Senior Director, Pharmacovigilance (PV) Sciences Keros TherapeuticsSenior Director, Pharmacovigilance (PV) SciencesLexington, MA$245,000–$302,000 / yearLead and manage all medical safety and risk management related projects including planning, tracking and execution; provide vendor oversight for quality of ICSRs, similar case analysis, and aggregate safety reporting; lead initiatives from the scientific and PV regulation perspective such as inspection readiness, and launch readiness. The Senior Director, PV Sciences is responsible for safety surveillance and aggregate safety reports and works with PV physicians for signal/risk management for Keros products to support product safety and compliance with global drug safety regulations and functional procedures and provide vendor oversight to PV vendors.
Direct Sales Account Executive Transaction Network Services IncDirect Sales Account ExecutiveMassachusetts, MARemote$149,000–$181,000 / yearThe Direct Sales AE owns and develops the customer relationships, addressing needs and issues through a thorough understanding of the customers' business, and then works with the internal product and engineering teams to define operator technical requirements to define solutions. The right candidate will possess strong communication skills and a proven track record of initiative and success positioning, managing and deploying network and client products into North American operators.
NewScientist- #26-18551 US Tech Solutions, Inc.Scientist- #26-18551Lexington, MAThe role is intended to provide dedicated technical and operational capacity across mid-stage and late-stage development programs, ensuring studies are executed on schedule, manufacturing activities are appropriately supported, and program documentation is complete and accurate. Test in-use study samples using relevant physicochemical and analytical methods, including micro-flow imaging (MFI) for subvisible particles, pH, osmolality, protein concentration, and size-exclusion chromatography (SEC); generate, review, and trend the resulting data.
VP, Marketing BusRightVP, MarketingBoston, MAReporting directly to our CEO and working closely with teams across the Commercial organization, the VP of Marketing will be responsible for developing and executing a strategy that generates demand, improves conversion, and delivers messaging, campaigns, and programs that move prospects through the sales funnel. That’s why we built BusRight, a modern transportation platform trusted by hundreds of thousands of Transportation Directors, drivers, and parents across the country to make school transportation safer, smarter, and more equitable.
Associate Director, PV Scientist Biogen IdecAssociate Director, PV ScientistCambridge, MA$172,000–$237,000 / yearRegular employees are eligible to receive both short term and long-term incentives, including cash bonus and equity incentive opportunities, designed to reward recent achievements and recognize your future potential based on individual, business unit and company performance. Oversee signal detection and management activities, Risk Management Plans (RMPs - core and EU), and aggregate reports such as Development Safety Update Reports (DSURs), Periodic Benefit Risk Evaluation Reports (PBRERs).
Assistant / Associate Scientist - Msat Materials & Cryogenics SOKOL GxP ServicesAssistant / Associate Scientist - Msat Materials & CryogenicsDevens, MA$35.90–$41.90 / hourThis role will focus on cryogenics, cold-chain transportation, single-use systems, materials-related technical evaluations, and lab-based studies supporting commercial biopharmaceutical manufacturing operations. Minimum Bachelor’s degree with 2+ years of industry experience, or Master’s degree in Chemical Engineering, Biochemical Engineering, Chemistry, Biochemistry, Biology, or a related scientific discipline.
Automotive Service Writer Midway Automotive CorpAutomotive Service WriterAbington, MAFull timeMidway Automotive Corp is looking for a motivated and customer-focused Automotive Service Writer to join our team in Abington, MA! This is your opportunity to be the vital link between our valued customers and our skilled technicians, ensuring every vehicle gets the care it deserves.
Technical Writer Hudson ManpowerTechnical WriterBoston, MassachusettsThe ideal candidate will work closely with infrastructure, application, and business teams to produce clear, accurate, and user-friendly documentation while working onsite at the client's US office. We are seeking a Technical Writer to support an Investment Banking client by creating, maintaining, and updating technical and operational documentation.
Grants writer UPPERKUTS BOXING CLUBGrants writerASHLAND, MARemoteFull timeAs our Grants Manager, you will be responsible for overseeing current and future programs and endeavors that are currently funded by grants, performing any and all pre- and post-award requirements and functions for grants, and managing financial projections for these programs. You will also work closely with other departments to determine their financial needs, work with grant writers to determine the best grants to apply for, and conduct annual or spontaneous audits as needed.
Principal Engineer, AI Authoring Vertex PharmaceuticalsPrincipal Engineer, AI AuthoringBoston, Massachusetts$166,640–$250,000 / yearYou will tackle complex engineering challenges, including automated document workflows and Retrieval-Augmented Generation (RAG)-based architectures, to support the creation of high-quality, compliant, and efficient regulatory documents. At Vertex, our Total Rewards offerings also include inclusive market-leading benefits to meet our employees wherever they are in their career, financial, family and wellbeing journey while providing flexibility and resources to support their growth and aspirations.
Senior Science Editor and Awards Coordinator Brigham and Women's HospitalSenior Science Editor and Awards CoordinatorBoston, MA$79,560–$115,720.80 / yearPOSITION SUMMARY: Reporting to the Associate Director of Ophthalmology Communication at Harvard Ophthalmology, the Senior Communications Specialist oversees a diverse portfolio of internal and external communications across the Mass General Brigham and Harvard Departments of Ophthalmology, develops original written content for departmental communications and media, serves as the primary scientific contributor and editor of departmental publications, provides direct support to the Chair of Ophthalmology, and oversees the Harvard Ophthalmology nominations processes for internal and external awards. Primary departmental expert resource expert resource and high-level strategic advisor for nominees throughout the application process-providing guidance on award-specific requirements and questions, advising on nomination framing, and leveraging institutional knowledge to identify and recommend the strongest possible letter writers; responsibilities include: Communicating award requirements with the nominee and defining timelines for required materials.
Senior Science Awards Coordinator Brigham and Women's HospitalSenior Science Awards CoordinatorBoston, MA$79,560–$115,720.80 / yearPOSITION SUMMARY: Reporting to the Associate Director of Ophthalmology Communication at Harvard Ophthalmology, the Senior Communications Specialist oversees a diverse portfolio of internal and external communications across the Mass General Brigham and Harvard Departments of Ophthalmology, develops original written content for departmental communications and media, serves as the primary scientific contributor and editor of departmental publications, provides direct support to the Chair of Ophthalmology, and oversees the Harvard Ophthalmology nominations processes for internal and external awards. Primary departmental expert resource expert resource and high-level strategic advisor for nominees throughout the application process-providing guidance on award-specific requirements and questions, advising on nomination framing, and leveraging institutional knowledge to identify and recommend the strongest possible letter writers; responsibilities include: Communicating award requirements with the nominee and defining timelines for required materials.
SOP Writer III Integrated Resources, IncSOP Writer IIICambridge, MassachusettsContractorThis includes but is not limited to: review of regulatory requirements, quality facilitation of procedural document work groups, authoring, reviewing, editing and quality control of documents, identification and assignment of training in the Learning Management system, and training development and implementation. The Consultant SOP Writer must have strong time management and project management skills as well as excellent interpersonal skills and attention to detail to lead content experts through the development of multiple Procedural Documents.
Validation Engineer III Barry-Wehmiller Companies IncValidation Engineer IIIBoston, MABy blending people-centric leadership with disciplined operational strategies and purpose-driven growth, Barry-Wehmiller has become a $3 billion organization with nearly 12,000 team members united by a common belief: to use the power of business to build a better world. The Validation Engineer III will serve as a key member of the validation team, providing expert-level support to ensure facility equipment, utilities, processes, instrumentation, and computerized systems are qualified and maintained in a validated state in compliance with applicable regulatory requirements.
Technical Content Developer, Cloud Accenture PlcTechnical Content Developer, CloudBoston, MADevelop technical learning experiences (courses, modules, hands-on labs, projects, quizzes, and assessments) against defined design requirements and learning objectives for the cloud domain. As a Technical Content Developer, you'll take design requirements and learning objectives from the pod roadmap and partner with subject matter experts to build course modules, hands-on labs, projects, and assessments.
Sr Scientist, Analytical Sciences bluebird bio, Inc.Sr Scientist, Analytical SciencesSomerville, MA$127,000–$164,000 / yearThe ideal candidate will bring deep hands-on expertise in cell and gene therapy (CGT) analytical development, a proven track record of successful assay troubleshooting and tech transfers, and the scientific rigor required to bridge the gap between early scientific assay development and commercial QC operations. This individual contributor role will be responsible for designing and executing internal analytical testing for process development, innovating and qualifying new analytical assays, and leading the end-to-end technical transfer of these methods to external QC laboratories.
New["Merchandising Coordinator","Merchandising Coordinator"] Venturefizz Product Management Community["Merchandising Coordinator","Merchandising Coordinator"]Cambridge$48,000–$50,000 / yearResponsibilities Could Include: Write, edit, and proofread enticing, error-free copy for books and other book marketing content, matching Chirp's brand voice and encouraging readers to click and buy. This new team member will help to support the team with editing, curating, and merchandising content for our large community of audiobook lovers across email and on the Chirp website.
Customer Enablement Lead (US) Realtime RoboticsCustomer Enablement Lead (US)Boston, MassachusettsThis role owns the self-service layer of the customer experience: the documentation, curriculum, in-product guidance, and content infrastructure that enables customers to resolve issues and build competence without requiring internal support. Build and maintain the content infrastructure: information architecture, authoring and review workflow, versioning aligned to releases, and publishing surfaces (docs portal, in-product help, video, structured courses).
Senior Director, Bioanalytical And Biomarker Development Editas Medicine, Inc.Senior Director, Bioanalytical And Biomarker DevelopmentCambridge, MA$270,000–$300,000 / yearThis highly visible role will be accountable for the preclinical bioanalytical strategy, biomarker strategy, data quality, and regulatory readiness, ensuring successful EDIT-401 IND submission and Clinical Trial execution. Characterizing Your Impact: As the Senior Director, Bioanalytical and Biomarker Development, you will: Lead assay development, qualification, validation, and execution for measuring drug product components, immunogenicity, biomarkers, and other analytes in biological matrices.
Senior Scientist, Analytical Development CRISPR TherapeuticsSenior Scientist, Analytical DevelopmentSouth Boston, MassachusettsThe Company has evolved from a pioneering research-stage organization into an industry leader, marking a historic milestone with the approval of CASGEVY® (exagamglogene autotemcel [exa-cel]), the world’s first CRISPR-based therapy, approved for eligible patients with sickle cell disease and transfusion-dependent beta thalassemia. Lead a team responsible for the development, optimization, and technology transfer and qualification of cell-based assays for Drug Products and Drug Substances across the CRISPR portfolio, including potency assays for ex-vivo and in-vivo programs.