Author Jobs in Quincy (MA)
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Search Results - Author Jobs in Quincy (MA)
QinetiQ-Quincy (MA)
material and author fabrication deviations for suppliers
• Support both Devens and Franklin facilities; assist with DoD security clearance if required
Key requirements
• 10-20 years in mechanical design
• Direct project engineering or technical lead...
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Moderna Therapeutics-Quincy (MA)
for method qualification, validation, and transfer
• Maintain continuity of supply for Moderna-specific materials across laboratories
• Collaborate with QC labs, SMEs, and stakeholders to obtain data and finalize GMP documentation
• Author, revise, and review...
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Barry-Wehmiller-Quincy (MA)
Overview
In this role you will serve as a Validation SME, ensuring equipment, utilities, and computerized systems stay in a validated state under regulatory requirements. You’ll lead validation activities, author protocols and reports, and guide...
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Anduril Industries-Quincy (MA)
with documentation of hazards and controls
• Review work instructions and training materials; author Job Hazard Analyses (JHA) and embed required controls, PPE, and safe-work steps
• Engineer and review production equipment safety improvements (lift fixtures...
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Merck Sharp & Dohme (MSD)-Quincy (MA)
aids, and global development procedures
• Mentor junior staff and foster capability development through coaching
• Author clinical documents (protocols, IBs, study reports, regulatory updates) and coordinate WMA/CTD subsections
• Develop study...
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Vertex Pharmaceuticals-Quincy (MA)
and responses as analytical method SME for Biologics
• Author technical documents (SOPs, validation/transfer protocols and reports, risk assessments)
• Coordinate with CMOs/CTOs on work requests, product characterization and technology transfers
• Review method...
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ERM Group-Quincy (MA)
excellence
• Lead desktop studies, field investigations, monitoring, mitigation, and resource management planning
• Mentor mid-level and junior staff
• QA/QC reviews of deliverables by team members
• Primary author or senior reviewer for environmental studies...
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Deloitte-Quincy (MA)
adoption
• Author and review functional specs, user stories, and test scripts for implementations
Key requirements
• 3+ years of IT experience
• 2+ years of Salesforce B2B Commerce Cloud experience
• 1+ years configuring Salesforce B2B Commerce (Lightning...
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Deloitte-Quincy (MA)
Author and review functional specs, user stories, and test scripts
Key requirements
• 7+ years IT experience
• 4+ years Salesforce B2B Commerce Cloud experience
• 3+ years configuring Salesforce B2B Commerce (catalogs, price books, promotions...
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Humana-Quincy (MA)
operations, and insight
• Author and maintain reference architectures for data platform, clinical documents NLP, RPA/automation, and interoperability patterns
• Lead architecture checkpoints and risk reviews to ensure compliance with enterprise guardrails...
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Klaviyo-Quincy (MA)
lead readiness reviews and post-incident learning
• Author ADRs/RFCs; establish data contracts and schema governance; standardize connectors and templates
• Profile and optimize systems for performance and cost; collaborate with FinOps on unit economics...
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ERM Group-Quincy (MA)
level oversight (inventory, survey, testing, data recovery)
• Experience as primary author/ reviewer of agency-reviewed technical reports (Class I/III, NEPA sections, Cultural Resources Treatment Plans)
• Experience interacting with regulatory agencies...
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ERM Group-Quincy (MA)
survey, testing, and/or data recovery
• Experience as primary author on agency-reviewed technical reports
• Strong documentation and attention to detail
• Familiarity with cultural resources permitting regulations (e.g., FERC, USACE, THC)
• Excellent...
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Liberty Mutual-Quincy (MA)
and collaborate to address them.
• Serve as primary author/presenter of AI Backbone updates to Tech ELT, SLT, and business leadership, translating technical progress into executive narratives.
• Identify opportunities to simplify and mature the Backbone operating...
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Ironwood Pharmaceuticals-Quincy (MA)
and coordinate cross-functional activities
• Lead or co-author study synopses, protocols, amendments, and ICFs with cross-functional input
• Manage day-to-day study conduct, timelines, risks, and issue escalation
• Act as protocol expert for internal teams...
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