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Author and manage Data Security Plans (DSP) for unique system and operating requirements outside established security policies. Experience with Satellite, ACAS, Splunk and McAfee/Trellix ePO Server Understanding of VMWare/vSphere virtual environments including virtual machine provisioning and resource management (disk, CPU, and RAM monitoring.
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The job purpose and scope of the Clinical Research Scientist is to author the scientific documents associated with design, conduct, and reporting of clinical trials in the therapeutic area of Heart Failure, particularly mechanical circulatory support and hemodynamic monitoring.
$145,300 a yearFull-timeExpandApply NowActive JobUpdated Today - UpvoteDownvoteShare Job
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Author post-market surveillance reports. Author and support regulatory filings for market clearance, licensing, registration, and legalization. The Principal Regulatory Specialist is responsible for carrying out Pre-Market and Post-Market regulatory activities in compliance with Digital Factory’s Quality Management System for domestic and various international markets for SaMD products.
Full-timeExpandApply NowActive JobUpdated 20 days ago - UpvoteDownvoteShare Job
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Contribute to or author proposals and can participate on business capture efforts. RF Engineer Hourly: $70 - $88/hour Location: Chelmsford, MA (fully on-site) Shift: 4/10, 1st shift (6am - 4:30pm) Industry: Government/Defense Employment Type: Long-term contract with potential for permanent employment Clearance: Active Secret Qualifications: BS degree in electrical engineering or closely related technical field.
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Author or revise procedures as needed based on non-conformance material investigation or continuous improvement projects (CIP) in accordance with regulatory and corporate requirements. Join us and discover an environment in which you’ll be supported to learn, grow and become your best self.
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Author audit reports and coordinate supporting documentation; manage same in QMS. Bachelor’s degree in a scientific discipline with 10+ years’ experience in the pharmaceutical or biotech industry and GCP Clinical Quality Assurance.
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As a Quality Assurance Specialist, you will engage in batch record review, assist in writing SOPs, and author Annual Product Review Reports. As a Quality Assurance Specialist, you will engage in batch record review, assist in writing SOPs, and author Annual Product Review Reports.
Full-timeExpandApply NowActive JobUpdated 4 days ago - UpvoteDownvoteShare Job
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Revise and author standard operating procedures/batch records/work instructions to optimize usability and compliance. Point of contact for new manufacturing employee onboarding and Act as a resource/SME.
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Demonstrated leader in the field of geothermal design and construction including presenting at conferences, author, or co-authors of papers. Some of the world’s most pressing problems – from climate change to sustainable development, to critical infrastructure and the future of our energy supply – need our brightest and diverse minds working together to create safer, more resilient communities for tomorrow.
$200,000 a yearFull-timeExpandApply NowActive JobUpdated 12 days ago - UpvoteDownvoteShare Job
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Author and review stability protocols related to the company’s AAV gene therapy and RNA PMO product pipelines. Author and review stability protocols related to the company’s AAV gene therapy and RNA PMO product pipelines.
Full-timeExpandApply NowActive JobUpdated 11 days ago - UpvoteDownvoteShare Job
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Drive projects to improve the QMS for compliance through Trackwise (TW), efficiency, or corporate needs Author/revise standard operating procedures (SOPs) and test methods, as required Other duties as assigned Work Conditions: Office Physical Requirements: Stand, walk, sit, use hands and fingers to handle or feel, reach with hands and arms, stoop, kneel, crouch or crawl, climb or balance Talk or hear Close vision Computer/office machines Lift up to 10 lbs.
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Author high quality and timely investigations within the Pfizer quality systems (i.e. eQMS) Author PQS compliance assessments. Whether you are in the discovery sciences, ensuring drug safety and efficacy or supporting clinical trials, you will apply cutting edge design and process development capabilities to accelerate and bring the best in class medicines to patients around the world.
$107,600 a yearFull-timeExpandApply NowActive JobUpdated 24 days ago - UpvoteDownvoteShare Job
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Build scientific function of safety surveillance and aggregate safety reports, author safety signal assessment reports and aggregate safety reports, write and maintain relevant SOPs and procedures in compliance with global safety regulations and guidelines, and provide training within DSPV and cross-functionally.
Full-timeExpandApply NowActive JobUpdated 20 days ago - UpvoteDownvoteShare Job
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Author, review, and approve SOPs and cGMP documents. 5 years of QA experience in cGMP and FDA inspection. Author, review, and approve SOPs and cGMP documents. Provide QA support for product development.
ExpandApply NowActive JobUpdated 14 days ago - UpvoteDownvoteShare Job
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Author and maintain standard operating procedures (SOPs) and train key personnel as needed. Author and maintain standard operating procedures (SOPs) and train key personnel as needed. The Senior Regulatory Affairs Program Lead is responsible for managing the collaboration with cross-functional stakeholders to ensure regulatory compliance is met.
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author job in Wilmington, MA
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