채용

Sr Director, Proactive Quality Human & Organizational Performance (HOP)
United States - California - Foster City
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On-site
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Full-time
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3d 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 Senior Director, Proactive Human & Organizational Performance (HOP) is a senior global Quality leader responsible for defining, governing, and deploying proactive quality approaches that strengthen human‑dependent processes and system reliability across the Pharmaceutical Quality System (PQS) and operations. This role serves as the Global Business Process Owner (BPO) for Proactive HOP, accountable for global standards, performance management, capability building, and continuous improvement of the Proactive HOP program.
The role reports directly to the Executive Director of Risk and Proactive Quality and partners closely with other Quality GPOs, Local and Functional Process Owners, and site leadership teams to embed Human Dependent Process Improvement (HDPI) and systems‑model thinking into process design, control strategies, and daily execution. The Senior Director champions learning‑based, non‑punitive practices that reduce error‑prone conditions, improve decision‑making, and enable sustained compliance and operational excellence aligned with cGMP and evolving global regulatory expectations.
Key Accountabilities Global Business Process Ownership and Governance (Proactive HOP)
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Serve as Global Business Process Owner (BPO) for Proactive HOP with enterprise accountability for strategy, standards, performance, and continuous improvement.
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Design, own, and approve global standards, policies, procedures, and supporting training/job aids ensuring alignment with cGMP, ICH, and regulatory expectations across all markets.
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Define global KPIs, monitor adherence and effectiveness, and drive global standardization, simplification, and sustained adoption through a global process network.
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Provide subject matter expert (SME) coaching and consultation to sites/regions on human‑centric risk mitigation and human‑dependent process design.
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Actively monitor signals of process performance (e.g., audit/inspection observations, issue management, deviations, complaints, and trend data) and escalate/correct systemic risks as required.
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Own inspection readiness and defense for the Proactive HOP program, including observation responses and sustained remediation where applicable.
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Manage interdependencies with other PQS processes/GPOs (e.g., risk management, deviations, change control, training, self‑inspection) to ensure end‑to‑end integration.
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Partner with IT system owners to maintain business requirements for enabling systems; ensure supporting Quality IT solutions meet GxP requirements and approve relevant changes/releases.
Integration and Delivery of Proactive Operations Quality Objectives
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Partner with global process owners/GPOs, and Local/Functional Process Owners to identify and implement proactive improvements that drive next‑level performance in human‑dependent processes (e.g., risk management, deviations, change control, self‑inspection, training).
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Co‑develop global and functional/site proactive operations objectives; support sites in defining locally relevant deliverables aligned to global priorities.
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Establish governance to track deliverables, benefits realization, and sustainability of improvements across the network.
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Lead and/or sponsor significant continuous improvement initiatives (e.g., HDPI acceleration, proactive risk assessment approaches, error‑proofing, and digital enablement) that improve effectiveness and efficiency.
Human & Organizational Performance (HOP) and Systems‑Model / HDPI Acceleration
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Build capability within regions to apply HOP/HDPI and systems‑model thinking proactively to quality systems, process execution, and controls to prevent impactful errors before they occur.
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Mentor and coach functional and site teams to modernize control strategies (e.g., focusing on true critical steps and error‑likely conditions vs. treating all steps as equal).
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Embed Proactive HOP principles into equipment and process design through partnership with engineering, technical, and operational stakeholders.
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Provide a balanced mix of remote and in‑person support (e.g., workshops, Gemba, coaching) to accelerate adoption and competency at manufacturing sites.
Proactive Tools, Training, and Community of Practice
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Develop and maintain global training curricula, certification requirements, and practical job aids for HOP/HDPI methods and proactive tools.
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Deliver and oversee train‑the‑trainer models to scale capability through functional/site champions.
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Facilitate sharing, calibration, and adoption of good practices and lessons learned across the network.
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Continuously seek user feedback and identify opportunities for simplification, automation, and error‑proofing to improve user experience and reduce manual burden.
Leadership, Influence, and External Engagement
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Lead through influence in a complex, matrixed environment, aligning stakeholders across sites and functions to deliver sustained proactive quality outcomes.
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Monitor external trends (e.g., regulatory expectations, industry guidance, emerging practices) and translate insights into updates to strategy, standards, and capability building.
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Represent the organization in external industry forums related to HOP and proactive quality, building benchmarks and partnerships that advance internal maturity.
Typical People Management Responsibility
- Senior leader of a global Proactive HOP process network with matrix accountability across sites and functions.
- Direct people management responsibility may include a small expert team and/or program resources (TBD), with broader influence‑based leadership across the network.
Global Remit
- Enterprise‑wide accountability spanning all global markets and operating regions.
- Regular engagement across multiple countries and cultures; expected travel approximately 25–35% (site support, workshops, governance, and external forums).
Education, Qualifications, Skills, and Experience Essential
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Bachelor’s degree and/or substantial relevant experience with 14+ years in pharmaceutical quality, manufacturing, engineering, or a related scientific discipline.
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Experience working cross‑functionally and cross‑culturally across the supply chain in a regulated environment.
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Demonstrated ability to influence and define global ways of working in complex, matrixed organizations.
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Strong risk‑based decision‑making skills and a systems mindset; able to translate insights into practical controls and behaviors.
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Excellent communication skills and ability to build relationships across a global network and with cross‑functional customers.
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Independence and ability to work with minimal supervision; strong planning, prioritization, and follow‑through.
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Subject matter expertise in Human & Organizational Performance (HOP) and Human Dependent Process Improvement (HDPI) and their proactive application.
Desirable
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Experience leading transformational change programs and capability‑building at scale.
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Understanding and experience in GMP change control and event/deviation management.
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Experience with Business Process Management and operating model design; change agent roles.
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Project/program management experience including governance, planning, and benefits realization.
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Experience with global GxP IT systems delivery and lifecycle management; digital enablement of quality processes.
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Strong business acumen and ability to assess trends/complex data and build robust business cases and impact analyses.
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Training and/or certification in Lean, Six Sigma, or comparable continuous improvement methodologies.
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Experience with DAI or similar structured decision‑making approaches.
The salary range for this position is: $243,100.00 - $314,600.00. 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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Gilead Sciences 소개

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+
직원 수
Foster City
본사 위치
$85B
기업 가치
리뷰
3.7
10개 리뷰
워라밸
2.5
보상
4.2
문화
3.0
커리어
3.5
경영진
2.3
65%
친구에게 추천
장점
Good people and friendly work environment
Competitive compensation and benefits
Career growth opportunities
단점
Poor management and leadership issues
Toxic culture and workplace stress
Limited work-life balance
연봉 정보
34개 데이터
Junior/L3
Mid/L4
Senior
Director
Junior/L3 · Program Manager
0개 리포트
$212,000
총 연봉
기본급
-
주식
-
보너스
-
$180,200
$244,000
면접 경험
42개 면접
난이도
3.2
/ 5
소요 기간
14-28주
합격률
41%
경험
긍정 64%
보통 21%
부정 15%
면접 과정
1
Phone Screen
2
Technical Interview
3
Hiring Manager
4
Team Fit
자주 나오는 질문
Technical skills
Past experience
Team collaboration
Problem solving
뉴스 & 버즈
Gilead Sciences, Inc. $GILD Shares Bought by GF Fund Management CO. LTD. - MarketBeat
MarketBeat
News
·
4d ago
Gilead Sciences, Inc. $GILD Position Raised by Asset Management One Co. Ltd. - MarketBeat
MarketBeat
News
·
4d ago
Jim Cramer on Gilead Sciences: “I’d Hold On to It” - Yahoo Finance
Yahoo Finance
News
·
4d 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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4d ago
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1