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

Associate Director, Quality Assurance, New Acquisitions

$182.07k - $235.62k

Jobleads-US

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 Description

AtGileadour 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 an Associate Director Quality Assurance at Gilead, you will be a member of the API/OSD/Packaging group. This role is responsible for supporting initial integration of new asset acquisitions into Gilead systems. The role acts as a leader providing hands-on support as well as giving guidance to other QA staff to ensure new product assets are available quickly and compliantly.

Key Responsibilities:

  • Acts as the overall responsible QA person for transition of small and large molecule Due Diligence assets to active Gilead programs.
  • May be the QA lead on Due Diligence projects and ensures high performance and consistency among other Due Diligence QA leads.
  • This role may have direct reports but will also provide leadership for staff from other QA teams supporting newly acquired assets.
  • Works closely with Product Strategy Team leads to ensure adequate QA coverage on new assets and to ensure onboarding and integration strategy is defendable.
  • Supports QA staff on Due Diligence teams and new asset Product Strategy teams to assess and highlight risks and ensure proper communication of risks and proposed mitigations.
  • Responsible for providing guidance on interpretation and application of existing and new US requirements pertaining to clinical and commercial phase programs.
  • Manage or provide support for QMS records such as deviations (internal & external), CAPAs & Change Controls related to onboarding and integration activities.
  • Participate in developing/approving Standard Operating Procedures (SOPs) and other types of documentation to ensure quality objectives are met.
  • Participate in the development & delivery of training programs relevant to Due Diligence and onboarding.
  • Conduct/participate in gap analyses and risk assessments of processes & procedures against relevant guidelines as well as corporate standards.
  • Participate in, or where relevant lead, local and corporate projects, and process improvement initiatives, as required.

Knowledge, Experience & Behaviors:

  • 10+ years of relevant experience in the pharmaceutical industry and a BS or BA OR
  • 8+ years of relevant experience in the pharmaceutical industry and a MS OR
  • 5+ years of relevant experience in the pharmaceutical industry and a PhD
  • Deep knowledge and experience in quality assurance in a highly regulated manufacturing environment.
  • Experience in asset acquisition due diligence, product and site assessments, and risk management.
  • Demonstrates a highly developed knowledge of clinical phase quality and compliance requirements, and an understanding of current industry trends.
  • Capable of assessing and communicating the impact of risks to the business.
  • Ability to engage and manage multiple stakeholders to achieve objectives.
  • Demonstrates excellent influencing and negotiation skills.
  • Excellent verbal, written and interpersonal skills are required.
  • Practiced in systematic approaches to prioritization, problem solving, and critical thinking.

People Leader Accountabilities:

  • Create 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: $182,070.00 - $235,620.00. 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 ACT YOUR RIGHTS UNDER THE FAMILY AND MEDICAL LEAVE ACT

Gilead 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.

#J-18808-Ljbffr Jobleads-US
Vacancy posted 2 days ago
Similar jobs that could be interesting for youBased on the Associate Director, Quality Assurance, New Acquisitions in Foster, CA vacancy
  • $190k - $205k

     ...improvement of policies and procedures to maintain quality standards aligned with global regulatory...  ...end-to-end implementation and rollout of new modules within Veeva, ensuring alignment...  ...cross-functional stakeholders (Quality Assurance, Manufacturing, Supply Chain, and IT) to... 
    Suggested
    Local area

    Mirum Pharmaceuticals

    Foster, CA
    1 day ago
  • $182.07k - $235.62k

     ...improving the lives of patients for generations to come. The Associate Director, Quality Assurance - GMP Operations provides senior Quality leadership and...  ...compliance through design, startup, and operation of a new, state-of-the-art Single Use DS Biologics Manufacturing facility... 
    Suggested
    Full time
    Contract work
    For contractors
    Local area

    GILEAD Sciences

    Foster, CA
    3 days ago
  • $186k - $233k

     ...inhibitor, are currently in clinical development. As a new member of the Revolution Medicines team, you will join other...  ...in the RAS signaling pathway.The Opportunity:The Associate Director, GMP Quality Assurance will provide quality oversight and decision-making authority... 
    Suggested
    Full time
    Contract work
    Work at office
    Local area

    Revolution Medicines

    Redwood City, CA
    3 days ago
  •  ...possible, together.Job DescriptionAssociate Director, Global Supplier QualityPosition SummaryThe Associate Director, Global Supplier Quality serves as the global program owner...  ...with 10+ years of experience in Quality Assurance, Supplier Quality, Quality Systems, Compliance... 
    Suggested
    Full time
    Contract work
    For contractors
    Local area

    GILEAD Sciences

    Foster, CA
    2 days ago
  • $186k - $233k

     ...inhibitor, are currently in clinical development. As a new member of the Revolution Medicines team, you will join...  ....The Opportunity:Revolution Medicines is seeking an Associate Director, Clinical Quality Assurance, who will play a key role within Quality Assurance and... 
    Suggested
    Full time
    Local area

    Revolution Medicines

    Redwood City, CA
    3 days ago
  • $186k - $233k

     ...currently in clinical development. As a new member of the Revolution Medicines team,...  ...pathway.The Opportunity:Lead the Global Quality Systems Monitoring & Excellence program to...  ...preferred.10+ years of progressive Quality Assurance/Quality Systems experience in the biotechnology... 
    Full time
    Local area

    Revolution Medicines

    Redwood City, CA
    1 day ago
  • $192.7k - $226.7k

     ...Redwood City, California. To learn more, visit The Associate Director of Clinical Quality Assurance (CQA) is a lead member of the CQA team and will lead and...  ...oversight throughout the study lifecycle Evaluate new processes and initiatives impacting clinical programs/... 
    Full time
    Work at office
    3 days per week

    Socket.dev

    Redwood City, CA
    2 days ago
  • $156k - $220k

     ...expanding the innovation frontier for new therapeutic development. Backed by...  ...is seeking an experienced and driven Associate Director of Global Quality to provide hands-on quality...  ...Reporting to the SVP of Quality Assurance & Regulatory Affairs, the Associate... 
    Full time
    Contract work
    Temporary work
    Part time
    Local area
    Remote work

    Antheia, Inc.

    Menlo Park, CA
    2 days ago
  • $186k - $233k

     ...inhibitor, are currently in clinical development. As a new member of the Revolution Medicines team, you will join other...  ...the RAS signaling pathway. The Opportunity: The Associate Director, GMP Quality Assurance will provide quality oversight and decision-making... 
    Full time
    Contract work
    Work at office
    Local area

    Jobleads-US

    Redwood City, CA
    6 hours ago
  • $171k - $211k

     ...Location: South San Francisco, CA. Position Summary IDEAYA is seeking a talented and highly motivated Associate Director, Quality Management Systems (QMS) with a passion for new cancer therapy development. This role will be responsible for leading the QMS function and for... 
    Contract work
    Temporary work
    For contractors
    Work at office
    Local area
    Work from home

    Initial Therapeutics, Inc.

    South San Francisco, CA
    1 day ago
  • $186k - $233k

    Associate Director, Global Patient Safety Quality and Compliance - Pharmacovigilance Revolution Medicines is a clinical...  ...treatment strategies. As a new member of the Revolution Medicines...  ...Science, Regulatory Affairs, Quality Assurance, Medical Affairs, and other departments... 
    Contract work

    Revolution Medicines

    Redwood City, CA
    3 days ago
  •  ...broad spectrum of retinal diseases. We are focused on bringing new science to the design and manufacture of next‑generation retinal...  ...role is responsible for developing, implementing, and managing Quality operations system in the organization to ensure compliance of biological... 

    Kodiak Sciences

    Palo Alto, CA
    3 days ago
  • $265k - $331k

     ...clinical development. As a new member of the Revolution Medicines...  ...Opportunity:The Executive Director, GxP Quality & Compliance is a senior...  ...with PDM, Quality Assurance, Regulatory Affairs, Clinical...  ...launches, technology transfers, acquisitions, business integrations,... 
    Full time
    Local area

    Revolution Medicines

    Redwood City, CA
    1 day ago
  •  ...the role: We are seeking a highly motivated Associate Director, Quality Engineer/Data Science to work in this exciting new area of allogeneic cell therapy. In this role...  ...submissions and inspections, including assuring inspection readiness. Support root cause investigations... 
    Full time
    Local area

    Allogene Therapeutics

    South San Francisco, CA
    a month ago
  •  ...Revolution Medicines seeks a senior quality leader to provide GMP QA oversight for DS/DPI development, manufacturing and testing. You will partner with Technical Operations, CMC, Regulatory, and external CDMOs to ensure product quality, data integrity, and timely release... 

    Jobleads-US

    Redwood City, CA
    6 hours ago
  • $80 - $93 per hour

    Job Title : Associate Director, Quality Location : Hybrid Reports to : Vice President, Head of Regulatory and Quality Full/Part-Time : Full-Time...  ...Associate Director of Quality is responsible for managing quality assurance activities, providing strategic oversight of the... 
    Hourly pay
    Full time
    Temporary work
    Part time

    Socket.dev

    South San Francisco, CA
    2 days ago
  • Kodiak Sciences in Palo Alto, CA is seeking a Quality Assurance professional to develop and manage the quality operations system, ensuring cGMP compliance and regulatory readiness across the organization. This on-site role requires coordinating with cross-functional teams... 

    Kodiak Sciences

    Palo Alto, CA
    3 days ago
  • $210.38k - $272.25k

     ....Job DescriptionJob Summary: The Product Quality Lead (PQL) supports one or more assigned...  ...and drug product technology transfer and new product launches. Ensure inspection readiness...  ..., manufacturing processes, and associated quality considerations. Experience working... 
    Full time
    For contractors
    Local area

    GILEAD Sciences

    Foster, CA
    3 days ago
  • $190k - $205k

     ...get it done, and have fun, seriously.POSITION SUMMARYThe Associate Director of GCP/GVP/GLP-QA is responsible for supporting Mirum’s clinical...  ...study management team; managing activities involving GCP quality assurance and compliance with applicable regulatory requirements;... 
    Contract work
    Local area

    Mirum Pharmaceuticals

    Foster, CA
    3 days ago
  • $229k - $268k

     ...for an energetic and talented individual to join our Quality Assurance team as a Senior Director. This role carries dual accountability: providing direct...  ...will be the QA oversight of QC activities associated with Vaxcyte’s PCV Polysaccharides and Drug Substances... 
    Contract work

    Vaxcyte

    San Carlos, CA
    1 day ago
  • $211k - $264k

     ...inhibitor, are currently in clinical development. As a new member of the Revolution Medicines team, you will...  ...mutations in the RAS signaling pathway.The Opportunity:The Director, Good Laboratory Practice Quality Assurance (GLP QA) is responsible for ensuring Good Laboratory... 
    Full time
    Local area

    Revolution Medicines

    Redwood City, CA
    4 days ago
  • $240k - $300k

     ...geographic location.Position Summary:We are seeking a Senior Director of GMP Quality Assurance (QA) to serve as a senior quality leader responsible for...  ...be eligible for an annual performance incentive bonus, new hire equity, and ongoing performance-based equity. Structure... 
    Contract work

    Structure Therapeutics

    South San Francisco, CA
    3 days ago
  •  ...Senior Director, Quality As the Senior Director, Quality, you will serve as the quality authority for Sagimet Biosciences, leading and...  ...audits, host regulatory agency inspections, and manage all associated audit responses and CAPAs. ·Oversee deviation management,... 

    Sagimet Biosciences

    San Mateo, CA
    2 days ago
  • $210.38k - $272.25k

     ...their aspirations. Join Gilead and help create possible, together.Job DescriptionDirector, Global Supplier Quality Management ProgramPosition ImpactThe Director, Global Supplier Quality Management Program serves as the Global Process Owner (GPO) for Supplier Quality Management... 
    Full time
    For contractors
    Local area

    GILEAD Sciences

    Foster, CA
    1 day ago
  • $194k - $199k

     ...mission focused on improving quality of life, increasing...  ...additional offices in California, New Jersey, the UK, and Ireland....  ...Miami, FL. Overview Of Role The Associate Director, Regulatory Affairs, CMC is...  ...contact Summit’s Talent Acquisition team at ****@*****.***... 
    Work at office

    Summit Therapeutics, Inc.

    Palo Alto, CA
    3 days ago
  • $101.7k - $152.5k

     ...and creativity.Senior Experience Planning & Merchandising Associate Manager San Mateo, CA (Hybrid)Role overview:Our team operates...  ...services. This wider group strives to maximise new subscriber acquisition and retention and provide a compelling reason for people to... 
    Seasonal work

    Sony Interactive Entertainment America

    San Mateo, CA
    2 days ago
  • $200k - $230k

     ...Description:Allogene is seeking a Product Quality Leader (PQL) to oversee Allogene’s CAR T...  ...coordination of Quality related activities associated with drug substance/drug product...  ...bridging strategies for the implementation of new analytical methods during the course of the... 
    Full time
    Contract work
    Work experience placement
    Work at office
    Local area

    Allogene Therapeutics

    South San Francisco, CA
    2 days ago
  • $157.59k - $203.94k

     ...lives of patients for generations to come.  As the Sr Manager Quality Assurance - GMP Operations at Gilead, you will provide Quality leadership...  ...GMP compliance through design, startup, and operation of a new, state-of-the-art Single Use DS Biologics Manufacturing facility... 
    Full time
    Contract work
    For contractors
    Local area

    GILEAD Sciences

    Foster, CA
    3 days ago
  • $300k - $350k

     ...demonstrating integrity, accountability, equality and clarity across communications and decision making.Summary:The Executive Director, Quality Assurance, External Manufacturing is responsible for leading the External Manufacturing Quality function and executing the quality... 
    Contract work
    Relocation
    Relocation package
    2 days per week
    3 days per week

    Vaxcyte

    San Carlos, CA
    2 days ago
  • $174k - $203k

     ...communications and decision making.Summary:The Associate Director, Process Validation and Risk Management...  ..., and processes in collaboration with Quality.Lead cross-functional risk assessments...  ...and creative approach to developing new, innovative ideas that will stretch the... 

    Vaxcyte

    San Carlos, CA
    2 days ago

Do you want to receive more vacancies?

Subscribe and receive similar vacancies to Associate Director, Quality Assurance, New Acquisitions. Be the first to apply!