Director OF Quality
$229k - $280kKailera Therapeutics
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. Rooted in an entrepreneurial spirit and a team-oriented culture, we are working together to advance Kailera’s mission to advance novel therapies for obesity and related conditions. We are passionate about creating an inclusive workplace that promotes collaboration, integrity, and excellence. As we expand, we seek the most talented individuals with diverse backgrounds, cultures, perspectives, and experiences to join our team. What You’ll Do: 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). You will report to the Vice President, Quality and will serve as the primary architect of our quality framework, ensuring our global operations remain compliant with GxP standards while maintaining the agility required of a growing biotech. Required location: Waltham, MA (hub-based, onsite 3-4 days per week) Responsibilities: Define and execute the long-term vision for the Quality Management System (QMS) to support global clinical development and future commercialization Provide Quality oversight for GxP systems change controls. Support validation planning, execution, approvals Act as the Business Owner for Veeva QualityVault. Lead the optimization of modules including Document Control, Training, Deviations, CAPA, and Change Control Establish and lead Quality Management Reviews (QMR). Develop and report on Key Quality Indicators (KQIs) and metrics to senior leadership to drive proactive risk management Ensure the QMS meets global regulatory requirements (FDA 21 CFR Parts 11, 210, 211, and 820; ICH E6; EudraLex Volume 4) Lead the QMS strategy for inspection readiness. Serve as a key interface during regulatory inspections (FDA, EMA, etc.) and oversee the internal and vendor audit programs Champion a culture of Quality. Streamline complex workflows to reduce cycle times for document approvals and deviation closures without compromising compliance Build and mentor a high-performing team of Quality professionals, fostering a collaborative environment that balances technical rigor with pragmatic problem-solving Required Qualifications: 12+ years of experience in Quality Assurance within the Biotech/Pharmaceutical industry, with at least 5 years in a senior leadership capacity Direct experience implementing or managing Veeva QualityVault is mandatory. You should be proficient in configuring workflows and leveraging the platform for data‑driven decision‑making Proven track record in mid‑sized companies navigating the transition from early‑phase clinical trials to late‑stage pivotal studies Deep knowledge of global GxP regulations and experience participating in (or leading) successful regulatory inspections Exceptional ability to translate complex quality requirements into actionable business strategies for non‑quality stakeholders Education: Bachelor’s degree required, scientific or engineering discipline preferred Advanced degree preferred Salary Range $229,000–$280,000 USD For Full Time Roles: This range represents the company’s good‑faith estimate of the salary at the time of posting. Actual pay may vary based on experience, skills, qualifications, location, and internal equity. We also offer comprehensive health coverage, flexible time off, paid holidays, and a year‑end shutdown. Enjoy a monthly wellness stipend, generous 401(k) match, tuition reimbursement, commuter benefits, disability and life insurance, plus annual bonus opportunities and equity grants—because your well‑being and future matter to us. EQUAL EMPLOYMENT OPPORTUNITY INFORMATION: Kailera Therapeutics, Inc. is an Equal Opportunity Employer that does not discriminate on the basis of actual or perceived race (including traits historically associated with race, such as hair texture and protective hairstyles), color, creed, religion (including religious dress and grooming practices), national origin, ancestry, citizenship status, age (40 and over), sex or gender (including pregnancy, childbirth, pregnancy‑related conditions, and lactation), gender identity or expression (including transgender status), sexual orientation, marital status, military service and veteran status, physical or mental disability, genetic information, reproductive health decisions, domestic victim status, political affiliation, or any other characteristic protected by applicable federal, state, or local laws and ordinances. E-Verify: Kailera uses E-Verify to confirm the identity and employment eligibility of all new hires. #J-18808-Ljbffr
- ...About the role. 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...Suggested
$146k - $196k
...autonomy, AI, computer vision, sensor fusion, and networking technology to the military in months, not years. ABOUT THE TEAM: Our Quality Engineering team is a dedicated group of professionals committed to ensuring the highest standards of quality in our processes. We...SuggestedFull timeWork experience placementImmediate startRelocation$232k - $285k
...Soufflé Therapeutics | Head of Quality Control | Job Description Soufflé Therapeutics is a biotech company focusing on the cell-type... ...where testing, development, and manufacturing are outsourced, the Director establishes governance with CDMOs/CROs, oversees analytical...SuggestedWork at office$213.6k - $320.4k
...Job Description The Senior Director, Global Quality Systems holds a pivotal leadership position within the Quality organization. This individual is responsible for providing strategic vision and direction to advance the framework, strengthen organizational capabilities...SuggestedContract workWork experience placementSummer workRemote workFlexible hours2 days per week- ...Zevra Therapeutics, Inc. is seeking a Director of Quality Assurance (Operations) to lead the Quality Management System and ensure compliant development and commercial operations. The role emphasizes building scalable processes, cross‑functional collaboration, and oversight...SuggestedRemote work
- ...The Director of Quality is responsible for overseeing all quality assurance efforts, including the development and implementation of a quality assurance program. Essential duties & responsibilities Serve as the primary liaison across internal teams and external partners...Work at officeLocal area
$168.75k - $257.8k
...Director of Quality Catalent, Inc. is a leading global contract development and manufacturing organization (CDMO) whose mission is to develop, manufacture, and supply products that help people live better and healthier lives. Catalent is dedicated to delivering unparalleled...Contract workLocal area$168.75k - $257.8k
...pharma, biotech, and consumer health customers, supporting product development, launch, and full life‑cycle supply. The Role Ensure the Quality function complies with Health, Safety and Environmental requirements and employees adhere to the “Standards of Business Conduct.”...Contract workLocal area$95k - $120k
...We are currently searching for an experienced Quality Manager for a well-established company. The ideal candidate will be responsible for managing the day-to-day manufacturing, production, logistics, and overall business operations. Quality Manager Responsibilities...Contract workShift work- ...re at an inflection point, moving from development through FDA submission, manufacturing ramp, and product launch. We need a Director of Quality who has been here before: someone who can hold the rigor of a regulated medical device environment without killing the speed...Day shift
- ...Quality Manager Integrated Resources, Inc is a premier staffing firm recognized as one of the tri-states most well-respected professional specialty firms. IRI has built its reputation on excellent service and integrity since its inception in 1996. Our mission centers...Immediate start
- General Job Description: Position will include but not limited to, supervise and schedule department as work load requires. Maintains supervision within department to ensure timely processing of various jobs. Set-up and the use of inspection equipment, in-process ...Work experience placement
- ...long‑lasting partnerships with our members, our providers, and you! Role Overview Reporting to the CMO of eternalHealth, the Director of Quality is responsible for the design, implementation, monitoring, and continuous improvement of the eternalHealth Quality Management...
- ...Hybrid - 3 days onsite / 2 days remote Reports to: CEO | Team: Quality About PhAST PhAST develops leading technology for microbiology... ...system to support it. Job Description PhAST is seeking its Director of Quality to own the company's Quality Management System (QMS)...Full timeContract workImmediate startRemote work
$85k - $110k
...under federal and state contracts, including work with the EPA and other government clients in the areas of drinking water, water quality, and resilience. In this role, you will lead the planning, execution, and delivery of complex task orders, ensuring alignment with...Permanent employmentContract workWork experience placementLocal areaWorldwide- ...Director, Quality Control (QC) Location: Cambridge, MA (Hybrid) Overview An innovative biotechnology company developing next-generation biologics and engineered fusion protein therapeutics focused on immune and autoimmune-driven diseases is seeking a Director of Quality...
$191k - $253k
...military in months, not years. ABOUT THE JOB We are seeking a Director of Supply Chain to lead procurement, supply planning,... ...will be asked to lead cross-functional projects to achieve cost, quality, and delivery targets. As a member of the Supply Chain team,...Full timeWork experience placementImmediate start- ...Dyne Therapeutics, based in Waltham, MA, seeks an Associate Director, Quality Management Systems to design and scale a global QMS for commercial operations. You will own document control, records management, and training, ensuring systems are inspection-ready and aligned...
$140k - $200k
...estimates. You will also ensure that project teams are appropriately staffed with the technical expertise necessary to deliver high-quality results while maintaining cost efficiency. Additional responsibilities include serving as the primary point of contact for...Immediate start- ...schedules, define scopes of work, and develop cost estimates. Staff project teams with adequate technical expertise to deliver high‑quality results while maintaining cost efficiency. Act as the primary point of contact for assigned clients, providing regular updates,...Immediate start
$138k - $190k
...Job Description The Senior Manager, Clinical Quality Assurance is responsible for the development, maintenance and oversight of GCP activities related to the Clinical Trial activities sponsored by Deciphera. The primary responsibilities are to ensure both quality and compliance...Contract work$160k - $195k
...individuals, families and communities. Learn more at , and follow us on X, LinkedIn and Facebook. Role Summary The Associate Director, Quality Management Systems is a key member of the quality team responsible for designing, scaling, and advancing a global Quality Management...Local area$120k - $145k
...Water Resources Project Manager to join its dynamic team of Water Resource scientists and engineers and support our growing water quality and stormwater regulatory planning and compliance work. This is an exciting opportunity to work with a cutting edge, innovative team...Full timeLocal areaFlexible hours- ZoomInfo is seeking an AI‑forward Learning & Development Manager III to lead scalable learning experiences, onboarding, and capability building. This role blends hands‑on execution with systemic improvements across learning technology, operations, and analytics. Ideal ...
$84k - $132k
...optimization, and delivery across learning technology, onboarding, capability-building, and learning operations. Reporting to the Director, Learning & Development, this role will help bring L&D strategy to life through strong program execution, systems administration,...Worldwide$155k - $190k
...biotechnology company located in Waltham is seeking an Associate Director, Trial Master File (TMF) Lead. This role involves developing... ...compliance with regulatory requirements, and overseeing documentation quality. The ideal candidate will possess over 8 years of experience in...- ...job poster from Real Time Recruitment Solutions (RTRS) Hiring: Quality Manager – Specialized Manufacturing We’re looking for an experienced... ...Boston, MA $132,900.00-$199,400.00 4 days ago Sr Mgr/Associate Director, GMP Quality Assurance Wilmington, MA $65,000.00-$80,000.00 16...16 hoursFull time
- ...Quality Manager Responsible for collaborating with internal business partners to review and solidify quality systems and quality metrics, while identifying specific areas of opportunity to provide world class service to customers. Identify gaps in quality processes,...Work experience placementWork at office
- ...customer project teams to help them realize their goals, whether an accelerated time to market, efficient scale-up, a consistent, quality supply, or any combination thereof. Their experienced teams are focused specifically on serving the medical markets and delivering...Work at officeFlexible hours
$182.35k - $228.01k
...Quality Manager This is an exciting job opportunity for you as a Quality Manager in Burlington, Massachusetts with Signify to formulate and implement the business' long-term quality, regulatory, and compliance policy. Key Responsibilities: ~ Enforce compliance...Hourly payFlexible hours
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