Sign up to access all features of our service.
  • Job search
  • Favorites
  • Create a CV
    New
  • Salaries
  • Subscriptions

Senior Manager, Quality Assurance

$157.59k - $203.94k

Gilead

At Gilead, we’re creating a healthier world for all people. For more than 35 years, we’ve tackled diseases such as HIV, viral hepatitis, COVID-19 and cancer – working relentlessly to develop therapies that help improve lives and to ensure access to these therapies across the globe. We continue to fight against the world’s biggest health challenges, and our mission requires collaboration, determination and a relentless drive to make a difference.Every member of Gilead’s team plays a critical role in the discovery and development of life-changing scientific innovations. Our employees are our greatest asset as we work to achieve our bold ambitions, and we’re looking for the next wave of passionate and ambitious people ready to make a direct impact.We believe every employee deserves a great leader. People Leaders are the cornerstone to the employee experience at Gilead and Kite. As a people leader now or in the future, you are the key driver in evolving our culture and creating an environment where every employee feels included, developed and empowered to fulfil their aspirations. Join Gilead and help create possible, together.Job DescriptionAtGileadour pursuit of a healthier world for all people has yielded a cure for hepatitis C, revolutionary improvements in HIV treatment and prevention as well as advancements in therapies for viral and inflammatory diseases and certain cancers.We set and achieve bold ambitions in our fight against the world’s most devastating diseases, united in our commitment to confronting the largest public health challenges of our day and improving the lives of patients for generations to come. As aSenior Manager, Quality Assurance at Gilead you will report to the Associate Director, Quality Assurance within the PDM External Quality organization. This position is dedicated to managing and supporting the Gilead Global Quality Agreement Program.This position will have high visibility throughout the PDM organization as the Global Process Owner (GPO) for Gilead’s Global Quality Agreement Program and will collaborate with key internal partners & stakeholders to establish and maintain an effective Global Quality Agreement Program. This position will serve as the primary subject matter expert (SME) for matters related to Quality Agreement content, Quality Agreement lifecycle management, Quality Agreement negotiations, management of Quality Agreement templates in compliance with applicable laws and regulatory requirements, and supporting continuous improvement initiatives related to the Global Quality Agreement Program.Job ResponsibilitiesServes as the Global Process Owner (GPO) for Gilead’s Global Quality Agreement Program, ensuring the program is compliant, consistent, and effectively implemented across the organizationDevelops, maintains, and continuously improves standardized Quality Agreement templates, guidance documents, training materials, and related tools to align with global regulatory requirements and internal policiesServes as the primary subject matter expert (SME) for Quality Agreement content, interpretation, and applicability across internal teams and external partners, which may include supporting internal stakeholders during review, negotiation, implementation, enforcement, and periodic review of Quality Agreements.Drives alignment and resolution of complex Quality Agreement terms through collaboration with Legal, Sourcing, and External Quality stakeholdersEstablishes and maintains governance processes, metrics, and reporting for the Global Quality Agreement Program to ensure transparency and effectivenessMonitors regulatory trends and evolving expectations related to Quality Agreements and proactively updates program requirements and templates accordinglyProvides expert support during inspections and audits related to Quality Agreements, including preparation, defense, and remediation activitiesLeads or contributes to continuous improvement initiatives to enhance Quality Agreement processes, reduce cycle times, and improve compliance and user experienceSupports training and knowledge-sharing activities to ensure consistent understanding and application of Quality Agreement requirements across the organizationThe best candidate...Demonstrates expertise in Quality Agreements, including development, negotiation, lifecycle management, and governance in a global GMP environmentDemonstrates strong working knowledge of global regulatory requirements applicable to Quality Agreements (e.g., FDA, EMA, ICH) and ability to translate requirements into compliant contract contentDemonstrates strong technical writing skills with the ability to draft, review, and standardize Quality Agreement templates and supporting documentationDemonstrates advanced stakeholder management, influencing, and negotiation skills across cross-functional and external partner environmentsDemonstrates ability to manage and support complex, high-visibility programs with multiple concurrent deliverables and competing prioritiesDemonstrates strong communication skills, including the ability to clearly articulate Quality Agreement expectations to internal stakeholders and external partnersDemonstrates the ability to learn quickly and operate effectively in a fast-paced, highly regulated environmentRequirements8+ years of relevant experience in a GMP environment related field and a BS or BA OR6+ years of relevant experience in a GMP environment related field and a MA/MS OR2+ years of relevant experience in a GMP environment related field and a PhD/PharmDPreferred KnowledgeExperience working with and managing relationships with Contract Manufacturing Organizations (CMOs) and other external partners is preferredExperience interacting with regulatory authorities and supporting inspections related to Quality Agreements or external quality oversight is beneficial and preferredExperience managing global programs or serving as a Global Process Owner (GPO) is beneficialFamiliarity with digital tools or systems supporting document management, contract lifecycle management, or Quality Agreement tracking is beneficialExperience and working knowledge with digital Quality Management Systems and Quality Document Management Systems, particularly Veeva Vault, is beneficial..People Leader AccountabilitiesCreate Inclusion -knowingthe business value of diverse teams, modeling inclusion, and embedding the value of diversity in the way they manage their teams.Develop Talent - understand the skills, experience, aspirations and potential of their employees and coach them on current performance and future potential. They ensure employeesare receivingthe feedback and insight needed to grow,developand realize their purpose.Empower Teams - connect the team to the organization by aligning goals, purpose, and organizationalobjectives, and holding them to account. They provide the support needed to remove barriers and connect their team to the broader ecosystem.The salary range for this position is: $157,590.00 - $203,940.00. Gilead considers a variety of factors when determining base compensation, including experience, qualifications, and geographic location. These considerations mean actual compensation will vary. This position may also be eligible for a discretionary annual bonus, discretionary stock-based long-term incentives (eligibility may vary based on role), paid time off, and a benefits package. Benefits include company-sponsored medical, dental, vision, and life insurance plans*.For additional benefits information, visit: * Eligible employees may participate in benefit plans, subject to the terms and conditions of the applicable plans.For jobs in the United States:Gilead Sciences Inc. is committed to providing equal employment opportunities to all employees and applicants for employment, and is dedicated to fostering an inclusive work environment comprised of diverse perspectives, backgrounds, and experiences. Employment decisions regarding recruitment and selection will be made without discrimination based on race, color, religion, national origin, sex, age, sexual orientation, physical or mental disability,genetic information or characteristic, gender identity and expression, veteran status, or other non-job related characteristics or other prohibited grounds specified in applicable federal, state and local laws. In order to ensure reasonable accommodation for individuals protected by Section 503 of the Rehabilitation Act of 1973, the Vietnam Era Veterans' Readjustment Act of 1974, and Title I of the Americans with Disabilities Act of 1990, applicants who require accommodation in the job application process may contact View email address on click.appcast.io assistance.For more information about equal employment opportunity protections, please view the'Know Your Rights' poster.NOTICE: EMPLOYEE POLYGRAPH PROTECTION ACTYOUR RIGHTS UNDER THE FAMILY AND MEDICAL LEAVE ACTGilead Sciences will not discharge or in any other manner discriminate against employees or applicants because they have inquired about, discussed, or disclosed their own pay or the pay of another employee or applicant. However, employees who have access to the compensation information of other employees or applicants as a part of their essential job functions cannot disclose the pay of other employees or applicants to individuals who do not otherwise have access to compensation information, unless the disclosure is (a) in response to a formal complaint or charge, (b) in furtherance of an investigation, proceeding, hearing, or action, including an investigation conducted by the employer, (c) consistent with the legal duty to furnish information; or (d) otherwise protected by law.Our environment respects individual differences and recognizes each employee as an integral member of our company. Our workforce reflects these values and celebrates the individuals who make up our growing team.Gilead provides a work environment free of harassment and prohibited conduct. We promote and support individual differences and diversity of thoughts and opinion.For Current Gilead Employees and Contractors:Please apply via the Internal Career Opportunities portal in Workday.SummaryLocation: United States - California - Foster CityType: Full time

Vacancy posted 5 days ago
Similar jobs that could be interesting for youBased on the Senior Manager, Quality Assurance in San Mateo, CA vacancy
  • $157.59k - $203.94k

     ...confronting the largest public health challenges of our day and improving the lives of patients for generations to come.  As a Senior Manager, Quality Assurance at Gilead you will report to the Associate Director, Quality Assurance within the PDM External Quality organization.... 
    Senior
    Full time
    Contract work
    For contractors
    Local area

    GILEAD Sciences

    San Mateo, CA
    6 days ago
  • $157.59k - $203.94k

     ...Sr. Manager, Quality Assurance At Gilead, we're creating a healthier world for all people. For more than 35 years, we've tackled diseases such as HIV, viral hepatitis, COVID-19 and cancer – working relentlessly to develop therapies that help improve lives and to ensure... 
    Senior
    Contract work

    GILEAD

    San Mateo, CA
    5 days ago
  • $157.59k - $203.94k

     ...the largest public health challenges of our day and improving the lives of patients for generations to come. As the Sr. Manager, Quality Assurance, you will hold a key role accountable for strategizing and delivering Quality Assurance objectives supporting the Foster... 
    Senior
    Contract work
    For contractors
    Local area

    Gilead Sciences

    Foster, CA
    3 days ago
  • $280k - $300k

     ...our values: care, be real, get it done, and have fun, seriously.POSITION SUMMARYThe Director, GMP Quality Assurance is responsible for the global oversight and management of GMP Quality Assurance operations supporting development and commercial programs.The role manages... 
    Senior
    Contract work
    Local area

    Mirum Pharmaceuticals

    Foster, CA
    2 days ago
  • $164k - $205k

     ...standard of rigor—all in service of patients.The Opportunity:Revolution Medicines is seeking a Senior Manager, Quality Validation who will play a key role within Quality Assurance, providing quality oversight and operational leadership for validation activities across... 
    Senior
    Full time
    Work at office
    Local area
    Worldwide

    Revolution Medicines

    Redwood City, CA
    2 days ago
  •  ...Description As the Senior Director, Quality, you will serve as the quality authority for Sagimet Biosciences, leading and building the company's Quality Management System (QMS) and providing oversight of all Manufacturing Quality activities across the clinical and... 
    Senior

    Sagimet Biosciences Inc.

    Foster, CA
    1 day ago
  • $163k - $191k

     ...equality and clarity across communications and decision making.Summary:We are seeking a dedicated and experienced Senior Manager, Clinical Quality Assurance, to join our dynamic team. The ideal candidate will have a strong background in quality management within a... 
    Senior
    3 days per week

    Vaxcyte

    San Carlos, CA
    3 days ago
  • $173.43k - $204.03k

     ...patients face today. Corcept is headquartered in Redwood City, California. To learn more, visit The Senior Manager of Clinical Quality Assurance (CQA) is a key member of the CQA team and will perform day-to-day clinical quality operations and compliance... 
    Senior
    Full time
    3 days per week

    Corcept Therapeutics

    Redwood City, CA
    3 days ago
  •  ...Sagimet Biosciences is seeking a Senior Director of Quality to lead and scale the company's QMS across clinical and commercial programs. You will...  .... You will drive phase-appropriate risk management, manage audits and inspections, and guide IND/ NDA/ BLA submissions... 
    Senior

    Jobleads-US

    Foster, CA
    2 days ago
  • Nurix Therapeutics in Brisbane, CA is seeking a Senior Manager, electronic Quality Management System (eQMS) to drive quality systems across the development and commercialization lifecycle. You will oversee Deviations, Investigations, CAPAs, Change Controls, Complaints,... 
    Senior

    Nurix Therapeutics

    Brisbane, CA
    2 days ago
  •  ...Google LLC in Mountain View, CA is seeking a Staff AI/ML Product Manager for YouTube Shorts Feed Quality to lead cross-functional teams from concept to launch and refine algorithms delivering engaging short-form videos. You will define ML quality programs, own product... 
    Senior

    Jobleads-US

    San Bruno, CA
    5 days ago
  • $15k

     ...works best for you. Upstart's Product Quality team is responsible for answering a critical...  ...with regulatory requirements. As the Senior Manager, Product Quality at Upstart, you will...  ...and operating quality control or quality assurance programs focused on product, system,... 
    Senior
    Summer work
    Currently hiring
    Local area
    Remote work
    Work from home

    UpStart

    San Mateo, CA
    3 days ago
  • $158.7k - $172.1k

     ...Senior Manager electronic Quality Management System (eQMS) Nurix Therapeutics is a clinical stage biopharmaceutical company focused on the discovery...  ...industry including 4 years in Quality Systems / Quality Assurance. Strong working knowledge of quality system data... 
    Senior
    Full time
    Work at office

    Nurix

    Brisbane, CA
    11 days ago
  • $198k - $242k

     ...abundance for all. About the Team The Quality Engineering team enables 1X to scale...  ...Develop and improve practical Quality Management Systems and MRB processes that establish...  ...Supply Chain, Software, Operations, and senior leadership. Strong operational judgment... 
    Senior
    Temporary work
    Local area
    Flexible hours

    1X

    San Carlos, CA
    1 day ago
  •  ...rigor—all in service of patients. The Opportunity: Revolution Medicines is seeking a Senior Manager, Quality Validation who will play a key role within Quality Assurance, providing quality oversight and operational leadership for validation activities across... 
    Senior
    Full time
    Work at office
    Worldwide

    Revolution Medicines

    Redwood City, CA
    2 days ago
  • $157.59k - $203.94k

     ...Gilead Sciences seeks a Senior Manager of Quality Assurance for its Foster City manufacturing facility. This site-based role drives quality strategy and oversight across GMP operations, regulatory compliance, and product release, supporting facility startup and steady-... 
    Senior
    Contract work

    Gilead Sciences

    Foster, CA
    2 days ago
  • $157.59k - $203.94k

     ...Responsibilities Serve as global process owner for quality agreement program, ensuring compliance and consistent implementation...  ...Expertise in quality agreement development, negotiation, lifecycle management, and governance ~ Strong knowledge of global regulatory... 
    Senior
    Contract work

    Gilead Sciences

    Foster, CA
    a month ago
  • $230k - $260k

     ...The Role We are seeking a highly technical and strategic Senior Product Manager with deep AI/ML expertise to lead development across our agentic...  ...delivering product experiences that improve the speed, quality, and scalability of data operations. You will work closely... 
    Senior
    Temporary work
    Local area

    Snorkel AI

    Redwood City, CA
    15 hours ago
  • $213k - $295k

    Foster City, CAProgram Management Office - PMO /Full-time /HybridThe Program Management Office (PMO) at Zoox is responsible for driving...  ...with upstream teams (e.g. Autonomy, Systems Design & Mission Assurance, Places & Build) and downstream teams (e.g. Data Science, Fleet... 
    Senior
    Full time
    Temporary work
    Work at office
    Immediate start
    Relocation package

    Zoox

    San Mateo, CA
    6 days ago
  • $273k - $290k

     ...are at a pivotal inflection point.We are looking for a Senior Director of Quality Assurance to build a pragmatic, inspection-ready quality function...  ...week or one full week per month.ResponsibilitiesQuality Management SystemOwn the Operating System: Lead the evolution of... 
    Senior
    Home office
    Flexible hours
    3 days per week

    Insitro

    South San Francisco, CA
    3 days ago
  •  ...cancer and autoimmune disease. Led by a management team with significant experience in...  ...milestones, we are seeking a Senior Director of Quality Systems and Compliance to shape and lead...  ...Manufacturing, Regulatory, and Clinical Quality Assurance to foster a culture of quality and... 
    Senior
    Work at office
    Local area
    Remote work
    2 days per week

    Allogene Therapeutics

    South San Francisco, CA
    1 day ago
  •  ...employment. Position Director/Senior Director of Quality Operations Location South San Francisco...  ...candidate to join our Quality Assurance (QA) team. Our ideal candidate is a self...  ...through effective quality risk management, supports efficient and reliable manufacturing... 
    Senior

    Neurona Therapeutics

    South San Francisco, CA
    1 day ago
  • $280.2k - $319.8k

     ...Senior Director Quality Control Nurix Therapeutics is a clinical stage biopharmaceutical company focused on the discovery development and...  ...molecule QC strong regulatory acumen and proven experience managing external CDMO and CTL relationships. This role will represent... 
    Senior
    Full time
    For contractors

    Nurix

    Brisbane, CA
    11 days ago
  • Cytovale, Inc. in South San Francisco, CA is seeking a Head of Quality and Regulatory to own the QMS and serve as the Management Representative. This senior leadership role partners with Regulatory and Operations to drive compliant design, manufacturing, and post-market... 
    Senior

    Cytovale

    South San Francisco, CA
    2 days ago
  • Neurona Therapeutics, a clinical stage biotechnology company in South San Francisco, seeks a Director/Senior Director of Quality Assurance - Medical Device. The role leads QA activities for the device portion of a combination product, shaping quality systems and compliance... 
    Senior

    Neurona Therapeutics

    South San Francisco, CA
    2 days ago
  • Sr. Project Manager - Quality Management Systems Full-time We are focused on imparting effective business staffing services through high level...  ...lead Description: We're seeking a talented, multi-faceted Senior IT Project Manager who is enthusiastic about working in the... 
    Senior
    Full time

    360 IT Professionals

    South San Francisco, CA
    2 days ago
  •  ...Responsibilities Manage core QMS programs including deviations, investigations, CAPAs...  ...with internal stakeholders Develop quality metrics, perform trending analysis, and...  ...~6+ years quality systems or quality assurance background ~ Demonstrated eQMS implementation... 
    Senior

    Nurix Therapeutics

    Brisbane, CA
    a month ago
  • Genentech, a member of the Roche group, is seeking a Senior Quality Lead in Pharma Development Quality (PDQ) to develop QA strategies and lead...  ...preferred, and the ability to influence stakeholders and manage regulatory inspections across global teams. #J-18808-Ljbffr F... 
    Senior
    Remote work

    F. Hoffmann-La Roche AG

    South San Francisco, CA
    5 days ago
  •  ...Corcept Therapeutics seeks a Senior Manager of Clinical Quality Assurance to lead quality operations and compliance activities supporting clinical studies. The role involves audit planning, GCP audits, risk management, and regulatory oversight in a hybrid position based... 
    Senior

    Corcept Therapeutics

    Redwood City, CA
    25 days ago
  •  ...Vaxcyte seeks an experienced Senior Manager of Clinical Quality Assurance to lead quality investigations, audits, and compliance activities across clinical development programs. The role requires expertise in regulatory standards, quality management systems, and clinical... 
    Senior

    Vaxcyte

    San Carlos, CA
    a month ago

Do you want to receive more vacancies?

Subscribe and receive similar vacancies to Senior Manager, Quality Assurance. Be the first to apply!