Coordinator, Demand Generation Compass IncCoordinator, Demand GenerationBoston, MA$30–$36 / hourThis role will serve as the operational engine behind Demand Gen, ensuring campaigns are well-organized, accurately launched, properly tracked, and continuously improved across brands, channels, and markets. Comfortable working in tools such as HubSpot, Salesforce, Meta Ads Manager, project management platforms, spreadsheets, dashboards, or similar systems.
["Senior Product Designer (Legal)","Senior Product Designer (Legal)"] Blink["Senior Product Designer (Legal)","Senior Product Designer (Legal)"]Boston$135,000–$140,000 / yearWhat you'll be doing: Lead end-to-end design initiatives for assigned products and features, owning work from discovery through delivery in close partnership with the product manager and product analysts. Drive systems-level design by identifying and developing reusable patterns, components, and tools that enable scalable, high-quality experiences across products and platforms.
Quality Assurance Integrated Resources, IncQuality AssuranceAndover, MassachusettsContractorQualificationsMinimum BS in biology, engineering or related sciences with at least 3 years of pharma/biopharma experience in a QA or validation roleStrong working knowledge of global GMPs with emphasis on validation, including computer validationStrong interpersonal, oral and written skillsAdditional InformationWe do have referral bonus of $500 per candidate, if you refer any of your friends or colleague who are looking out for the same job. Successful candidate requires a strong working knowledge of global GMPs with an emphasis on validation lifecycle including computer system validation, 21 CFR Parts 210 and 211, and Part 11, Electronic Records and Electronic Signatures.
Aerospace QA Engineer (Quality Engineer) Redwire SpaceAerospace QA Engineer (Quality Engineer)Marlborough, Massachusetts$85,000–$110,000 / yearTo conform to U.S. Government space technology export regulations, including the International Traffic in Arms Regulations (ITAR) you must be a U.S. citizen, lawful permanent resident of the U.S., protected individual as defined by 8 U.S.C. 1324b(a)(3), or eligible to obtain the required authorizations from the U.S. Department of State. These cutting-edge capabilities address cost and performance limitations that are helping to revolutionize spaceflight and are currently being utilized on missions with NASA, the Department of Defense, and several commercial space companies.
Sr Director, QA- GxP Systems Candel TherapeuticsSr Director, QA- GxP SystemsNeedham, MA$258,333–$280,000 / yearEnsure audit-ready files and streamlined workflows What You Bring • Bachelor's degree in Life Sciences or a related technical field.• 10+ years of experience in biotech/pharma Quality Assurance, with direct ownership of GxP systems and a proven track record managing audits, vendors, and validations.• Training & Continuous Improvement:Deliver GxP systems training and drive continuous improvement initiatives, trend analysis, and knowledge management across the org.• Documentation & Record Management:Oversee document bundling, review, and archiving for key deliverables like batch records, stability studies, and QA releases.
Quality Assurance Analyst I Global Payments IncQuality Assurance Analyst IMA$87,300–$128,700 / yearAs a Quality Assurance Analyst, you will contribute to delivering high‑quality software by supporting quality engineering and testing activities, collaborating closely with your team, and building strong technical and domain knowledge. 3-5 years of practical experience working in a Quality Assurance or Test Automation role, supporting automated and manual testing activities with Microservices APIs.
Project Inspector/ QA Manager- Travel Required CBRE Group IncProject Inspector/ QA Manager- Travel RequiredBoston, MACollaborate with various internal and external program stakeholders including third party vendors, contractors and other site personnel to successfully coordinate and drive projects to completion. About the Role: As a Project Inspector/ QA Manager, you will be responsible for overseeing and supervising installation and construction activities onsite to ensure successful timely delivery and completion.
QA Compliance Lead Integrated Resources, IncQA Compliance LeadMarlborough, MassachusettsContractorcharts and docs or temp related excursions - Review and update label issuance and reconciliation processGeneral QA documentation support to include the following: - Issuance of batch records and issuance and tracking of log books, lab notebooks, and SOP binders - Scanning and filing of excursion docs and client related batch docs to support batch release - Develops process improvement plans using a variety of quality and continuous process improvement tools, including but not limited to Six Sigma, Lean Manufacturing, SS, SPC, engineering studies, DOE Gauge R&R, etc. - Communicates and implements a strategy to ensure compliance - Responsible for review of batch records in support of disposition of bulk drug substance - Responsible for review of equipment validation protocols and report - General compliance quality systems management support for the following areas: - Raw material and solution release - Review of raw material specifications and solution docs - Release of single use disposable product to include label reconciliation - Review of temp.
Software Quality Assurance Engineer, AVP State Street CorpSoftware Quality Assurance Engineer, AVPBurlington, MA$80,000–$140,000 / yearWe are seeking a skilled Software Quality Assurance (SQA) Engineer to support an Enterprise web platform (React-based/HTML/JavaScript) backed by Java micro services used by Charles River clients and internal users for self‑service capabilities. Design, document, and execute functional test cases covering end‑user web workflows, configuration changes, validations, approvals, and backend interactions exposed through the UI.
Quality Assurance Specialist Actalent IncQuality Assurance SpecialistBedford, MA$30–$33 / hourIf you would like to request a reasonable accommodation, such as the modification or adjustment of the job application process or interviewing process due to a disability, please email actalentaccommodation@actalentservices.com for other accommodation options. We help visionary companies advance their engineering and science initiatives through access to specialized experts who drive scale, innovation and speed to market.
QA Automation Engineer Bright Vision TechnologiesQA Automation EngineerBurlington, MARemote$100,000–$150,000 / yearJob Title: QA Automation Engineer Location: 100% Remote (U.S.) Position Type: Full-time, Direct W2 Salary Range: $100,000–$150,000 Annually Experience Required: 6+ years Sponsorship: U.S. Citizens, Green Card Holders, EAD Holders, and H-1B transfer candidates are encouraged to apply. The ideal candidate will combine strong hands-on experience with modern automation frameworks with a clear understanding of testing strategy, including risk-based testing, exploratory testing, and continuous testing in Agile environments.
Quality Assurance Technician Actalent IncQuality Assurance TechnicianBurlington, MA$30–$40 / hourWe are proud to be an Engineering News-Record (ENR) Top 500 Design Firm for our engineering design services and a ClearlyRated Best of Staffing winner for both client and talent service. In this role, you will be responsible for reviewing and verifying Quality Control (QC) data, ensuring documentation accuracy, and supporting batch record and patient record review activities.
Associate Director, GCP/GLP/GVP QA Rhythm Pharmaceuticals IncAssociate Director, GCP/GLP/GVP QABoston, MA$160,000–$240,000 / yearLead or assist with GCP health authority inspections, assist clinical teams in preparation for inspections, and provide GCP compliance technical support during inspections of vendors, clinical investigator sites and Rhythm. Manage Rhythm's QMS for Clinical QA activities, including development and management of controlled documents and training matrices, audits, CAPAs/deviations and management and approval of related documentation.
QA Documentation Associate Integrated Resources, IncQA Documentation AssociateCambridge, MassachusettsContractorInc. 5000 - 2007, 2008, 2009, 2010, 2011, 2012, 2013 & 2014 (8th Year)Certified MBE I GSA - Schedule 66 I GSA - Schedule 621I I GSA - Schedule 70(W) 732-429-1913| (F) 732-549-5549 QualificationsRequired Experience:• Incumbent should have a Bachelor of Science Degree or Bachelors in Library Science or 3 years related industry experience.• Prior experience in pharmaceutical, biotech manufacturing or library science environment is preferred.•
Senior Data Quality Assurance Analyst LancesoftSenior Data Quality Assurance AnalystQuincy, MA$60This includes creating a consolidated Enterprise Data Platform on modern cloud tools (including AWS & Snowflake,) and re-platforming existing business data applications from solutions such as SAS and legacy databases to the new platform. This position works collaboratively with epidemiologists, program staff, analytics teams, developers, and external partners to maintain data integrity across state public health information systems and reporting processes.
Software Quality Assurance Engineer II/III Textron IncSoftware Quality Assurance Engineer II/IIIWilmington, MA$92,600–$176,200 / yearRecruiting Company: Textron Systems Primary Location: US-Massachusetts-Wilmington Job Function: Engineering Schedule: Full-time Job Level: Individual Contributor Job Type: Experienced Shift: First Shift Travel: Yes, 10 % of the Time Relocation: Unavailable Job Posting: 05/12/2026, 4:35:16 PM Job Number: 341851. Benefits may include health insurance and prescription plan coverage, dental insurance, family building benefits, vision insurance, mental health resources, flexible spending accounts, health savings accounts, retirement savings plans, life and disability insurance programs, and programs that provide employees time away from work.
Quality Assurance, Officer State Street CorpQuality Assurance, OfficerBurlington, MA$70,000–$118,750 / yearProvide testing leadership by identifying opportunities for improvement in the Scrum team's QA methodology, innovate by researching and recommending new approaches to automation of testing, including use of Artificial Intelligence. Our vision is to be the world's leading investment platform, shaping the future of the industry and driving new levels of technology-led innovation, resiliency, efficiency and growth for investors and the people they serve.
Senior Design Quality Assurance Engineer Beaver-Visitec International IncSenior Design Quality Assurance EngineerWaltham, MAAs one of the fastest-growing, diversified surgical ophthalmic businesses in the world, our purpose-built portfolio of trusted brands includes: Beaver (Knives and Blades), Visitec (Cannulas), Malosa (Single-Use Instruments), Vitreq (Vitreoretinal Surgical Products) and PhysIOL (Premium IOLs), and spans more than 90 countries. We've set our sights on touching the lives of millions of patients affected by conditions such as cataracts, refractive error, glaucoma, retinal disease, and dry eye.
Contract Quality Assurance Inspector Redwire CorpContract Quality Assurance InspectorMarlborough, MA$26–$35 / hourThese cutting-edge capabilities address cost and performance limitations that are helping to revolutionize spaceflight and are currently being utilized on missions with NASA, the Department of Defense, and several commercial space companies. To conform to U.S. Government space technology export regulations, including the International Traffic in Arms Regulations (ITAR) you must be a U.S. citizen, lawful permanent resident of the U.S., protected individual as defined by 8 U.S.C. 1324b(a)(3), or eligible to obtain the required authorizations from the U.S. Department of State.
QA/QC Specialist III Integrated Resources, IncQA/QC Specialist IIILexington, MassachusettsContractorProvide QA guidance/review/approval for Product Development projects in Phase 1 to Phase 3.• Oversee appropriate Quality Systems appropriate for Clinical Phase Materials.• QA Contact for applicable Quality Systems related to R&D.• Review and approved: Master Batch Records, executed batch records, deviations, CAPA and change controls.• Responsibilities• Support of Clinical Operations including Drug Substance, Bulk Drug Product Manufacture, Clinical Packaging & Labeling and oversight of Clinical CMOs and Distributers• Reviewing QC data and COA approval.•