招聘

Executive Director, Risk and Proactive Quality
United States - New Jersey - Parsippany
·
On-site
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Full-time
·
4d ago
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
The Executive Director, Risk and Proactive Quality is a senior enterprise Quality leader responsible for defining, governing, and advancing the global strategy for Quality Risk Management and Proactive Quality across the organization. This role serves as the Global Business Process Owner (BPO) for Risk and has direct leadership accountability for the Change Control, Medical Device & Combination Product Risk, and Proactive Human and Organizational Performance (HOP) global process owners.
This leader provides strategic direction and oversight to ensure that risk‑based thinking, proactive quality practices, and human‑centric performance principles are deeply embedded across the Pharmaceutical Quality System (PQS) and operations. The role is accountable for designing, implementing, and sustaining compliant, scalable, and efficient global processes that enable early risk identification, effective risk mitigation, and continuous improvement aligned with cGMP, ICH, and evolving global regulatory expectations.
As a member of the Central Quality leadership team, the Executive Director drives cultural transformation toward a systemic, proactive, and learning‑oriented quality organization, enabling robust decision‑making, operational excellence, and sustained regulatory compliance across a complex, multinational environment.
Key Accountabilities
Global Business Process Ownership and Governance
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Serve as Global Business Process Owner (BPO) for Quality Risk Management, with enterprise accountability for strategy, standards, performance, and continuous improvement.
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Provide executive leadership and oversight for the following global process owners:
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Change Control
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Medical Device and Combination Product Risk
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Proactive Human and Organizational Performance (HOP)
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Design, own, and approve global standards, policies, and procedures ensuring alignment with cGMP, ICH, and regulatory expectations across all markets.
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Ensure effective integration and alignment of risk, change, device/combination product, and human performance processes across the PQS and related business processes.
Risk and Proactive Quality Strategy
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Define and execute the global Proactive Quality and Risk Management strategy, enabling early risk identification, mitigation, and prevention across operations and the supply chain.
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Drive the evolution of organizational risk maturity, capability, and culture, embedding risk‑based thinking into decision‑making at all levels.
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Oversee the enterprise Quality Risk Register and development of the Operations Quality risk profile for senior leadership and management review forums.
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Ensure strong linkage between Quality Risk Management and broader enterprise and operational risk management frameworks.
Proactive Human and Organizational Performance (HOP)
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Provide strategic leadership to the Proactive HOP global process, ensuring effective integration of human‑centric risk mitigation approaches into quality and operational processes.
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Champion learning‑based, non‑punitive approaches that strengthen human performance, reduce error‑prone conditions, and enhance system reliability.
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Enable consistent application of HOP principles across sites, regions, and functions to support sustainable proactive quality outcomes.
Change Control and Device / Combination Product Risk Oversight
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Provide executive governance of the global Change Control process, ensuring changes are risk‑assessed, compliant, and effectively implemented across the PQS.
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Oversee Medical Device and Combination Product Risk Management, ensuring appropriate risk methodologies, lifecycle oversight, and regulatory alignment across development, manufacturing, and post‑market activities.
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Ensure strong cross‑functional collaboration with Technical, Regulatory, Safety, and Operations partners to manage complex product and process risks.
Leadership, Influence, and Stakeholder Engagement
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Lead and develop a global network of BPOs, subject matter experts, and process leaders through direct, matrix, and influence‑based leadership.
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Serve as a senior Quality representative in global governance forums, inspections, and regulatory interactions related to risk, change, and proactive quality.
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Actively monitor internal and external signals, including audit outcomes, inspection findings, deviations, complaints, and emerging regulatory trends, to inform strategy and priorities.
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Sponsor and lead transformational initiatives that leverage Lean principles, digital enablement, and innovative practices to improve process effectiveness and efficiency.
Typical People Management Responsibility
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Senior leader of multiple global process owners and expert teams
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Direct and indirect management of global, cross‑functional teams
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Matrix leadership across sites, regions, and functions
Global Remit
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Enterprise‑wide accountability with responsibility spanning all global markets and operating regions
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Regular engagement across multiple countries and cultures
Education, Qualifications, Skills, and Experience
Essential
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BS/BA degree with 16+ years or MS/MA/PhD with 14+ years experience in pharmaceutical quality, manufacturing, or a related scientific discipline
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Deep subject matter expertise in Quality Risk Management, with demonstrated success implementing global risk programs
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Extensive experience working across multiple areas of Quality within a regulated pharmaceutical environment
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Proven ability to lead through influence in complex, matrixed, multinational organizations
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Strong strategic thinking, communication, and stakeholder engagement capabilities
Desirable
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Experience leading large‑scale Quality or Operations transformation initiatives
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Experience with Human and Organizational Performance (HOP) and Proactive Human Dependent Process Improvement
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Expertise in Business Process Management, Lean, Six Sigma, or comparable continuous improvement methodologies
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Experience overseeing GxP IT systems and digital enablement of Quality processes
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Strong business acumen with the ability to analyze trends, assess risk, and build compelling business cases
The salary range for this position is:
Other US Locations: $255,425.00 - $330,550.00.
Bay Area: $281,010.00 - $363,660.00.
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:
https://www.gilead.com/careers/compensation-benefits-and-wellbeing
- 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 [Applicant Accommodations@gilead.com](mailto:Applicant Accommodations@gilead.com) for 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.
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关于Gilead Sciences

Gilead Sciences
PublicGilead Sciences, Inc. is an American biopharmaceutical company headquartered in Foster City, California, that focuses on researching and developing antiviral drugs used in the treatment of HIV/AIDS, hepatitis B, hepatitis C, influenza, and COVID-19, including ledipasvir/sofosbuvir and sofosbuvir.
10,001+
员工数
Foster City
总部位置
$85B
企业估值
评价
3.7
10条评价
工作生活平衡
2.5
薪酬
4.2
企业文化
3.0
职业发展
3.5
管理层
2.3
65%
推荐给朋友
优点
Good people and friendly work environment
Competitive compensation and benefits
Career growth opportunities
缺点
Poor management and leadership issues
Toxic culture and workplace stress
Limited work-life balance
薪资范围
34个数据点
Junior/L3
Mid/L4
Senior
Director
Junior/L3 · Program Manager
0份报告
$212,000
年薪总额
基本工资
-
股票
-
奖金
-
$180,200
$244,000
面试经验
42次面试
难度
3.2
/ 5
时长
14-28周
录用率
41%
体验
正面 64%
中性 21%
负面 15%
面试流程
1
Phone Screen
2
Technical Interview
3
Hiring Manager
4
Team Fit
常见问题
Technical skills
Past experience
Team collaboration
Problem solving
新闻动态
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Gilead Sciences, Inc. $GILD Position Raised by Asset Management One Co. Ltd. - MarketBeat
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Jim Cramer on Gilead Sciences: “I’d Hold On to It” - Yahoo Finance
Yahoo Finance
News
·
5d ago
Buy Signal Gilead Sciences Inc - 17 Apr 2026 @ 09:44 -> USD137.33
Ticker: **GILD** Exchange: **NASDAQ** Time: **17 Apr 2026 @ 09:44** Price: **USD137.33** Link: https://getagraph.com/NASDAQ/stock/live-signals/GILD/ENG
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5d ago
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