Director of Data Governance and Quality JobotDirector of Data Governance and QualityWorcester, MA$150,000ā$200,000 / yearInformation collected and processed as part of your Jobot candidate profile, and any job applications, resumes, or other information you choose to submit is subject to Jobot's Privacy Policy, as well as the Jobot California Worker Privacy Notice and Jobot Notice Regarding Automated Employment Decision Tools which are available at jobot.com/legal. Strong communication skills, with the ability to effectively communicate complex data concepts to non-technical stakeholders.
Quality Director Micro TechQuality DirectorWestborough, MAli>Collaborate with engineering, production, and supply chain teams to support design for manufacturability, process validation, and continuous improvement initiatives. Oversee all quality assurance and quality control activities across the manufacturing process, including incoming inspections, in-process checks, and final product verification.
Director of Social Services Care-OneDirector of Social ServicesLowell, 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.
NewDirector of Diagnostic Imaging - Direct Placement TalentBurst, Inc.Director of Diagnostic Imaging - Direct PlacementAttleboro, MA$118,292.77ā$185,597.27 / yearThis leadership role requires extensive experience in imaging, strong management skills, and thorough knowledge of various imaging modalities to include X-RAY, IR, CT, MRI, Mammography, Ultrasound, Nuclear Medicine and Vascular Services. Leads and manages daily operations of Diagnostic and Interventional Radiology, Vascular, MRI, CT, Ultrasound, Mammography, and Nuclear Medicine, ensuring efficient, high-quality services to meet patient and physician need.
NewDirector - Product Development Ninja Indoor Heated SharkNinjaDirector - Product Development Ninja Indoor HeatedNeedham, MA$123,800ā$246,400 / yearul>Support 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 ā 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.
Director Supply Chain Healthcare JSADirector Supply Chain HealthcareFramingham, MA$75,000ā$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.
Medical Director in Worcester, MA TeamHealthMedical Director in Worcester, MAWorcester, MA$359,200ā$474,000 / yearFull timeThis role offers a balanced mix of hands-on clinical care and administrative leadership, with the opportunity to partner closely with hospital leadership to drive quality outcomes, operational efficiency, and patient experience initiatives. California Applicant Privacy Act: https://www.teamhealth.com/california-applicant-privacy-notice/
Anesthesiology Medical Director in Leominster, MA TeamHealthAnesthesiology Medical Director in Leominster, MALeominster, MA$500,000ā$550,000 / yearFull timeStep into a leadership role as a facility medical director with TeamHealth, where you'll have the opportunity to guide a dedicated team, shape the delivery of high-quality patient care, and make a meaningful, lasting impact within a collaborative and supportive environment. The ideal candidate will be a board-certified anesthesiologist who possess outstanding communication skills and demonstrates leadership qualities, all while being committed to professional development and creating a desirable workplace environment.
NewOB Hospitalist - Director Opportunity - Worcester OptigyOB Hospitalist - Director Opportunity - WorcesterWorcester, MAli>Highly relational, able to build strong rapport and positive working relationships with all stakeholders (Hospital leadership, hospitalist teams, nurses, staff physicians, and OBHG corporate staff). Will collaborate with the MMD, MDO or VPCO to ensure the clinical team is delivering a quality program that achieves both OBHG's and the hospital's clinical and operational objectives.
NewExecutive Director Sudbury Extended Day IncExecutive DirectorSudbury, MA$135,000ā$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: $135,000ā$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.
Medical Device - Director of Operations - Sturbridge, MA Michael Page USAMedical Device - Director of Operations - Sturbridge, MASturbridge, MA$180,000ā$195,000 / yearFull timeYou will lead cross-functional teams, optimize production, and implement continuous improvement initiatives to enhance capacity, quality, and delivery in a highly regulated environment. With a strong international footprint, the organization delivers complex, life-enhancing products through advanced manufacturing technologies and operational excellence.
NewDirector of Sales & Marketing - Assisted Living Notre Dame Health Care Center, Inc.Director of Sales & Marketing - Assisted LivingGreendale, MA$79,000ā$95,000 / yearProficiency in Microsoft suite, electronic formats, and database systems Possessing a valid driverās license, and a reliable and insured vehicle Ability to flex schedule to attend pertinent evening events and participate in Manager on Duty weekend rotation Compensation details: 79000-95000 Yearly Salary PI187055cf7f2e-25448-404906435c143e31-5e48-4549-b638-05792d185386 Responsibilities include the development and execution of du Lac Assisted Living's marketing plan, managing digital marketing campaigns, attending professional networking and community events, fielding inquiry calls, conducting residence tours, generating admissions for the assisted living community, and attending industry related continuing education seminars.
Director of Quality Improvement StrivectorDirector of Quality ImprovementWorcester, MAb>POSITION OVERVIEWAs a Director of Quality Improvement your roles and responsibilities will include: Responsible for leading the Quality / Performance Improvement activities across the hospital. Strivector has been consistently rated a rare 4.6/5 on Google, Indeed and Glassdoor by our candidates, customers, employees and contractors.Elevate your professional journey with us.
Senior Quality Director Nova BiomedicalSenior Quality DirectorWaltham, MA$220,000ā$300,000 / yearReggiannini%40aicompanies.com%7Cf6fba6f305dd4f5db48208dd4cfb41b1%7Cef83c7bf14e34752af743ef60a50e893%7C0%7C0%7C638751364205790035%7CUnknown%7CTWFpbGZsb3d8eyJFbXB0eU1hcGkiOnRydWUsIlYiOiIwLjAuMDAwMCIsIlAiOiJXaW4zMiIsIkFOIjoiTWFpbCIsIldUIjoyfQ%3D%3D%7C0%7C%7C%7C&sdata=EsnZO9uH6fllGdFfgcxIXEsPp3qEXFI%2FT5rnvjqL6MU%3D&reserved=0" rel="nofollow noopener noreferrer" target="_blank">https://advancedinstruments.showpad.com/share/DmsEd5QTLlqemTYABlvDW. The 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.
Site Quality Director VulcanForms IncSite Quality DirectorMA$185,000ā$250,000 / yearp>As the Site Quality Director at VulcanForms, your mission is to build and lead the Quality organization for a new, advanced manufacturing facility focused on mass-production, 3D-printed titanium components for a high-volume consumer electronics program. Operating within a fast-paced Business Unit (BU) model, you will directly govern the site's execution, inspection, and lab infrastructure - rapidly scaling the organization to support maximum facility footprint and full mass-production capacity.
Director of Quality Improvement Veracity Software IncDirector of Quality ImprovementWorcester, MAYes/No ā details): Experience leading hospital-wide Quality Improvement and Patient Safety programs (Yes/No ā details): Experience with Joint Commission, CMS, and regulatory survey readiness (Yes/No ā details): Experience managing Performance Improvement initiatives and data reporting (Yes/No ā details): Experience promoting a Culture of Safety and Patient Safety programs (Yes/No ā details): Experience overseeing Quality/PI staff and department operations (Yes/No ā details): Experience working with Medical Staff and hospital leadership on quality outcomes (Yes/No ā details): Experience with accreditation, compliance, and regulatory requirements (Yes/No ā details): Motivation / Reason for Relocation (if not local): Motivation / Reason for interest in this position: Contact Number: Email ID: LinkedIn Profile URL: Full Address (Street, City, State, Zip Code): Notice Period (in weeks): Current Work Authorization Status: Expected Salary: Are you able to relocate on your own expenses and work onsite at Worcester, MA?. The individual in this position is a key member of the hospital management team, and provides leadership and oversight to the strategic development and implementation of the quality and patient safety programs (performance improvement, patient safety, and accreditation) with responsibility for planning, organizing, directing the managerial and operational activities of the infrastructure required to support these services.
Sr. Director of Quality Teledyne Technologies IncSr. Director of QualityBillerica, MA$188,000ā$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 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.
RN RT PT OT Director of Quality/Risk Management Vibra Healthcare LLCRN RT PT OT Director of Quality/Risk ManagementMAResponsibilities Responsible for directing quality management efforts to ensure continuous improvement and organizational excellence, adherence with all regulatory, compliance, accreditation, and legal issues, and promote a safe environment for all employees, patients and visitors. Hospital Details Vibra Hospital of Western Massachusetts - Central Campus, located in Rochdale, MA is a 47 bed Critical Care Hospital providing acute care services to patients recovering from serious illnesses or injuries.
Director of Quality Improvement Macpower Digital Assets Edge Private LimitedDirector of Quality ImprovementWorcester, MA$128,000ā$198,000 / yeardiv style="text-align:justify">The individual in this position is a key member of the hospital management team, and provides leadership and oversight to the strategic development and implementation of the quality and patient safety programs (performance improvement, patient safety, and accreditation) with responsibility for planning, organizing, directing the managerial and operational activities of the infrastructure required to support these services. Required Qualifications:Education: Registered Professional Nurse (RN) with Bachelor, Master, or Doctorate degree inpatient care related field.
Director of Quality Improvement Saint Vincent HospitalDirector of Quality ImprovementWorcester, MAThe individual in this position is a key member of the hospital management team, and provides leadership and oversight to the strategic development and implementation of the quality and patient safety programs (performance improvement, patient safety, and accreditation) with responsibility for planning, organizing, directing the managerial and operational activities of the infrastructure required to support these services. Healthgrades awarded Saint Vincent Hospital #1 in Cardiology in the state and one of Americas 100 Best Hospitals for Coronary Intervention in 2023 and 2024, which puts Saint Vincent Hospital in the top 5% of hospitals nationwide for coronary intervention.
Director of Quality Improvement Metrowest Medical CenterDirector of Quality ImprovementTown of Framingham, MassachusettsAt Framingham Union Hospital, youll find comprehensive health care services for the entire family including 24-hour emergency care, advanced cardiac care, high-tech cancer treatments and advanced maternity care including our Special Care Level IIB nursery and high-risk pregnancy care. The individual in this position is a key member of the hospital management team, and provides leadership and oversight to the strategic development and implementation of the quality and patient safety programs (performance improvement, patient safety, and accreditation) with responsibility for planning, organizing, directing the managerial and operational activities of the infrastructure required to support these services.
Senior Director, Quality Systems Kailera TherapeuticsSenior Director, Quality SystemsWaltham, Massachusettsp>The 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). At Kailera, we are bold, authentic and committed to our mission of developing therapies that give people the power to transform their lives and elevate their overall health.Director of Quality & Reliability Engineering Boston Materials, IncDirector of Quality & Reliability EngineeringBillerica, MA$180,000ā$230,000 / yearp>In this role, you will lead and advance the Quality function at Boston Materials, ensuring our products, processes, and data consistently meet the expectations of the most demanding advanced semiconductor and AI datacenter customers. You will work directly alongside Product Development and Manufacturing to evaluate data, build systems, challenge assumptions, and ensure corrective actions are real and durable.Director, Quality Control Oruka TherapeuticsDirector, Quality ControlWaltham, Californiap>The Director, Quality Control ā 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$232,000ā$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, Californiali>Review 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. Orukaās 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.Quality Director Ignite Human CapitalQuality DirectorWestborough, Massachusettsli>Serve as the executive quality leader for ISO-certified quality management systems, including ISO 9001, ISO 13485, AS9100, and support environmental management initiatives aligned with ISO 14001. The ideal leader brings a balance of executive-level strategic thinking and practical execution, with deep expertise in regulated manufacturing environments, supplier quality, process optimization, and cross-functional leadership.Director, Quality Control TScan TherapeuticsDirector, Quality ControlWaltham, MA$210,000ā$220,000 / yearThe submission of unsolicited resumes by recruitment or staffing agencies to TScan Therapeutics or its employees is strictly prohibited unless contacted directly by TScan Therapeuticsā internal Talent Acquisition team. Reporting to the Associate Vice President of QC and AD, the ideal candidate should have relevant experience in compendial, cellular, molecular, and environmental monitoring in a cGMP facility, and enjoy fast-paced, collaborative, and vibrant culture.Director of Quality Improvement Tenet Healthcare CorpDirector of Quality ImprovementWorcester, MAp>The individual in this position is a key member of the hospital management team, and provides leadership and oversight to the strategic development and implementation of the quality and patient safety programs (performance improvement, patient safety, and accreditation) with responsibility for planning, organizing, directing the managerial and operational activities of the infrastructure required to support these services. Healthgrades awarded Saint Vincent Hospital #1 in Cardiology in the state and one of Americas 100 Best Hospitals for Coronary Intervention in 2023 and 2024, which puts Saint Vincent Hospital in the top 5% of hospitals nationwide for coronary intervention.Director, Quality Electric Hydrogen CoDirector, QualityMA$192,270ā$226,200 / yearli>Operationalize and continuously improve core quality processes, including Non-Conformance Reporting (NCR), Incoming Quality Control (IQC), Material Review Board (MRB), and Corrective and Preventive Actions (CAPA). Professional certifications such as ASQ CQE, CQA, CMQ/OE, Lean Six Sigma Black Belt, ISO Lead Auditor, or equivalent quality certifications strongly preferred.Director_Manufacturing Quality Consultant_ Life Sciences PricewaterhouseCoopers LLPDirector_Manufacturing Quality Consultant_ Life SciencesMA$155,000ā$410,000 / yearDemonstrates some proven abilities to collaborate and work with a diverse team including: Basic problem solving and analysis skills; Financial modeling skills; Basic spreadsheet, presentation and document development skills; Demonstrates the ability to build, maintain, and utilize networks of client relationships; Interpersonal skills and proactive communication; and, Collaborative and "can-do" mindset eager to take on challenges. PwC does not intend to hire experienced or entry level job seekers who will need, now or in the future, PwC sponsorship through the H-1B lottery, except as set forth within the following policy: https://pwc.to/H-1B-Lottery-Policy.Sr. Director, Supply Chain QA Ultragenyx Pharmaceutical IncSr. Director, Supply Chain QABedford, MA$251,300ā$310,500 / yearThe successful candidate will bring deep hands-on experience with global GDP requirements, temperature controlled supply chains, and complex international distribution networks, and will serve as the quality authority for supply chain operations across internal teams and external partners. Ultragenyx is seeking an experienced Senior Director, Supply Chain Quality to provide global quality leadership and oversight across packaging, labeling, global logistics, distribution, and external supply chain partners supporting both clinical and commercial products.Associate Director, Head of IMP Quality Takeda Pharmaceutical Co LtdAssociate Director, Head of IMP QualityLexington, MA$153,600ā$241,340 / yearThe 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. Takeda is seeking an experienced Associate Director, Head of IMP Quality to lead quality operations for investigational medicinal products (IMPs) from clinical development through to commercialization.Director, Quality Control Oruka Therapeutics IncDirector, Quality ControlWaltham, MA$213,000ā$240,000 / yearRole Overview: The 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.Director of Quality- Grafton and Dillon Precision Castparts CorpDirector of Quality- Grafton and DillonMAp>for description go through this url https://pcctalentacquisitionportal.tal.net/vx/mobile-0/appcentre-ext/brand-7/candidate/so/pm/1/pl/3/opp/22565-Director-of-Quality-Grafton-and-Dillon/en-GB.Program Director, Knowledge & QA BullhornProgram Director, Knowledge & QAMassachusettsp>The Program Director, Knowledge & QA is a new, high-visibility individual contributor role that will own the design, execution, and continuous improvement of Bullhorn's Knowledge-Centered Service (KCS) program and Global Support Quality Assurance (QA) program. Bullhorn's core purpose is to create an incredible customer experience, and the organization has a sharp focus on delivering very high quality products and services to its customers.Quality Director (24568) Natel Engineering Co. Inc. (Inactive)Quality Director (24568)Westborough, MAp>Benefits Offered: Comprehensive benefit package including medical, dental and vision coverage; company-paid basic life/AD&D insurance, short-term and long-term disability insurance; voluntary supplemental insurances, flexible spending accounts and employee assistance program (EAP). Summary: Manage the quality organization, develop quality policies, generate quality reports and provide support to organizations within the Company on quality-related issues.Director, GMP Quality Assurance Oruka Therapeutics IncDirector, GMP Quality AssuranceWaltham, MA$213,000ā$240,000 / yearReview 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.Director, Pharmacovigilance Quality Assurance Dyne Therapeutics IncDirector, Pharmacovigilance Quality AssuranceWaltham, MA$190,000ā$232,800 / yearThis role leads the design and execution of Dyne's Pharmacovigilance Quality Management System (QMS), including policies, procedures, audits, inspections, inspection readiness, and vendor oversight, to ensure PV systems and processes meet global regulatory requirements and support high-quality regulatory submissions. The company is advancing clinical programs for Duchenne muscular dystrophy (DMD) and myotonic dystrophy type 1 (DM1) as well as a preclinical programs for facioscapulohumeral muscular dystrophy (FSHD) and Pompe disease.Senior Director Quality Assurance Filtration Danaher CorpSenior Director Quality Assurance FiltrationMarlborough, MA$215,000ā$250,000 / yearli>Demonstrated understanding of root cause analysis, corrective and preventive action (CAPA), change control, verification and validation methodologies, manufacturing/production process control methodologies, risk management, and continuous improvement in a medical device environment. What you will do: Partner with the Global QARA leaders and the Filtration leadership to drive functional initiatives, supportive of the business priorities, enabling business strategy and growth.Director, Quality Control TScan Therapeutics IncDirector, Quality ControlWaltham, MA$210,000ā$220,000 / yearThe submission of unsolicited resumes by recruitment or staffing agencies to TScan Therapeutics or its employees is strictly prohibited unless contacted directly by TScan Therapeutics internal Talent Acquisition team. Reporting to the Associate Vice President of QC and AD, the ideal candidate should have relevant experience in compendial, cellular, molecular, and environmental monitoring in a cGMP facility, and enjoy fast-paced, collaborative, and vibrant culture.Assoc. Director, Quality - Commercial Kiniksa Pharmaceuticals International PlcAssoc. Director, Quality - CommercialLexington, MA$186,000ā$200,000 / yearp>The Associate Director, Quality is responsible for providing quality leadership and oversight for all GMP technical transfer activities, including process transfer from development to commercial manufacturing, siteātoāsite transfers, and CMO/CDMO technology transfers. Execute and support GMP quality Systems, including deviations, investigations, CAPA's, change control, batch review, CPV, OOS/OOT management, and stability programs, ensuring timely and compliant closure.Director, Quality Management Systems Dyne Therapeutics IncDirector, Quality Management SystemsWaltham, MA$196,000ā$230,000 / yearThis role is responsible for key elements of the QMS including supplier quality, audits, and product complaint management programs, ensuring these systems are inspection-ready, risk-based, and aligned with global regulatory expectations. Role Summary: The Director, Quality Management Systems is a quality leader responsible for designing, scaling, and advancing a global Quality Management System (QMS) that supports Dyne's transition to commercial operations.Director, Quality Microbiology Integra LifeSciences Holdings CorpDirector, Quality MicrobiologyMA$166,750ā$228,850 / yearp>ESSENTIAL DUTIES AND RESPONSIBILITIES. To perform this job successfully, an individual must be able to perform each essential duty satisfactorily: Provide technical talent training, mentoring, and development support for microbiology personnel and cross-functional teams. The candidate must be an experienced team leader who leverages the talent of their team to increase performance, generate results, and maintain robust quality of manufacturing site microbiology programs.Director, Quality Systems (Remote) Steris PlcDirector, Quality Systems (Remote)Northborough, MARemote$144,500ā$187,000 / yearThe Director, Quality Systems leads teams of Senior Quality Managers, Quality Managers, Analysts/Engineers, and Technicians responsible for product quality, product release, supplier quality, continuous improvement support, technical support/technical guidance, and quality system execution. The Director, Quality Systems is responsible for leading, planning, developing, and directing quality operations policies, programs, initiatives, and overall execution of the STERIS QMS within multiple facilities spread across geographical regions and countries.Director, Clinical Quality TScan TherapeuticsDirector, Clinical QualityWaltham, MA$217,500ā$230,000 / yearli>Quality Assurance Activities:Conduct GCP audits, including investigator sites, clinical vendors, and clinical systems such as trial master files, clinical databases, pharmacovigilance, etc. The ideal candidate will possess deep expertise in quality assurance within clinical research, a strong understanding of the regulatory landscape for cell and gene therapy, and the ability to collaborate effectively across cross-functional teams.Sr. Director, External Manufacturing Quality, Cell Therapy Bristol-Myers Squibb CoSr. Director, External Manufacturing Quality, Cell TherapyMA$238,200ā$288,637 / yearp>To define and shape the Quality strategy for global Contract Manufacturing Organizations (CMO) and associated Contract Test Labs (CTLs) management for the Cell Therapy External Manufacturing (ExM) network and to ensure a high level of cGMP compliance and the safety, efficacy, and quality of externally manufactured commercial products. To build relationships with senior leadership in the CMO and CTL network to support the Virtual Plant Teams (VPTs) and Virtual Analytical Teams (VATs) and to proactively manage and improve CMO Quality performance through risk-based oversight and periodic reviews.12345678910Similar Job SearchesDirector Of Quality JobsDirector Of Quality Management JobsLine Leader JobsMaintenance Worker JobsProduction Manager JobsQuality Assurance JobsQuality Control Manager JobsQuality Coordinator JobsQuality Manager JobsQuality Specialist Jobs
Director of Quality & Reliability Engineering Boston Materials, IncDirector of Quality & Reliability EngineeringBillerica, MA$180,000ā$230,000 / yearp>In this role, you will lead and advance the Quality function at Boston Materials, ensuring our products, processes, and data consistently meet the expectations of the most demanding advanced semiconductor and AI datacenter customers. You will work directly alongside Product Development and Manufacturing to evaluate data, build systems, challenge assumptions, and ensure corrective actions are real and durable.
Director, Quality Control Oruka TherapeuticsDirector, Quality ControlWaltham, Californiap>The Director, Quality Control ā 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$232,000ā$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, Californiali>Review 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. Orukaās 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.
Quality Director Ignite Human CapitalQuality DirectorWestborough, Massachusettsli>Serve as the executive quality leader for ISO-certified quality management systems, including ISO 9001, ISO 13485, AS9100, and support environmental management initiatives aligned with ISO 14001. The ideal leader brings a balance of executive-level strategic thinking and practical execution, with deep expertise in regulated manufacturing environments, supplier quality, process optimization, and cross-functional leadership.
Director, Quality Control TScan TherapeuticsDirector, Quality ControlWaltham, MA$210,000ā$220,000 / yearThe submission of unsolicited resumes by recruitment or staffing agencies to TScan Therapeutics or its employees is strictly prohibited unless contacted directly by TScan Therapeuticsā internal Talent Acquisition team. Reporting to the Associate Vice President of QC and AD, the ideal candidate should have relevant experience in compendial, cellular, molecular, and environmental monitoring in a cGMP facility, and enjoy fast-paced, collaborative, and vibrant culture.
Director of Quality Improvement Tenet Healthcare CorpDirector of Quality ImprovementWorcester, MAp>The individual in this position is a key member of the hospital management team, and provides leadership and oversight to the strategic development and implementation of the quality and patient safety programs (performance improvement, patient safety, and accreditation) with responsibility for planning, organizing, directing the managerial and operational activities of the infrastructure required to support these services. Healthgrades awarded Saint Vincent Hospital #1 in Cardiology in the state and one of Americas 100 Best Hospitals for Coronary Intervention in 2023 and 2024, which puts Saint Vincent Hospital in the top 5% of hospitals nationwide for coronary intervention.
Director, Quality Electric Hydrogen CoDirector, QualityMA$192,270ā$226,200 / yearli>Operationalize and continuously improve core quality processes, including Non-Conformance Reporting (NCR), Incoming Quality Control (IQC), Material Review Board (MRB), and Corrective and Preventive Actions (CAPA). Professional certifications such as ASQ CQE, CQA, CMQ/OE, Lean Six Sigma Black Belt, ISO Lead Auditor, or equivalent quality certifications strongly preferred.
Director_Manufacturing Quality Consultant_ Life Sciences PricewaterhouseCoopers LLPDirector_Manufacturing Quality Consultant_ Life SciencesMA$155,000ā$410,000 / yearDemonstrates some proven abilities to collaborate and work with a diverse team including: Basic problem solving and analysis skills; Financial modeling skills; Basic spreadsheet, presentation and document development skills; Demonstrates the ability to build, maintain, and utilize networks of client relationships; Interpersonal skills and proactive communication; and, Collaborative and "can-do" mindset eager to take on challenges. PwC does not intend to hire experienced or entry level job seekers who will need, now or in the future, PwC sponsorship through the H-1B lottery, except as set forth within the following policy: https://pwc.to/H-1B-Lottery-Policy.
Sr. Director, Supply Chain QA Ultragenyx Pharmaceutical IncSr. Director, Supply Chain QABedford, MA$251,300ā$310,500 / yearThe successful candidate will bring deep hands-on experience with global GDP requirements, temperature controlled supply chains, and complex international distribution networks, and will serve as the quality authority for supply chain operations across internal teams and external partners. Ultragenyx is seeking an experienced Senior Director, Supply Chain Quality to provide global quality leadership and oversight across packaging, labeling, global logistics, distribution, and external supply chain partners supporting both clinical and commercial products.
Associate Director, Head of IMP Quality Takeda Pharmaceutical Co LtdAssociate Director, Head of IMP QualityLexington, MA$153,600ā$241,340 / yearThe 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. Takeda is seeking an experienced Associate Director, Head of IMP Quality to lead quality operations for investigational medicinal products (IMPs) from clinical development through to commercialization.
Director, Quality Control Oruka Therapeutics IncDirector, Quality ControlWaltham, MA$213,000ā$240,000 / yearRole Overview: The 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.
Director of Quality- Grafton and Dillon Precision Castparts CorpDirector of Quality- Grafton and DillonMAp>for description go through this url https://pcctalentacquisitionportal.tal.net/vx/mobile-0/appcentre-ext/brand-7/candidate/so/pm/1/pl/3/opp/22565-Director-of-Quality-Grafton-and-Dillon/en-GB.
Program Director, Knowledge & QA BullhornProgram Director, Knowledge & QAMassachusettsp>The Program Director, Knowledge & QA is a new, high-visibility individual contributor role that will own the design, execution, and continuous improvement of Bullhorn's Knowledge-Centered Service (KCS) program and Global Support Quality Assurance (QA) program. Bullhorn's core purpose is to create an incredible customer experience, and the organization has a sharp focus on delivering very high quality products and services to its customers.Quality Director (24568) Natel Engineering Co. Inc. (Inactive)Quality Director (24568)Westborough, MAp>Benefits Offered: Comprehensive benefit package including medical, dental and vision coverage; company-paid basic life/AD&D insurance, short-term and long-term disability insurance; voluntary supplemental insurances, flexible spending accounts and employee assistance program (EAP). Summary: Manage the quality organization, develop quality policies, generate quality reports and provide support to organizations within the Company on quality-related issues.Director, GMP Quality Assurance Oruka Therapeutics IncDirector, GMP Quality AssuranceWaltham, MA$213,000ā$240,000 / yearReview 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.Director, Pharmacovigilance Quality Assurance Dyne Therapeutics IncDirector, Pharmacovigilance Quality AssuranceWaltham, MA$190,000ā$232,800 / yearThis role leads the design and execution of Dyne's Pharmacovigilance Quality Management System (QMS), including policies, procedures, audits, inspections, inspection readiness, and vendor oversight, to ensure PV systems and processes meet global regulatory requirements and support high-quality regulatory submissions. The company is advancing clinical programs for Duchenne muscular dystrophy (DMD) and myotonic dystrophy type 1 (DM1) as well as a preclinical programs for facioscapulohumeral muscular dystrophy (FSHD) and Pompe disease.Senior Director Quality Assurance Filtration Danaher CorpSenior Director Quality Assurance FiltrationMarlborough, MA$215,000ā$250,000 / yearli>Demonstrated understanding of root cause analysis, corrective and preventive action (CAPA), change control, verification and validation methodologies, manufacturing/production process control methodologies, risk management, and continuous improvement in a medical device environment. What you will do: Partner with the Global QARA leaders and the Filtration leadership to drive functional initiatives, supportive of the business priorities, enabling business strategy and growth.Director, Quality Control TScan Therapeutics IncDirector, Quality ControlWaltham, MA$210,000ā$220,000 / yearThe submission of unsolicited resumes by recruitment or staffing agencies to TScan Therapeutics or its employees is strictly prohibited unless contacted directly by TScan Therapeutics internal Talent Acquisition team. Reporting to the Associate Vice President of QC and AD, the ideal candidate should have relevant experience in compendial, cellular, molecular, and environmental monitoring in a cGMP facility, and enjoy fast-paced, collaborative, and vibrant culture.Assoc. Director, Quality - Commercial Kiniksa Pharmaceuticals International PlcAssoc. Director, Quality - CommercialLexington, MA$186,000ā$200,000 / yearp>The Associate Director, Quality is responsible for providing quality leadership and oversight for all GMP technical transfer activities, including process transfer from development to commercial manufacturing, siteātoāsite transfers, and CMO/CDMO technology transfers. Execute and support GMP quality Systems, including deviations, investigations, CAPA's, change control, batch review, CPV, OOS/OOT management, and stability programs, ensuring timely and compliant closure.Director, Quality Management Systems Dyne Therapeutics IncDirector, Quality Management SystemsWaltham, MA$196,000ā$230,000 / yearThis role is responsible for key elements of the QMS including supplier quality, audits, and product complaint management programs, ensuring these systems are inspection-ready, risk-based, and aligned with global regulatory expectations. Role Summary: The Director, Quality Management Systems is a quality leader responsible for designing, scaling, and advancing a global Quality Management System (QMS) that supports Dyne's transition to commercial operations.Director, Quality Microbiology Integra LifeSciences Holdings CorpDirector, Quality MicrobiologyMA$166,750ā$228,850 / yearp>ESSENTIAL DUTIES AND RESPONSIBILITIES. To perform this job successfully, an individual must be able to perform each essential duty satisfactorily: Provide technical talent training, mentoring, and development support for microbiology personnel and cross-functional teams. The candidate must be an experienced team leader who leverages the talent of their team to increase performance, generate results, and maintain robust quality of manufacturing site microbiology programs.Director, Quality Systems (Remote) Steris PlcDirector, Quality Systems (Remote)Northborough, MARemote$144,500ā$187,000 / yearThe Director, Quality Systems leads teams of Senior Quality Managers, Quality Managers, Analysts/Engineers, and Technicians responsible for product quality, product release, supplier quality, continuous improvement support, technical support/technical guidance, and quality system execution. The Director, Quality Systems is responsible for leading, planning, developing, and directing quality operations policies, programs, initiatives, and overall execution of the STERIS QMS within multiple facilities spread across geographical regions and countries.Director, Clinical Quality TScan TherapeuticsDirector, Clinical QualityWaltham, MA$217,500ā$230,000 / yearli>Quality Assurance Activities:Conduct GCP audits, including investigator sites, clinical vendors, and clinical systems such as trial master files, clinical databases, pharmacovigilance, etc. The ideal candidate will possess deep expertise in quality assurance within clinical research, a strong understanding of the regulatory landscape for cell and gene therapy, and the ability to collaborate effectively across cross-functional teams.Sr. Director, External Manufacturing Quality, Cell Therapy Bristol-Myers Squibb CoSr. Director, External Manufacturing Quality, Cell TherapyMA$238,200ā$288,637 / yearp>To define and shape the Quality strategy for global Contract Manufacturing Organizations (CMO) and associated Contract Test Labs (CTLs) management for the Cell Therapy External Manufacturing (ExM) network and to ensure a high level of cGMP compliance and the safety, efficacy, and quality of externally manufactured commercial products. To build relationships with senior leadership in the CMO and CTL network to support the Virtual Plant Teams (VPTs) and Virtual Analytical Teams (VATs) and to proactively manage and improve CMO Quality performance through risk-based oversight and periodic reviews.12345678910Similar Job SearchesDirector Of Quality JobsDirector Of Quality Management JobsLine Leader JobsMaintenance Worker JobsProduction Manager JobsQuality Assurance JobsQuality Control Manager JobsQuality Coordinator JobsQuality Manager JobsQuality Specialist Jobs
Quality Director (24568) Natel Engineering Co. Inc. (Inactive)Quality Director (24568)Westborough, MAp>Benefits Offered: Comprehensive benefit package including medical, dental and vision coverage; company-paid basic life/AD&D insurance, short-term and long-term disability insurance; voluntary supplemental insurances, flexible spending accounts and employee assistance program (EAP). Summary: Manage the quality organization, develop quality policies, generate quality reports and provide support to organizations within the Company on quality-related issues.
Director, GMP Quality Assurance Oruka Therapeutics IncDirector, GMP Quality AssuranceWaltham, MA$213,000ā$240,000 / yearReview 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.
Director, Pharmacovigilance Quality Assurance Dyne Therapeutics IncDirector, Pharmacovigilance Quality AssuranceWaltham, MA$190,000ā$232,800 / yearThis role leads the design and execution of Dyne's Pharmacovigilance Quality Management System (QMS), including policies, procedures, audits, inspections, inspection readiness, and vendor oversight, to ensure PV systems and processes meet global regulatory requirements and support high-quality regulatory submissions. The company is advancing clinical programs for Duchenne muscular dystrophy (DMD) and myotonic dystrophy type 1 (DM1) as well as a preclinical programs for facioscapulohumeral muscular dystrophy (FSHD) and Pompe disease.
Senior Director Quality Assurance Filtration Danaher CorpSenior Director Quality Assurance FiltrationMarlborough, MA$215,000ā$250,000 / yearli>Demonstrated understanding of root cause analysis, corrective and preventive action (CAPA), change control, verification and validation methodologies, manufacturing/production process control methodologies, risk management, and continuous improvement in a medical device environment. What you will do: Partner with the Global QARA leaders and the Filtration leadership to drive functional initiatives, supportive of the business priorities, enabling business strategy and growth.
Director, Quality Control TScan Therapeutics IncDirector, Quality ControlWaltham, MA$210,000ā$220,000 / yearThe submission of unsolicited resumes by recruitment or staffing agencies to TScan Therapeutics or its employees is strictly prohibited unless contacted directly by TScan Therapeutics internal Talent Acquisition team. Reporting to the Associate Vice President of QC and AD, the ideal candidate should have relevant experience in compendial, cellular, molecular, and environmental monitoring in a cGMP facility, and enjoy fast-paced, collaborative, and vibrant culture.
Assoc. Director, Quality - Commercial Kiniksa Pharmaceuticals International PlcAssoc. Director, Quality - CommercialLexington, MA$186,000ā$200,000 / yearp>The Associate Director, Quality is responsible for providing quality leadership and oversight for all GMP technical transfer activities, including process transfer from development to commercial manufacturing, siteātoāsite transfers, and CMO/CDMO technology transfers. Execute and support GMP quality Systems, including deviations, investigations, CAPA's, change control, batch review, CPV, OOS/OOT management, and stability programs, ensuring timely and compliant closure.
Director, Quality Management Systems Dyne Therapeutics IncDirector, Quality Management SystemsWaltham, MA$196,000ā$230,000 / yearThis role is responsible for key elements of the QMS including supplier quality, audits, and product complaint management programs, ensuring these systems are inspection-ready, risk-based, and aligned with global regulatory expectations. Role Summary: The Director, Quality Management Systems is a quality leader responsible for designing, scaling, and advancing a global Quality Management System (QMS) that supports Dyne's transition to commercial operations.
Director, Quality Microbiology Integra LifeSciences Holdings CorpDirector, Quality MicrobiologyMA$166,750ā$228,850 / yearp>ESSENTIAL DUTIES AND RESPONSIBILITIES. To perform this job successfully, an individual must be able to perform each essential duty satisfactorily: Provide technical talent training, mentoring, and development support for microbiology personnel and cross-functional teams. The candidate must be an experienced team leader who leverages the talent of their team to increase performance, generate results, and maintain robust quality of manufacturing site microbiology programs.
Director, Quality Systems (Remote) Steris PlcDirector, Quality Systems (Remote)Northborough, MARemote$144,500ā$187,000 / yearThe Director, Quality Systems leads teams of Senior Quality Managers, Quality Managers, Analysts/Engineers, and Technicians responsible for product quality, product release, supplier quality, continuous improvement support, technical support/technical guidance, and quality system execution. The Director, Quality Systems is responsible for leading, planning, developing, and directing quality operations policies, programs, initiatives, and overall execution of the STERIS QMS within multiple facilities spread across geographical regions and countries.
Director, Clinical Quality TScan TherapeuticsDirector, Clinical QualityWaltham, MA$217,500ā$230,000 / yearli>Quality Assurance Activities:Conduct GCP audits, including investigator sites, clinical vendors, and clinical systems such as trial master files, clinical databases, pharmacovigilance, etc. The ideal candidate will possess deep expertise in quality assurance within clinical research, a strong understanding of the regulatory landscape for cell and gene therapy, and the ability to collaborate effectively across cross-functional teams.
Sr. Director, External Manufacturing Quality, Cell Therapy Bristol-Myers Squibb CoSr. Director, External Manufacturing Quality, Cell TherapyMA$238,200ā$288,637 / yearp>To define and shape the Quality strategy for global Contract Manufacturing Organizations (CMO) and associated Contract Test Labs (CTLs) management for the Cell Therapy External Manufacturing (ExM) network and to ensure a high level of cGMP compliance and the safety, efficacy, and quality of externally manufactured commercial products. To build relationships with senior leadership in the CMO and CTL network to support the Virtual Plant Teams (VPTs) and Virtual Analytical Teams (VATs) and to proactively manage and improve CMO Quality performance through risk-based oversight and periodic reviews.