Specialist, Quality Assurance Moderna IncSpecialist, Quality AssuranceNorwood, MA$89,900–$143,800 / yearHere's What You'll Bring to the Table: Minimum requirements: Requires a Master's degree, or foreign equivalent, in Engineering Management, Engineering (any), Biology, Chemistry, or related field and 3 years of experience as a Quality Assurance Associate, QA Testing Engineer, Supervising Engineer, Graduate Apprentice, or related position. Must have 3 years of experience with the following: Writing and ensuring compliance to SOPs; Documenting processes, deviations, and corrective actions to maintain quality records; Root Cause Analysis; Technical writing; and.
Principal Program Manager Waters CorporationPrincipal Program ManagerMilford, MassachusettsThe role serves as the primary business-facing lead for PLM delivery, working closely with stakeholders, IT teams, implementation partners, and senior leaders to ensure PLM capabilities support business priorities, regulatory expectations, operational efficiency, and product data governance. Key Words: #Principal Program Manager #Product Lifecycle Management #PLM #Program Leadership #Program Management #Business Transformation #PLM Delivery #Business-Facing Lead #Continuous Improvement #Value Realization
Coordinator III Apidel TechnologiesCoordinator IIICumberland, RIContractorGiven the volume of physical documentation and the timesensitive nature of property tax mattersincluding appeals, statutory notices, and paymentrelated correspondencethis role requires a consistent onsite presence to maintain operational efficiency, document control integrity, and compliance readiness. Prior property tax experience is preferred, along with strong communication skills, sound judgment, and the ability to effectively coordinate with internal teams, vendors, business stakeholders, and landlords while managing multiple priorities with accuracy and accountability.
Absence Management Specialist (Hybrid) Boston Medical CenterAbsence Management Specialist (Hybrid)Boston, MA$21.39–$30.05 / hourWorks with the employee's leave team to ensure proper management of all administrative aspects of leave claims to include: tracking hours used/taken; return to work data; file reviews and working closely with the Managers, HR and Payroll to ensure that key dates, details and status for employee's are accurate and correct. Develops strong working relationships with various internal and external partners including the medical community, Occupational Health, EAP, payroll, legal and others to ensure accurate, efficient, and timely leave administration.
Associate/Sr. Associate - CMC Project Management & Operations Oruka TherapeuticsAssociate/Sr. Associate - CMC Project Management & OperationsWaltham, Massachusetts$104,000–$125,000 / yearOruka’s mission is to offer patients suffering from chronic skin diseases like plaque psoriasis the greatest possible freedom from their condition by achieving high rates of complete disease clearance with dosing as infrequently as once or twice per year. Maintain integrated CMC trackers and timelines for deliverables such as batch records, protocols, reports, specifications, comparability documentation, stability updates, regulatory content, and manufacturing readiness milestones.
Senior Vice President, Project & Program Management WSP Global IncSenior Vice President, Project & Program ManagementBoston, MA$310,000–$325,000 / yearServe as program management discipline subject matter expert to a variety of internal / external entities including Federal, State, and Local Agencies, Clients, Subcontractors, industry-related groups, and various government and community entities. Lead a multi-disciplinary team of engineers and architects for the preparation of final design documents for bored water tunnels with pressure lining, access shafts, valve chambers, near surface structures, and tie-ins to the existing water supply network.
Associate Director, Quality Management Systems Dyne Therapeutics IncAssociate Director, Quality Management SystemsWaltham, MA$160,000–$195,000 / yearRole Summary: The Associate Director, Quality Management Systems is a key member of the quality team responsible for designing, scaling, and advancing a global Quality Management System (QMS) that supports Dyne's transition to commercial operations. The Associate Director partners cross-functionally to embed quality as a strategic enabler of business performance, ensuring systems are fit-for-purpose, inspection-ready, scalable, and efficient as the organization grows.
EHS Specialist Integra LifeSciences Holdings CorpEHS SpecialistBraintree, MA$71,300–$97,750 / yearThe EHS Specialist partners with operations, facilities, engineering, and leadership teams to proactively identify hazards, reduce environmental impact, and improve overall workplace safety and compliance performance. Operating within a GMP-regulated environment, the EHS Specialist partners closely with Facilities, Manufacturing, Quality, and Engineering to ensure that safety and environmental controls are effectively integrated into daily operations.
Quality System Analyst HitachiQuality System AnalystSouth Boston, MassachusettsIf you're passionate about continuous improvement, process excellence, and making a measurable impact in a manufacturing environment, this role offers the platform to grow your career while contributing to products and solutions that help power communities around the world. You'll collaborate with teams throughout the organization to support audits, strengthen quality processes, manage critical documentation, and drive corrective actions that enhance business performance.
Associate Director, Quality Management Systems Dyne TherapeuticsAssociate Director, Quality Management SystemsWaltham, MA$160,000–$195,000 / yearThe Associate Director, Quality ManagementSystems is a key member of the quality teamresponsible for designing, scaling, and advancing aglobal Quality Management System (QMS) that supports Dyne’s transition to commercial operations. The Associate Director partners cross-functionally to embed quality as a strategic enabler of business performance, ensuring systems are fit-for-purpose, inspection-ready, scalable, and efficient as the organization grows.
Senior Quality Systems Engineer Access Vascular IncSenior Quality Systems EngineerBillerica, MA$93,000–$160,000 / yearThis role helps oversee our Quality Management System and provides Quality Engineering support across Operations, working closely with a small, hands-on team under AVI''s QMS and FDA QMSR requirements. Proven track record with implementing, evolving, and improving medical device company quality management systems (QMS) compliant to FDA 21 CFR Part 820, ISO 13485:2016, and ISO 14971.
Senior Director, Pharmacovigilance PV Sciences Keros Therapeutics IncSenior 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.
Vice President, Quality Management Systems and Digital Compliance Intellia Therapeutics IncVice President, Quality Management Systems and Digital ComplianceCambridge, MARemote$319,064–$389,968 / yearAs a transformational leader and executive sponsor for quality system modernization, this position drives digital transformation through eQMS implementation, establishes robust governance frameworks, and ensures sustained regulatory compliance and inspection readiness. This executive role anticipates regulatory trends, manages enterprise risk, and positions quality as a competitive differentiator that directly contributes to business value and organizational success in bringing life-changing therapies to patients.
Associate/Sr. Associate - CMC Project Management & Operations Oruka Therapeutics, Inc.Associate/Sr. Associate - CMC Project Management & OperationsWaltham, MA$104,000–$125,000 / yearOruka's mission is to offer patients suffering from chronic skin diseases like plaque psoriasis the greatest possible freedom from their condition by achieving high rates of complete disease clearance with dosing as infrequently as once or twice per year. Maintain integrated CMC trackers and timelines for deliverables such as batch records, protocols, reports, specifications, comparability documentation, stability updates, regulatory content, and manufacturing readiness milestones.
Manufacturing Engineer QuEra Computing IncManufacturing EngineerBoston, MA5+ years of manufacturing engineering experience supporting electro-mechanical and/or opto-mechanical products, preferably at an OEM that deployed either full turn-key, or outsourcing with in-house final assembly and test approach to production. This role is ideal for someone who thrives in fast-paced product development environments, enjoys building scalable manufacturing processes and systems, and has strong experience supporting New Product Introduction (NPI) and contract manufacturing partners.
Director, Product Quality Lead Tetraphase Pharmaceuticals IncDirector, Product Quality LeadWaltham, MAXACDURO (sulbactam for injection; durlobactam for injection) is a new treatment designed specifically to treat hospital-acquired bacterial pneumonia (HABP) and ventilator-associated bacterial pneumonia (VABP) caused by susceptible strains of bacteria called Acinetobacter baumannii-calcoaceticus complex in adults. ZEVTERA (ceftobiprole) is a newly approved advanced-generation cephalosporin antibiotic and the only FDA-approved cephalosporin specifically designed to treat adult patients with Staphylococcus aureus bloodstream infections (bacteremia) including those with right-sided infective endocarditis.
Senior Manager, Software Device Quality Takeda Pharmaceutical Co LtdSenior Manager, Software Device QualityLexington, MA$137,000–$215,270 / yearThe Senior Manager, Software Device Quality is a seasoned quality and technical leader responsible for supporting software medical devices and combination products across the full product lifecycle - from design and development through manufacturing, distribution, and post-market support. The actual base salary offered may depend on a variety of factors, including the qualifications of the individual applicant for the position, years of relevant experience, specific and unique skills, level of education attained, certifications or other professional licenses held, and the location in which the applicant lives and/or from which they will be performing the job.
Post Closing/HMDA Quality Assurance Specialist Dean Co-operative BankPost Closing/HMDA Quality Assurance SpecialistFranklin, MAWorking in conjunction with the VP Loan Servicing Operations Officer in developing an internal quality assurance auditing program and after identifying areas of concern, the Post Closing/HMDA Quality Assurance Specialist will assist in creating a subsequent training program to enhance post-closing and create efficiencies in loan audits, loan funding, post-closing and servicing. Post-Closing: Assist the VP Loan Servicing Operations Officer in developing an internal pre-funding and post-closing Quality Assurance review process identifying adherence to department procedures, bank policies, regulatory compliance and investor guidelines.
Mechanical Project Engineer J.F. White ContractingMechanical Project EngineerBoston, MA$85,000–$130,000 / yearPart timeWhite Contracting Company's Mechanical Division is seeking a driven and detail-oriented Mechanical Project Engineer to support the delivery of complex HVAC and mechanical construction projects throughout Greater Boston. Bachelor's degree in Construction Management, Mechanical Engineering, Civil Engineering, or a related field — OR — 3+ years of hands-on experience in mechanical or HVAC construction.
Associate/Sr. Associate - CMC Project Management & Operations Oruka Therapeutics IncAssociate/Sr. Associate - CMC Project Management & OperationsWaltham, MA$104,000–$125,000 / yearOruka's mission is to offer patients suffering from chronic skin diseases like plaque psoriasis the greatest possible freedom from their condition by achieving high rates of complete disease clearance with dosing as infrequently as once or twice per year. Maintain integrated CMC trackers and timelines for deliverables such as batch records, protocols, reports, specifications, comparability documentation, stability updates, regulatory content, and manufacturing readiness milestones.