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Maintain compliance to cGMP/ISO systems. Must be comfortable in working with animal tissue (skin and/or biological fluid) Manufacture biologically derived medical devices in a clean room environment (must be willing and able to follow clean room dress code requirements.
$21 - $23 an hourExpandApply NowActive JobUpdated 2 days ago - UpvoteDownvoteShare Job
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Develop cloud-native solutions to promote integration within the IT framework across various North American commodity markets, including energy, capacity, ancillary services and power & gas basis markets in the major ISO regions (PJM, CAISO, NYISO, MISO, SPP, ISO-NE, ERCOT, IESO, AESO.
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The Electric Utilities Interconnection Engineer will execute all aspects of utility interconnection projects, working closely with utilities such as Eversource, PECO and BGE and Independent System Operators (ISO) ISO-NE and PJM, internal teams, external consultants, and third-party development partners to facilitate the successful integration oflarge-scale industrial heat pumps and electric boilers onto the electric grid.
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This individual will be a contributing team member in our Process Optimization and Robotics Consulting practice, while working alongside the client and their teams on various areas including ISO, SOC, CCPA/CPRA, GDPR, ISMAP. RPA Development and Process Automation for internal audit processes, security and compliance processes, financial processes, business processes, and similar engagements.
$70,000 - $147,767Full-timeExpandApply NowActive JobUpdated Yesterday - UpvoteDownvoteShare Job
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Provide strategic direction related to business growth and work winning in ISO-NE, NYISO, PJM MISO and ERCOT. Lead the business development activities of the Power Systems function with special focus on the selected ISO/RTO.
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Evaluations and calculations for demonstrating compliance with applicable NERC, ISO, and NRC regulations. Evaluations and calculations for demonstrating compliance with applicable NERC, ISO, and NRC regulations.
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Working knowledge of International and EU/NA Standards such as EU Machinery Directive, ISO, IEC, ANSI, NFPA, UL, OHSA, CFR, NFPA, ANSI, FCC. Amazon Robotics’ Environmental Health and Safety Team is seeking a Senior Safety Engineer to support our automation technology development and manufacturing teams.
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Create new manufacturing documentation and updating/enhancing existing documentation which conform to Quality System Regulations (QSR's) ISO Standards. Knowledge of FDA QSR's and ISO regulations is helpful.
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Other Responsibilities include: Writing and updating the support documentation (APs, TPs, and OIs) for the process, developing, writing and performing IQ, OQ and VQs used in the manufacturing of Test Strips.
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This position offers a hybrid work schedule requiring you to be in the office 3 days a week and an option to work from home two days out of the week (unless a specific business need arises requiring in-office attendance on other days).
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Knowledge of ISO, FDA, and QSR concepts and guidelines as well as other national and international regulations and standards. Participate in FDA inspections, ISO Registration and surveillance audits and customer audits.
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And continuous improvements and compliance of Quality Management Systems (QMS) following FDA and ISO regulations. as “Management Representative”, leading all regulatory inspections related to medical device and combination products (FDA/ISO.
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Supports regulatory compliance to QSR, ISO, MDSAP, CE and other worldwide regulatory requirements as appropriate through customer complaints, internal and external audits, and training systems. In this role as a Senior Regulatory Affairs Specialist at Convatec, you will be responsible for leading regulatory strategy and driving registrations across international markets for Convatec's Advanced Wound Care division.
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Experience with medical device development under FDA Quality Systems Regulations, CE Marking, and ISO Quality Systems. haemonetics.com is Haemonetics Corporation, 125 Summer Street, Boston, Massachusetts, 02110 U.S.A. The global Data Privacy Officer of Haemonetics can be reached at this address.
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Working knowledge of FDA, ISO, CLIA and CAP regulations. The Senior Project Manager, Portfolio and Program Management is responsible for the planning and execution of new biopharma clinical product development projects and/or lab expansion projects, as well as other business critical initiatives.
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iso job in Woburn, MA
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