出海雷达

Quality Compliance Senior Manager

职能支持限定地区(需当地身份)与中国几乎无重叠,需长期倒时差
公司Amgen
薪资$132,037 - $178,638/年
工作地点United States
地域资格限定地区(需当地身份)
时区要求与中国几乎无重叠,需长期倒时差
用工类型generous_pto
发布时间2 天前
数据来源4dayweek.io
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注意地域限制:该职位明确限定在 United States 招聘。如果你是位于中国大陆的求职者,通常需要当地工作身份才能投递,或需与雇主确认是否接受独立合同(Contractor)形式合作。
作息提示:与中国几乎无重叠,需长期倒时差。
关于本页中文:职位描述由本机离线模型翻译,属机器翻译,供快速判断用;正式沟通与投递请以英文原文为准。官方翻译通道恢复后会自动重译升级。

### **职业类别**质量## **工作描述**加入阿姆根服务患者的使命 在阿姆根,如果你觉得自己是更大的东西的一部分,那是因为你。我们共同的任务为患有严重疾病的病人提供服务,驱动了我们的一切。自1980年以来,我们帮助生物技术世界开拓在打击世界上最艰难的疾病中。阿姆根正在推进广泛和深入的药品管道和医疗组合来治疗心脏病,肥胖和肥胖相关条件,罕见疾病,炎症状况和癌症。作为阿姆根团队成员,你将有助于对患者的生活产生持久影响,因为我们研究,制造和提供创新药物来帮助人们过得更长,更满意的生活。我们的获奖文化是合作,创新的,基于科学。如果你热衷于挑战和它们所带来的机会,你将成为阿姆根组的一部分。加入我们并改变病人生活,同时改变你的职业生涯。**质量合规高级经理** **你会做什么**让我们这样做!让我们改变世界!高级经理领导 QIC 集成质量监督运营模式和管理的信号到行动生命周期,通过该系统来审查,文本化,分类,路由,监控和关闭 QIC 创建的信号,趋势,仪表板输出以及新兴质量见解。这个角色领导了 QuIC 团队并建立了商业标准,审查程序,治理投入,决策途径和跨功能工作方式,这些方法需要将 QIC 纳入研发质量监管中。**重点责任** - 负责 QuIC 日常运作,管理职责层面质量监测的专业团队。- 拥有并不断完善 QuIC 运营模式,包括审查序列,信号分类,文档预期,升级途径,行动跟踪和治理程序。- 为评估仪表板输出,质量指标,趋势,异常,门漏洞和其他 QuIC 生成的信号建立一致的审查节奏和业务标准。- 领导对仪表板产出的回顾和优先考虑,质量计量,趋势和异常以及门漏洩以确定需要进一步评估或后续的问题。- 将复杂的质量信息翻译,包括偏差,CAPA,审核和检查见解,操作。

查看英文原文

### **Career Category**

Quality

### **Job Description**

Join Amgen’s Mission of Serving Patients

At Amgen, if you feel like you’re part of something bigger, it’s because you are. Our shared mission—to serve patients living with serious illnesses—drives all that we do.

Since 1980, we’ve helped pioneer the world of biotech in our fight against the world’s toughest diseases. Amgen is advancing a broad and deep pipeline and portfolio of medicines to treat heart disease, obesity and obesity-related conditions, rare diseases, inflammatory conditions and cancer.  As a member of the Amgen team, you’ll help make a lasting impact on the lives of patients as we research, manufacture, and deliver innovative medicines to help people live longer, fuller happier lives.

Our award-winning culture is collaborative, innovative, and science based. If you have a passion for challenges and the opportunities that lay within them, you’ll thrive as part of the Amgen team. Join us and transform the lives of patients while transforming your career.

**Quality Compliance Senior Manager**

**What you will do**

Let’s do this! Let’s change the world! The Senior Manager leads the Quality Intelligence Center (QuIC) integrated quality oversight operating model and the governed signal-to-action lifecycle through which QuIC-generated signals, trends, dashboard outputs, and emerging quality insights are reviewed, contextualized, triaged, routed, monitored, and closed.

The role leads the QuIC team and establishes business standards, review routines, governance inputs, decision pathways, and cross-functional ways of working required to embed QuIC into R&D Quality oversight.

**Key responsibilities**

- Lead the day-to-day operation of the QuIC function and manage a professional team responsible for portfolio-level quality monitoring.
- Own and continuously improve the QuIC operating model, including review cadence, signal triage, documentation expectations, escalation pathways, action tracking, and governance routines.
- Establish consistent review cadences and business standards for evaluating dashboard outputs, quality metrics, trends, anomalies, threshold breaches, and other QuIC-generated signals.
- Lead the review and prioritization of dashboard outputs, quality metrics, trends, anomalies, and threshold breaches to identify issues requiring further assessment or follow-up.
- Translate complex quality information, including deviations, CAPAs, audit and inspection insights, operational metrics, and related evidence, into clear, governance-ready summaries, recommendations, and escalations.
- Ensure that significant findings are appropriately documented, escalated, and routed to accountable process owners and cross-functional stakeholders.
- Define and propose QuIC business rules, operating standards, documentation expectations, escalation pathways, and workflow requirements; ensure changes requiring controlled approval are reviewed through the appropriate accountable Quality governance.
- Partner with R&D Quality, Global Development Operations, and other stakeholders to ensure QuIC insights are understood and acted upon.
- Lead process improvements and provide business leadership for QuIC enhancements, including signal definitions, thresholds, business rules, data-quality expectations, training, and adoption activities.
- Monitor the effectiveness, timeliness, quality, and capacity of oversight activities and implement practical improvements where needed.
- Ensure activities comply with applicable GxP, quality-system, data-governance, and internal procedural requirements.

**What we expect of you**

We are all different, yet we all use our unique contributions to serve patients. The dynamic professional we seek is an individual with these qualifications.

**Basic Qualifications:**

- Doctorate degree and 2 years of Quality experience OR
- Master’s degree and 4 years of Quality experience OR
- Bachelor’s degree and 6 years of Quality experience OR
- Associate’s degree and 10 years of Quality experience OR
- High school diploma / GED and 12 years of Quality experience

**Preferred Qualifications:**

- Bachelor’s degree in scientific, clinical, quality, data, or related discipline, with substantial relevant experience in R&D Quality, clinical development, clinical operations, quality systems, risk management, or centralized monitoring.
- Demonstrated experience leading and developing professional employees or leading complex cross-functional teams.
- Strong experience interpreting quality, operational, or risk data and converting findings into clear recommendations, escalations, and follow-up actions.
- Working knowledge of GCP, quality-risk management, issue management, CAPA and deviation processes, audit and inspection readiness, and quality governance.
- Strong communication, stakeholder-management, organizational, and decision-making skills.
- Experience as an R&D Quality process owner or in quality oversight across deviations, CAPAs, audits, inspections, management review, or risk-management processes.
- Experience with QMS platforms, dashboards, data visualization, data quality, business analysis, user acceptance testing, or digital-product implementation.
- Experience with risk-based quality management, centralized monitoring, KRIs, QTLs, CSM, or signal-based quality oversight.
- Experience working with AI-enabled analytics or digital quality products, including the ability to critically evaluate system-generated insights and apply appropriate human judgment.
- Experience leading operational change in a global matrix environment.

**What you can expect of us**

As we work to develop treatments that take care of others, we also work to care for your professional and personal growth and well-being. From our competitive benefits to our collaborative culture, we’ll support your journey every step of the way.

The expected annual salary range for this role in the U.S. (excluding Puerto Rico) is posted. Actual salary will vary based on several factors including but not limited to, relevant skills, experience, and qualifications.

In addition to the base salary, Amgen offers a Total Rewards Plan, based on eligibility, comprising of health and welfare plans for staff and eligible dependents, financial plans with opportunities to save towards retirement or other goals, work/life balance, and career development opportunities that may include:

- A comprehensive employee benefits package, including a Retirement and Savings Plan with generous company contributions, group medical, dental and vision coverage, life and disability insurance, and flexible spending accounts
- A discretionary annual bonus program, or for field sales representatives, a sales-based incentive plan
- Stock-based long-term incentives
- Award-winning time-off plans
- Flexible work models where possible. Refer to the Work Location Type in the job posting to see if this applies.

Apply now and make a lasting impact with the Amgen team.

**careers.amgen.com**

In any materials you submit, you may redact or remove age-identifying information such as age, date of birth, or dates of school attendance or graduation. You will not be penalized for redacting or removing this information.

**Application deadline**

Amgen does not have an application deadline for this position; we will continue accepting applications until we receive a sufficient number or select a candidate for the position.

Sponsorship

Sponsorship for this role is not guaranteed.

As an organization dedicated to improving the quality of life for people around the world, Amgen fosters an inclusive environment of ethical, committed and highly accomplished people who respect each other and live the Amgen values to continue advancing science to serve patients. Together, we compete in the fight against serious disease.

Amgen is an Equal Opportunity employer. We make all employment decisions without regard to race, color, religion, sex or any other characteristic protected by applicable law.

We provide reasonable accommodations to applicants and employees with disabilities, consistent with legal requirements. Please contact us to request accommodation.

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**Salary Range**

132,037.30USD -178,638.70 USD

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