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 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.
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.
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.
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.
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.
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.
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.
Manager, Accounts Receivable KYOCERA Document Solutions America, Inc.Manager, Accounts ReceivableWilmington, Massachusetts$74,000–$122,000 / yearThe company’s portfolio includes reliable and eco-friendly MFPs and printers, as well as business applications and consultative services which enable customers to optimize and manage their document workflow, reaching new heights of efficiency. The AR Manager leads Accounts Receivable operations for KDS New England, overseeing cash application, customer master data integrity, reconciliations, and compliance with financial controls.
Director, Quality Assurance and Regulatory Affairs Meridian Bioscience IncDirector, Quality Assurance and Regulatory AffairsNorth Billerica, MAEnsure proper and timely preparation and maintenance of national and international new product submissions, registration/licensing renewals, product listings, post market surveillance reports, import and export documents, safety testing, and other national and international requirements. At least 10 years' experience leading in the medical devices industry; experience regarding medical device design, development and manufacturing regulations, specifically21 CFR Part 820 Quality System Regulation, the IVD Directive 98/79 EC, as well as ISO 13485 requirements.
Vice President, Quality Management Systems And Digital Compliance Intellia TherapeuticsVice 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.
Lead Quality Engineer HitachiLead Quality EngineerSouth Boston, MassachusettsIf you are passionate about data-driven decision-making, problem-solving, and developing world-class quality systems, we invite you to help shape the future of sustainable energy with Hitachi Energy. As part of our recruitment process, Hitachi Energy uses digital and automated tools, including Al-supported solutions, to assist with activities such as application screening, job matching, and interview scheduling.
Administrative Assistant Apidel TechnologiesAdministrative AssistantBoston, MAContractorA high school diploma or equivalent from an accredited institution with the ability to comprehend, communicate and respond to instructions, orders, signs, notices, inquiries, etc. in English and 5 years of project administration or coordination duties supporting a large department or group may be substituted for the degree requirement. Available to work as per assignment by the MBTA twenty-four (24) hours per day, seven (7) days per week as directed by supervisory staff for severe weather conditions, emergencies or any other circumstances that may potentially impact service or the safety of service.
Director of Engineering, Energy Storage SOLV Energy LLCDirector of Engineering, Energy StorageMARemote$170,074–$226,199 / yearFoster effective communication and collaboration between the Energy Storage Engineering group and cross-functional teams, including internal and external engineers, business development managers, project managers, pre-construction managers, procurement specialists, schedulers, estimators, and construction teams. In addition, candidate introductions or resumes can only be submitted to our internal talent acquisition recruiting team if a signed vendor agreement is already on file and the third-party recruiter or agency has received formal instructions from our internal talent acquisition team to submit candidates for a particular job posting.
GelSight: Director of Compliance and Quality Anzu PartnersGelSight: Director of Compliance and QualityWaltham, MAFull timeLead investigations into significant quality issues related to product and material including partnering with Product Management for MRB (Material Review Board) reviews and dispositions, identification of root causes, and development of appropriate corrective and preventive actions. Lead a Quality Team and guide the organization to ensure the design, implementation, and continuous improvement of quality system supports effective product development, manufacturing, and fulfilment across the product lifecycle.
GMP Compliance Manager (Devens, MA) The Facilities GroupGMP Compliance Manager (Devens, MA)MACSI International Inc, founded in 1989, provides integrated building services to clients in real estate, property management, pharmaceuticals, telecommunications, higher education, manufacturing, and insurance. This position ensures that cleaning activities, employee training, documentation practices, and quality systems comply with current Good Manufacturing Practices (cGMP), site procedures, and client requirements.
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.
New2nd shift - GMP Operational Quality Sr. Specialist (QA on the floor) (Contract) 649 Vertex Pharmaceuticals2nd shift - GMP Operational Quality Sr. Specialist (QA on the floor) (Contract) 649Boston, Massachusetts$65–$70 / hourFull timeAgreeing to the Atrium Terms and Conditions, includes permission to use the email address and mobile phone number you provide during the application process or throughout the duration of your prospective or actual employment to notify you of job openings, profiles, articles, news, and other employment-related information, as well as to notify you of special promotions or additional products and services offered by us or our affiliates and partners. Job Description: The Quality Shop Floor Specialist is responsible for the floor quality oversight of the production of autologous cell and gene therapy product in a controlled cGMP cleanroom environment.