change Control, Deviations, CAPA, Batch Records) Recommends/appro...
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. Regulatory Affairs, Associate Principal - Site CMC The ideal candidate will have the mix of personal and professional characteristics with emphasis on the following job responsibilities: Provide regulatory support for manufacturing operations at the Allston Landing Biologics Facility. Review technical documentation (Project Plans, Change Control, Deviations, CAPA, Batch Records) Recommends/appro...
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. The Allston Manufacturing organization consists of the following functional groups: Upstream Operations, Downstream Operations, Scheduling, and the Warehouse. The primary responsibility of the Manufacturing organization is the faithful execution of the current set of instructions, ensuring practice matches procedure, to assure high product quality and compliance with current cGMPs and Genzyme Qu...
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. * DAYS & HOURS for this position are Fri-Mon : 06:00AM - 4:30PM and 10:00AM - 8:30PM (Every other week rotation) * Quality Assurance (QA) Bulk Operations is responsible for quality oversight of operations at Genzyme's Allston Landing, a large-scale therapeutic protein manufacturing facility. QA Bulk's main function is to ensure CGMPs are being adhered to during manufacturing operations. In suppo...
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. Manufacturing Supervisor, Protein Purification, Nights Hours: 7.00PM to 7.00AM, rotating shift Downstream Operations is responsible for Cerezyme protein purification operations at Genzyme's Allston Landing, a large-scale therapeutic protein manufacturing facility. Downstream Operations' main function is multi-stage large scale chromatography operations. In support of our main functions, our addi...
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. Quality Control Chemistry is responsible for testing intermediate and final product samples to demonstrate that all products meet all standards required for CGMP operations. Various techniques are utilized in Quality Control including, HPLC, GC, Gel Electrophoresis and multiple types of spectrophotometry. Additional functions include raw material testing, stability testing, assay transfers and t...
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. The Quality Assurance Department is accountable for decisions regarding the development, implementation and administration of quality assurance, which must take into consideration the requirements and processes in major functional areas, customer requirements, and numerous intangible variables. The Quality Assurance Department is primarily responsible for oversight over lot release and managemen...
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. The Quality Systems department manages Change Control, Document Control, CAPA, Product Quality Reviews, Quality Engineering, Quality Information Systems and Continuous Improvement activities. The Principle Business Systems Analyst (BSA) will be part of the Allston Biologics Quality Systems group, supporting the site via the administration of the applications that support Quality. This position i...
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. Quality Control Chemistry is responsible for testing intermediate and final product samples to demonstrate that all products meet all standards required for CGMP operations. Various techniques are utilized in Quality Control including, HPLC, GC, Gel Electrophoresis and multiple types of spectrophotometry. Additional functions include raw material testing, stability testing, assay transfers and t...
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. Quality Control Chemistry is responsible for testing intermediate and final product samples to demonstrate that all products meet all standards required for CGMP operations. Various techniques are utilized in Quality Control including, HPLC, GC, Gel Electrophoresis and multiple types of spectrophotometry. Additional functions include raw material testing, stability testing, assay transfers and t...
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. Quality Control Investigator, Chemistry Quality Control Chemistry is responsible for testing intermediate and final product samples to demonstrate that all products meet all standards required for cGMP operations. Various techniques are utilized in Quality Control including HPLC, GC, Gel Electrophoresis and multiple types of spectrophotometry. Additional functions include raw material testing, s...
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. Quality Assurance (QA) Bulk Operations is responsible for quality oversight of operations at Genzyme's Allston Landing Facility, a large-scale therapeutic protein manufacturing facility. QA Bulk's main function is to ensure CGMPs are being adhered to during manufacturing operations. In support of our main function, our additional functions include, issuing production records, log review, review ...
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