NewDirector of Social Services Care-OneDirector of Social ServicesBrookline, MAEnsures and documents that residents/families have input into the care planning process; Acts as liaison between residents, families, outside agencies, and the Center Administrator to ensure that the resident's rights are maintained; Takes responsibility for conducting family meetings as needed; Functions in a management capacity and adheres to all policies and procedures of the Center as a representative of CareOne Administration; Performs administrative requirements such as completing necessary forms and reports under the direction of the Administrator and submitting such reports to the Administrator and/or consultants as required; Facilitates discharge planning including the development of an organized discharge plan for all customers; Concerns self with the safety of all Center residents in order to minimize the potential for fire and accidents. Also ensures that the Center adheres to legal, safety, health, fire, and sanitation codes by being familiar with his/her in carrying out the Center's fire, safety and disaster plans and by being familiar with current MSDS; Puts customer service first and adheres to the CareOne Culture of Excellence Pledge.
NewLead Vascular Sonographer Quality/IAC Technical Lead - $7,500 Sign-on Bonus! South Shore HealthLead Vascular Sonographer Quality/IAC Technical Lead - $7,500 Sign-on Bonus!Weymouth, MASee South Shore Health Privacy Policy at https://www.southshorehealth.org/website-privacy-policy and SonicJobs Privacy Policy at https://www.sonicjobs.com/us/privacy-policy and Terms of Use at https://www.sonicjobs.com/us/terms-conditions. Oversees the daily function and staffing needs of the department under the guidance and direction of the Vascular Ultrasound Supervisor, and the Executive Director of Diagnostic Imaging.
Director Supply Chain Healthcare JSADirector Supply Chain HealthcareFramingham, MA$75,000–$120,000 / yearFull timeDirects an organization's overall supply chain operations for a facility or multiple facilities, including purchasing, inventory and distribution of supplies and equipment. Ensures that issues regarding existing and new products are resolved in a timely and cost-efficient manner.
NewAssistant Director of Nursing, RN Linden Ponds by Erickson Senior LivingAssistant Director of Nursing, RNHingham, MA$120,000–$150,000 / yearLocation: Linden Ponds by Erickson Senior LivingJoin our team as the Assistant Director of Nursing is responsible for clinical leadership and outcomes within our Skilled, Assisted Living, and Memory Care neighborhoods. See Erickson Senior Living Privacy Policy at https://www.ericksonseniorliving.com/privacy-policy and SonicJobs Privacy Policy at https://www.sonicjobs.com/us/privacy-policy and Terms of Use at https://www.sonicjobs.com/us/terms-conditions.
NewDirector of Labor Relations Lesley UniversityDirector of Labor RelationsCambridge, MA$115,705–$131,392 / yearAt Lesley University we strive for a supportive and equitable environment where people -- regardless of race, ethnicity, color, sex, physical ability, religion, national origin or ancestry, age, neurodiversity, sexual orientation, gender identity or expression, genetic information, veteran or military status, membership in uniformed services, and all other categories protected by applicable state and federal laws -- can participate equally and fully as their true selves in all aspects of university life. In doing so, Lesley strives for a campus culture and community that fosters a true sense of belonging for all, provides opportunity for everyone to participate equally and fully in the Lesley experience, and helps to develop each individual's capacity to confidently and competently engage within and across difference.
NewEnterprise Solutions Director - Strategic Pursuits (RapidScale) Cox CommunicationsEnterprise Solutions Director - Strategic Pursuits (RapidScale)Boston, MA$148,500–$247,500This role partners closely with strategic Account Executives / Dealmakers to shape, qualify, and win RapidScale's largest and most complex opportunities-typically involving multi-year managed services, hybrid cloud transformations, carve-outs, divestitures, and Walk-In Takeovers (WITO). Role Overview: The Solution Director - Strategic Enterprise Pursuits is the senior authority responsible for owning complex enterprise solutions as commercially viable, operationally executable, and outcome-driven business constructs.
NewExecutive Director Sudbury Extended Day IncExecutive DirectorSudbury, MA$135,000–$150,000 / yearIdeal Candidate The successful candidate will be a mission-driven leader who brings: Experience leading teams and developing people Strong relationship-building and communication skills Strategic thinking balanced with operational excellence Financial and organizational management experience Ability to navigate complex stakeholder relationships with professionalism and empathy Commitment to high-quality programming and child-centered outcomes Knowledge of youth development, education, nonprofit management, or a related field Experience with multi-site operations and EEC regulations preferred Compensation & Benefits Full-time, exempt position Salary range: $135,000–$150,000 , commensurate with experience Annual performance-based bonus opportunity Comprehensive benefits package including health insurance, paid time off, retirement benefits, and professional development support To Apply Interested candidates should submit a resume and cover letter. The Executive Director oversees all aspects of organizational leadership, including: Strategic planning and organizational leadership Program quality and continuous improvement Staff leadership, development, and organizational culture Community engagement and stakeholder relations Financial management and operational oversight Regulatory compliance and risk management Partnership development and organizational sustainability The Executive Director maintains a visible presence throughout the organization and works closely with families, staff, school leaders, community partners, and the Board to ensure SED continues to deliver high-quality, safe, and engaging programs.
NewDirector - Product Development Ninja Indoor Heated SharkNinjaDirector - Product Development Ninja Indoor HeatedNEEDHAM, MA$123,800–$246,400 / yearSupport the Ninja business and the VP/SVP, Product Development with the development of successful and profitable programs for a full product category to ensure continued growth of the product portfolio – you will lead new product development (creation and management) of assigned product category from brainstorm phase through mass production, as well as partner with the VP/SVP to define the over-arching category roadmap direction to a team of product developers from entry through manager level. Powered by two trusted, global brands, Shark and Ninja, the company has a proven track record of bringing disruptive innovation to market and developing one consumer product after another has allowed SharkNinja to enter multiple product categories, driving significant growth and market share gains.
NewWine and Beverage Director Ci Siamo - BostonWine and Beverage DirectorBoston, MAEducate the Service Team on the wine, beer, spirits, cocktail, and non-alcoholic beverage offerings for all beverages within the restaurant in a way that adds quality and value as well as enhances the guest experience while achieving and surpassing financial goals . Located at Commonwealth Pier, an exciting new waterfront project within the Seaport neighborhood, Ci Siamo Boston looks forward to assembling a talented opening team in our new home.
NewSenior Director, Research and Development SharkNinjaSenior Director, Research and DevelopmentNEEDHAM, MA$161,500–$299,000 / yearPowered by two trusted, global brands, Shark and Ninja, the company has a proven track record of bringing disruptive innovation to market and developing one consumer product after another has allowed SharkNinja to enter multiple product categories, driving significant growth and market share gains. You will play a key leadership role within Engineering, partnering closely with Category, Design, Operations, Quality, Supply Chain, and Commercial teams to ensure alignment, prioritization, and successful product delivery.
NewNursing Director – Hematology/Oncology & Bone Marrow Transplant Tufts Medical CenterNursing Director – Hematology/Oncology & Bone Marrow TransplantBoston, MA$162,773.52–$207,541.52 / yearA management role that supervises employees focusing on tactical, operational activities within a specified area, with the majority of time spent overseeing area of responsibility, planning, prioritizing and/or directing the responsibilities of employees. Individual offers are determined using a comprehensive approach that considers relevant experience, certifications, education, skills, and internal equity to ensure compensation is fair, consistent, and aligned with our business goals.
Sr. Director of Quality Teledyne Technologies IncSr. Director of QualityBillerica, MA$188,000–$250,700 / yearOur products include advanced surveillance sensors, unmanned air and ground vehicles, sensing devices used to detect chemicals, biological agents, radiation and explosives, and a host of other solutions that help warfighters, first responders, and search-and-rescue teams do their jobs better. These markets include aerospace and defense, factory automation, air and water quality environmental monitoring, electronics design and development, oceanographic research, deepwater oil and gas exploration and production, medical imaging and pharmaceutical research.
Director of Quality Assurance Quality Engineering Plymouth Rock Management Company of New JerseyDirector of Quality Assurance Quality EngineeringBoston, MA$155,000–$205,000 / yearThis role will drive the strategy, execution and continuous improvement of testing practices across customer-facing and internal insurance platforms, ensuring high-quality, scalable, and reliable software delivery. The ideal candidate brings a strong track record of building and scaling test automation, improving engineering quality practices, and leading high-performing teams in an Agile environment.
NewDirector Of Quality Assurance - CMO/ CDMO RPM ReSearchDirector Of Quality Assurance - CMO/ CDMOWaltham, MassachusettsHas knowledge and skills across a range of Quality practices, procedures, and principles, with an astute ability to easily rank priorities based on importance and feel comfortable making decisions on quality issues. Demonstrate knowledge of and instruct department procedures and company policies, pay attention to detail in all areas, and ensure all the paperwork is completed completely, neatly, and fully.
Director of Quality Symmons Industries IncDirector of QualityBraintree, MAAs we design and redesign the minute details, we're also conscious of the bigger things, like water conservation, and energy reduction, and global impact. Our success is driven by our commitment to our core values: being customer-focused, embracing a can-do attitude, demonstrating resilience, and always striving to win as a team.
Director Head of GCPGVPGLP Quality Akebia Therapeutics IncDirector Head of GCPGVPGLP QualityCambridge, MA$199,555–$246,510 / yearBuild and maintain strong, collaborative relationships across key functions (e.g., Clinical Development, Clinical Operations, Biostatistics & Data Management, Pharmacovigilance/Drug Safety, and Nonclinical) to enable proactive quality oversight and execution of company objectives. The role is accountable for advancing and maturing the GCP, GVP, and GLP Quality function, ensuring high-quality, compliant execution of nonclinical and clinical programs from first-in-human studies through marketing authorization and post-marketing activities, as applicable.
Director of Quality Assurance and Regulatory Affairs Biomedical SearchDirector of Quality Assurance and Regulatory AffairsLittleton, MAThe Director will oversee Quality and Regulatory functions across multiple sites, ensuring compliance with FDA, ISO 13485, and other applicable regulations while partnering closely with Operations, Engineering, and Executive Leadership. This individual will play a key role in shaping quality strategy, strengthening the Quality Management System (QMS), leading audits and CAPA activities, and developing a high-performing QA/RA team.
Open Rank Clinical Professor and Director of Quality and Regulatory Compliance - School of Nursing Northeastern UniversityOpen Rank Clinical Professor and Director of Quality and Regulatory Compliance - School of NursingBoston, MA$101,000–$134,000 / yearDoctoral degree in Nursing or related field required • Minimum of 5 years of experience in nursing education • Demonstrated expertise in accreditation processes and regulatory compliance • Experience with curriculum development and program evaluation • Strong analytical skills and proficiency with data management systems • Excellent communication and collaborative leadership abilities • Active RN license and eligibility for state licensure. Please indicate how your experience, knowledge, and skills have prepared you to contribute to this work with written statements addressing the following prompts: • Teaching statement: Please summarize your past instructional and mentorship experiences, your pedagogical philosophy, your plans/goals for teaching in the College of Science (including existing and proposed courses), and your strategies for teaching and mentoring global student populations.
Senior Quality Director Nova Biomedical CorpSenior Quality DirectorWaltham, MA$220,000–$300,000 / yearThe Senior Director of Quality focuses on assuring company compliance to ISO/FDA QSR, IVDD, IVDR, ISO 13485, ISO 14971; Direct oversight of CAPA management, ISO/QSR employee training; metrics; validation, internal and external quality auditing processes; improvements. With headquarters in Norwood and Waltham, Massachusetts, and a global team of nearly 2,000 employees, were building a collaborative, empowered culture grounded in shared values: Customer Centricity, Ingenuity, Ownership & Accountability, Collaboration, and Integrity.
Executive Director, Quality and Safety Lahey Hospital and Medical CenterExecutive Director, Quality and SafetyBeverly, MA$187,200–$228,800 / yearTeam Leadership and Management: • Manage and mentor a team of professionals, including the Performance Improvement project managers, Quality/Safety site leaders, the Patient Experience Manager and the Regulatory and Patient Safety Manager. Over-Arching Goals: The Executive Director will oversee and ensure that the Hospitals follow the overarching goals of quality and safety to provide high quality, patient-centered care while ensuring the safety and well-being of patients, healthcare providers, and staff.
Director of Quality, Compliance and Audit PhilipsDirector of Quality, Compliance and AuditCambridge, MAYour role: Compliance Engineering • Owns the global Compliance Engineering function, integrating CAPA, root cause analysis, risk management, and systemic issue prevention • Drives proactive identification and mitigation of compliance risks across the QMS • Ensures robust problem-solving methodologies are consistently applied (e.g., 5 Whys, Fishbone, Fault Tree, statistical analysis) • Leads governance forums to review systemic issues, trends, and escalations • Ensures CAPA remains effective as a subset of the broader Compliance Engineering framework. People Leadership & Organizational Development • Leads and develops a global team of compliance engineers and audit professionals • Ensures appropriate resource allocation, workload balance, and technical capability • Builds succession plans and develops specialized compliance and engineering skillsets • Ensure team performance and talent retention, as well as improving employee engagement scores • Owns annual budget for Internal Audit & Compliance Engineering function • Optimizes cost vs.
Director of Quality Management (RN) | Stoughton Specialty PAM Health Specialty Hospital of StoughtonDirector of Quality Management (RN) | Stoughton SpecialtyStoughton, Massachusetts$100,000–$125,000 / yearFull timePAM Health is committed to providing high-quality patient care and outstanding customer service, coupled with the loyalty and dedication of highly trained staff, to be the most trusted source for post-acute services in every community it serves. About PAM Health: PAM HEALTH (PAM) based in Enola, Pennsylvania, provides specialty healthcare services through more than 80 locations, as well as wound clinics and outpatient physical therapy locations, in 17 states.
Senior Director, Quality Systems Kailera TherapeuticsSenior Director, Quality SystemsWaltham, MassachusettsThe Senior Director, Quality Systems is a high-impact leadership role responsible for the architecture, implementation, and continuous improvement of our Enterprise Quality Management System (eQMS). Proven track record in mid-sized companies navigating the transition from early-phase clinical trials to late-stage pivotal studies.
Associate Director, Quality Control Technical Services Beam TherapeuticsAssociate Director, Quality Control Technical ServicesCambridge, MA$185,000–$225,000 / yearThe successful candidate will work cross‑functionally with Analytical Research & Development, Bioprocess Development, Manufacturing Technical Services, Manufacturing Operations, Regulatory Affairs, and Quality Assurance to drive the transfer, qualification, validation, and lifecycle management of analytical methods for gene‑edited cell therapy products and associated critical materials (e.g., mRNA). In addition, this position will contribute directly to regulatory filings, including specifications, analytical method validation reports, and CMC documentation, and will serve as a QC technical subject matter expert across program teams to ensure compliant, robust, and phase‑appropriate analytical strategies.
Director, Quality Control Oruka TherapeuticsDirector, Quality ControlWaltham, CaliforniaThe Director, Quality Control – Combination Products will provide strategic and operational leadership for the Quality Control function supporting late-stage clinical development, analytical testing oversight for clinical drug substance and drug product, process performance qualification (PPQ), regulatory submissions, and commercial launch readiness for monoclonal antibody drug products and combination products, including pre-filled syringes and autoinjectors. Strong knowledge of cGMP regulations and global regulatory expectations, including 21 CFR Parts 210, 211, and 4. Hands-on experience supporting combination products such as pre-filled syringes, autoinjectors, or related delivery systems.
Senior Director, Quality Control Obsidian Therapeutics IncSenior Director, Quality ControlBedford, MA$232,000–$280,000 / yearAs a key contributor within the Technical Operations Team and player-coach, you will lead Quality Control activities supporting the development of our first clinical-stage autologous cell therapy program targeting solid tumors and drive a culture of rigorous thinking, exceptional collaboration and transparency, continuous learning, and outcomes focus. Develop and support a high performing team to execute department responsibilities; ensure effective utilization of resources through strong people leadership including consistent performance management, robust employee engagement and development, and philosophically aligned rewards and recognitions practices.
Director, GMP Quality Assurance Oruka TherapeuticsDirector, GMP Quality AssuranceWaltham, CaliforniaReview and approve GMP documentation, including master batch records, executed batch records, analytical methods, specifications, validation protocols and reports, tech transfer documentation, stability protocols and reports, and risk-assessment documentation. Oruka’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.
NewQuality Director, Single Use Division - Flexible Operations Sites Thermo Fisher Scientific IncQuality Director, Single Use Division - Flexible Operations SitesWaltham, MA$160,000–$218,250 / yearThe Quality Director for the Single Use Division (SUD) Flexible Operations Sites is responsible for leading and advancing the quality strategy, culture, compliance, and operational excellence across multiple manufacturing and operations sites supporting flexible single-use technologies and products. We provide our global teams with the resources needed to achieve individual career goals while helping to take science a step beyond by developing solutions for some of the world's toughest challenges, like protecting the environment, making sure our food is safe or helping find cures for cancer.
Associate Director, Global Quality Risk Management Biogen IncAssociate Director, Global Quality Risk ManagementMA$155,000–$214,000 / yearp>Regular 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. Reporting to the Director of Quality Risk Auditing & Governance, you will be the primary enterprise lead for the execution of QRM, ensuring that risk-based thinking is interwoven into our Quality Management System (QMS), operational decision-making processes, and organizational culture.
Director, Quality Engineering MKS IncDirector, Quality EngineeringWilmington, MA$168,300–$280,500 / yearLeveraging deep expertise in quality assurance, process optimization, and complex assembly manufacturing, you will develop and implement strategic quality objectives to enhance product quality, reliability, compliance and efficiency. We win as a team and are committed to recruiting and hiring qualified applicants regardless of race, color, national origin, sex (including pregnancy and pregnancy-related conditions), religion, age, ancestry, physical or mental disability or handicap, marital status, membership in the uniformed services, veteran status, sexual orientation, gender identity or expression, genetic information, or any other category protected by applicable law.
Quality Compliance Director Old Colony Elder ServicesQuality Compliance DirectorBrockton, MAFull timeOur mission: Through the talents of an experienced and diverse workforce, OCES supports the independence and dignity of older adults and individuals with disabilities by providing essential information and services that promote healthy, safe living which positively impacts our community. By promoting healthy, safe living for our consumers, we hope to allow them to stay active and engaged in their lives and in their own communities for as long as possible.
Director, Global Quality Systems and Compliance Scholar Rock Holding CorpDirector, Global Quality Systems and ComplianceCambridge, MAScholar Rock is a late-stage global biopharmaceutical company focused on developing and commercializing apitegromab for children and adults with spinal muscular atrophy (SMA) and other rare, severe, and debilitating neuromuscular diseases. Optimize core QMS processes (change control, deviations, CAPAs, complaints, audits, document control, training, and supplier quality) to ensure they are efficient, phase-appropriate, and scalable for commercial operations.
Director, CMC QA Korro Bio IncDirector, CMC QACambridge, MA$200,000–$240,000 / yearPosition Summary: The Director, CMC QA will be responsible for providing quality oversight and direction to Korro Bio''s vendors to ensure that drug substance, drug product, and finished product are manufactured, tested, released, and distributed in compliance with current Good Manufacturing Practices (cGMPs). Provide quality and technical input to cross-functional project teams, and review internal and external documentation including protocols, reports, test methods, specifications, master batch records, and SOPs.
Director, Clinical Quality Control Disc Medicine IncDirector, Clinical Quality ControlMA$198,000–$242,000 / yearAct as the team leader to ensure alignment and effective communication among cross-functional areas, including analytical development, process development, formulation development, manufacturing, supply chain, regulatory, quality assurance, and other internal and external partners. Ability to work both independently and collaboratively with project teams and cross-functionally, to build productive relationships with internal and external partners, to influence decision-making, and to engage in conflict resolution.
Associate Director, Analytical Development & Clinical Quality Control Disc Medicine IncAssociate Director, Analytical Development & Clinical Quality ControlMA$158,000–$193,000 / yearAct as the team leader to ensure alignment and effective communication among cross-functional areas, including analytical development, process development, formulation development, manufacturing, supply chain, regulatory, quality assurance, and other internal and external partners. Ability to work both independently and collaboratively with project teams and cross-functionally, to build productive relationships with internal and external partners, to influence decision-making, and to engage in conflict resolution.
NewDirector, Quality Assurance SS&C Technologies Holdings IncDirector, Quality AssuranceBoston, MAEstablish AI best practices for the QA team, develop a QA AI training program and knowledge sharing, head a technical QA leadership cohort to oversee AI POCs and projects across the QA team, and to explore new uses and applications of AI to improve quality and efficiency. Unless explicitly requested or approached by SS&C Technologies, Inc. or any of its affiliated companies, the company will not accept unsolicited resumes from headhunters, recruitment agencies, or fee-based recruitment services.
Director, Data Quality IQVIA Holdings IncDirector, Data QualityBurlington, MA$110,200–$307,200 / yearCedar Gate Technologies, an IQVIA business, is hiring a Director of Data Quality to lead data quality strategies within a complex healthcare data environment, and to modernize data quality processes using Agentic AI and intelligent automation. In addition, this role serves as a Subject Matter Expert in Agentic AI frameworks and AI-driven data quality capabilities, responsible for advancing the organization's use of automation and AI to scale and modernize data quality operations.
Associate Director, Product Quality Assurance Beam TherapeuticsAssociate Director, Product Quality AssuranceCambridge, MA$185,000–$225,000 / yearWorking closely with the assigned PQLs, the role supports consistency and quality of content and product strategy across the CMC spectrum including review of CMC technical content provided for global clinical and commercial regulatory submissions as well as associated quality records. Beam's suite of gene editing technologies is anchored by base editing, a proprietary technology that is designed to enable precise, predictable and efficient single base changes, at targeted genomic sequences, without making double-stranded breaks in the DNA.
Director, Clinical Quality Assurance Oruka TherapeuticsDirector, Clinical Quality AssuranceWaltham, MassachusettsRemoteThis role will establish, improve, and lead phase-appropriate clinical quality processes, ensure robust oversight of clinical trial execution and vendor performance, and drive inspection readiness for global health authority inspections, including FDA Bioresearch Monitoring (BIMO) inspections. The Director, Clinical Quality Assurance is responsible for providing strategic quality leadership, support, and oversight for Oruka’s clinical development activities, with primary focus on Good Clinical Practice (GCP) and related quality systems supporting clinical trials.
Director, Product Quality Kymera TherapeuticsDirector, Product QualityWatertown, MA$195,000–$275,000 / yearFor more information about our science, pipeline and people, please visit www.kymeratx.com or follow us on X (formerly Twitter) or LinkedIn. Having advanced the first degrader into the clinic for immunological diseases, Kymera is focused on building an industry-leading pipeline of oral small molecule degraders to provide a new generation of convenient, highly effective therapies for patients with these conditions.
NewAssociate Director, Quality Compliance Genetix BiotherapeuticsAssociate Director, Quality ComplianceSomerville, MassachusettsThe Associate Director, Quality Compliance is a key member of the QA Compliance organization, responsible for ensuring quality oversight of regulatory submissions and lifecycle management for Genetix Biotherapeutics (GTX) products. Additionally, the Associate Director partners cross-functionally and with external vendors to support health authority inspection readiness activities, mock inspections and internal audits.
Associate Director, Quality Control Technical Services Beam Therapeutics IncAssociate Director, Quality Control Technical ServicesCambridge, MA$185,000–$225,000 / yearThe successful candidate will work cross-functionally with Analytical Research & Development, Bioprocess Development, Manufacturing Technical Services, Manufacturing Operations, Regulatory Affairs, and Quality Assurance to drive the transfer, qualification, validation, and lifecycle management of analytical methods for gene-edited cell therapy products and associated critical materials (e.g., mRNA). Primary Responsibilities: Lead and influence QC CMC strategy in partnership with cross-functional CMC teams for master cell banks (MCBs), plasmids, and mRNA drug substance and critical materials, supporting both ex vivo and in vivo therapy programs across development and commercialization.
Director of Compliance, Quality & Risk- Home Care & Hospice Lowell General HospitalDirector of Compliance, Quality & Risk- Home Care & HospiceLowell, MA$134,525.66–$171,524.44 / yearResponsibilities typically include: ownership of short to mid-term (1-3 years) execution of functional strategy and the operational direction of the Department, problems faced are often complex and require extensive investigation and analysis, and requires ability to influence others to accept practices and approaches, and ability to communicate and influence executive leadership. A management role that supervises employees focusing on tactical, operational activities within a specified area, with the majority of time spent overseeing area of responsibility, planning, prioritizing and/or directing the responsibilities of employees.