Director of Quality and Compliance
$162k - $258kPhilips
Job TitleDirector of Quality and ComplianceJob DescriptionThe Director of Quality & Compliance plays an important leadership role within Philips’ Image Guided Therapy Devices quality organization, focused on Quality system harmonization/simplification, the introduction/implementation of quality processes/tools, FDA/Notified body compliance and effective Management Review processes/reporting.Your role:You will lead, manage and develop the Image Guided Therapy Devices (IGTD) quality systems team, driving an inclusive, supportive environment and strong employee engagement.You’re Responsible for ensuring the effective operation/evolution of the Quality Management System (QMS), ensuring the QMS is compliant with the applicable regulatory requirements, industry standards and internal policies (inclusive of compliance of PDLM and manufacturing processes and execution of change management, internal /external audit process, CAPA process, and management of Quality system KPIs and objectives).You will act as advisor to senior leadership on all quality related matters, formulating/implementing the Business’ strategic vision for QMS programs aligned with the business objectives (long-range quality, regulatory and compliance policy), ensuring that quality systems support the organization’s goals.You will be responsible for enforcing the simplification/harmonization of quality systems across the Business sites/sector; establish an effective Management Review process, routine reporting and introduce/implement the quality processes/ tools required to ensure product quality and customer satisfaction.You will act as the quality representative on the Business Category Leadership Team, providing strategic quality leadership and partnering cross-functionally to shape and execute category strategy, proactively resolve business and quality challenges, drive operational excellence, and ensure quality objectives are integrated into key business decisions.You're the right fit if:You’ve acquired a minimum of 10+ years' experience in global, FDA regulated medical device environments, including proven functional and strategic leadership of diverse quality teams in various aspects of Quality, including, quality systems/QMS implementation, simplification, standardization, CAPA, Change Management and internal/external audit for multi-site businesses in a large, multi-national, global/matrix organization (s).You’re experienced in utilizing, monitoring KPI’s to assess the performance of the team and QMS to drive high performance/process improvement and well versed in business process management frameworks, including industry best practices related to FDA regulated QMS.You have proven expertise/knowledge of global medical device regulations, requirements, and standards, such as FDA, ISO13485, ISO14971, EUMDR for all classifications of medical devices.You are a highly collaborative, strategic leader, influencer, with strong experience in change management and ability to effectively communicate/build relationships with internal/external stakeholders and at all levels of the organizationYou have a minimum of a Bachelor's degree in Quality, Life Sciences, Engineering or similar technical discipline-REQUIRED, Master's degree in business, management or quality, strongly preferred.You must be able to successfully perform the following minimum Physical, Cognitive and Environmental job requirements with or without accommodation for this position. How we work together:We believe that we are better together than a part. For our office-based teams, this means working in-person at least 3 days per week. Onsite roles require full-time presence in the company’s facilities. Field roles are most effectively done outside of the company’s main facilities, generally at the customers’ or suppliers’ locations. This is an Office-Based role.About Philips:We are a health technology company. We built our entire company around the belief that every human matters, and we won't stop until everybody, everywhere, has access to the quality of healthcare that we all deserve. Do the work of your life to help improve the lives of others.Learn more about our business.Discover our rich and exciting history.Learn more about our purpose.Learn more about our culture.Philips Transparency Details:The pay range for this position in Colorado Springs, CO is $162,000 to $258,000.The pay range for this position in Plymouth, MN is $170,000 to $270,000.The pay range for this position in San Diego, CA is $181,000 to $288,000.At Philips, it is not typical for an individual to be hired at or near the top end of the range for their role and compensation decisions are dependent upon the facts and circumstances of each case. The actual base pay offered may vary within the posted ranges depending on multiple factors including job-related knowledge/skills, experience, business needs, geographical location, and internal equity. In addition, other compensation, such as an annual incentive bonus, sales commission or long-term incentives may be offered. Employees are eligible to participate in our comprehensive Philips Total Rewards benefits program, which includes a generous PTO, 401k (up to 7% match), HSA (with company contribution), stock purchase plan, education reimbursement and much more. Details about our benefits can be found here. Additional InformationUS work authorization is a precondition of employment. The company will not consider candidates who require sponsorship for a work-authorized visa, now or in the future.Company relocation benefits will not be provided for this position. For this position, you must reside in or within commuting distance to Colorado Springs, CO, Plymouth, MN or San Diego, CA.This role may require travel up to 10%#LI-PH1This requisition is expected to stay active for 45 days but may close earlier if a successful candidate is selected or business necessity dictates. Interested candidates are encouraged to apply as soon as possible to ensure consideration.Philips is an Equal Employment and Opportunity Employer including Disability/Vets and maintains a drug-free workplace.Job SummaryJob number: 587271Date posted : 2026-07-17Profession: Quality & RegulatoryEmployment type: Full time
$270k - $290k
...transformative therapies.For more information, visit .Job Summary: The Executive Director, GMP Quality Assurance leads Artiva Biotherapeutics’ internal GMP quality operations and compliance program, ensuring that cell therapy products manufactured and tested for...SuggestedFlexible hours$181k - $288k
Job TitleDirector, Quality & Regulatory- Mergers & Acquisitions (M&A)Job DescriptionThe Director, Quality & Regulatory M&A is an enterprise Q&R leader for M&A activities... ...strategies, ensuring continuity of compliance and regulatory obligations from due diligence...SuggestedFull timeWork at officeImmediate startWork visaRelocation package3 days per week$120k - $145k
...bring new therapies to patients in need. The PositionThe Clinical Quality System Document Manager is responsible for the management,... ...Assurance to ensure document consistency, harmonization, and compliance across functional areas. The incumbent will contribute to the...SuggestedContract workWork at office$150k - $172k
...collaborating closely with all development functional areas to embed quality into every stage of the program.Essential Duties &... ...oversight across all phases of clinical development to ensure compliance with ICH-GCP, applicable regulations, and Artiva’s procedures....SuggestedContract workFlexible hours- As a Quality Programs Manager 4, you will be a key leader responsible for ensuring regulatory compliance, driving continuous improvement, and embedding industry best practices across our Quality Management System (QMS). You will lead and manage cross-functional quality...Suggested
- ...seeking a seasoned FSQA Manager to lead the QA department, ensuring compliance with company policies and regulatory standards across the... ...staff and driving continuous improvement in food safety, quality, and regulatory readiness for audits and customers. This role...
$125k - $140k
...QUALITY MANAGER At Lighteum, we pride ourselves on being more than just a place of work... ...(QMS) for the San Diego site, ensuring compliance with regulatory, customer, and business... ...SCOPE The incumbent reports to the Quality Director and is responsible for the overall leadership...Work at officeWorldwideFlexible hours$100k - $130k
...We are looking for an experienced Quality Manager to ensure that our products and services meet all necessary requirements before they... ...inspect the final product to make sure it has been built with compliance to legal standards and meets customer expectations. A great...- ...For more information, visit . Position Summary The Senior Director, Quality (SD) is responsible for all aspects of the quality organization... ...impact product integrity, patient safety, regulatory compliance, and business continuing. The SD works with both internal and...Temporary workWork at office
$189k - $246k
...common goal of elevating science and service for rare patients.Position Summary:The Director, Quality Assurance - Technical is responsible for providing technical quality and compliance support and/or oversight of the contract manufacturing, testing, storage and distribution...Full timeContract workTemporary workWork experience placementRemote workShift work- ...and qualified individual to join our team as an Associate Director, Clinical Quality Assurance. This role provides strategic and operational leadership... ...the highest standards of Good Clinical Practice (GCP) compliance across all clinical programs. This role is responsible for...Full timeTemporary workLocal areaMonday to Friday
$134k - $186k
...and improvement opportunities, and lead cross-functional teams in developing and implementing effective solutions to enhance quality and compliance.• Serves as a senior quality advisor and key point of contact for regulatory bodies, ensuring that QMS processes and...Full timeWork at officeImmediate startRemote workWork visaRelocation package3 days per week$150k - $195k
...elevating science and service for rare patients.Position Summary:The Associate Director, Quality Assurance - Technical, is responsible for leading and providing GxP Analytical quality/compliance support and/or oversight as per requirements and applicable guidance. This...Full timeContract workTemporary workInterim roleRemote work$180k - $230k
...innovators who are collaborating to bring new therapies to patients in need. The Position The Associate Director/ Director of Drug Safety & Pharmacovigilance (PV) Quality & Compliance, is a key role and is responsible for oversight of Drug Safety & PV quality, compliance, and...$130k - $170k
...0/yr - $170,000.00/yr Salary Range: $135,000 - $170,000 The Quality & Continuous Improvement Manager is responsible for ensuring that... .... Review and update quality manual periodically for compliance to prevailing ISO and customer requirements and specifications...Full timeAll shifts$110k - $135k
...potentially transformative therapies.For more information, visit.Job Summary:Artiva Biotherapeutics is seeking a skilled and motivated Quality Control Supervisor who will be reporting to the Senior Manager, Quality Control. This individual will supervise the Bio Team and...Flexible hours$175k - $215k
San Diego, CACapricor Therapeutics - Quality Assurance /Full-time (exempt) /On-siteCapricor... ...and families who need them most.The Director, Quality Assurance & Quality Systems will... ...management strategies and systems to ensure compliance with GMP, FDA, ICH guidelines, and other...Full timeWork at office- ...future of science, we’re in. Are you?About the Role:The Senior Director Quality Assurance will lead Gene Therapy QA oversight for product... ...and commercialization. You will ensure phase-appropriate GMP compliance across manufacturing development, while providing strategic...Full timeContract workWork experience placementWork at officeLocal areaFlexible hours3 days per week
- ...The Director of Quality and Risk Management is responsible for the strategic planning, implementation, oversight, and continuous improvement... ...Management Program, Patient Safety Program, and Regulatory Compliance activities. This position promotes a culture of safety,...Temporary workFor contractors
$120.55k - $186.85k
...patient experiences through innovative, integrated care. The RN Director focuses on population health management, including preventive... ...disparities and optimize resource utilization. They lead quality improvement initiatives, such as clinical process enhancements...Local area- JOB DESCRIPTION Job Summary Provides subject matter expertise and leadership for Medicare Stars quality improvement (QI) programs and activities. Provides subject matter expertise in planning and implementing QI initiatives and education programs to support improved Medicare...Work at officeRemote work
$167k - $216k
...That includes you. We are not only investing in what’s next in construction, we are investing in what’s next for your career.As a Quality Manager - Construction for PCL Construction, Inc. in San Diego, California, you’ll have the opportunity to lead and uphold the construction...Contract workFor contractors$78.64k - $117.96k
...your skills toward causes you care about—locally and globally. Come make an impact every day at Zebra. What We’re Looking For The Quality Supervisor is responsible for planning, organizing, leading and controlling the Operational Quality function relating to the assurance...Work experience placementSummer workLocal areaFlexible hours- ...a trusted partner, Veridiam provides technical collaboration, quality assurance, and supply chain reliability essential to advancing... ...operations, ensuring work is performed safely, efficiently, and in compliance with applicable codes, standards and customer requirements....Permanent employment
- ...Overview Testing software that saves lives. About the Role Join the Quality Management team at Epic and become the last line of defense for software that impacts the lives of 305 million people worldwide. As a Quality Manager, you’ll collaborate closely with developers...WorldwideRelocationVisa sponsorship
- ...The Quality Manager leads the end-to-end quality system for a Private Label company ensuring products meet consumer safety, regulatory, and brand standards across various beauty categories. This role owns quality KPIs, incident reporting and escalation, traceability, supplier...Contract workWork at officeRemote workMonday to Friday
$142k - $168k
...the Role Firestorm Labs is seeking a proactive and strategic Quality Manager to join our growing team in San Diego. The Site Quality... ...support operational efficiency, early production builds, and future compliance needs. You will also be responsible for building the site’s...Permanent employmentTemporary workWork at officeLocal areaRelocationRelocation package$124k - $161k
...Manager, Quality Control At Insmed, every moment and every patient counts — and so does every person who joins in. As a global biopharmaceutical... ...for patients with serious diseases. Reporting to the Associate Director, Quality Control, you'll be responsible for overseeing and...Full timeWork at officeFlexible hours$125k - $132k
...Quality Manager – Lead Quality Excellence in a High-Profile 24/7 Warehouse Start-Up! Salary Range: $125,000 to $132,000 Annually... ...on accuracy, efficiency, and customer satisfaction Ensure compliance with customer requirements, operational standards, and company...Contract workWork experience placementLocal areaAll shiftsShift work$100k - $120k
...Quality Supervisor AXILLON AEROSPACE is a leading provider of complex, highly engineered composite and polymer solutions for demanding... ...forth by quality assurance, or engineering function. Ensure compliance to Axillon Aerospace Standard Procedures and Work Instructions...Permanent employmentFull timeWork experience placement
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