Regulatory Jobs
Hero Gradient Background
Amgen office buildings around a landscaped plaza at its Thousand Oaks, California headquarters
Amgen logo

New · posted Oct 21

Amgen · Biotechnology

Quality Compliance Senior Manager

  • Remote, US
  • Remote
  • Full-time
  • Manager
Save
EmploymentFull-time
LocationRemote, USRemote
Deadline

Open until filled

The role

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.

What you need

5 ways to qualify

  1. PhD

    + 2 years of experience

    Doctorate degree and 2 years of Quality experience OR

  2. or

    Master’s

    + 4 years of experience

    Master’s degree and 4 years of Quality experience OR

  3. or

    Bachelor’s

    + 6 years of experience

    Bachelor’s degree and 6 years of Quality experience OR

  4. or

    Associate

    + 10 years of experience

    Associate’s degree and 10 years of Quality experience OR

  5. or

    High school

    + 12 years of experience

    High school diploma / GED and 12 years of Quality experience

Basic Qualifications

    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.

    Preferred Qualificationsnice to have

    • 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'll 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.

    1. Lead the day-to-day operation of the QuIC function and manage a professional team responsible for portfolio-level quality monitoring.
    2. Own and continuously improve the QuIC operating model, including review cadence, signal triage, documentation expectations, escalation pathways, action tracking, and governance routines.
    3. Establish consistent review cadences and business standards for evaluating dashboard outputs, quality metrics, trends, anomalies, threshold breaches, and other QuIC-generated signals.
    4. Lead the review and prioritization of dashboard outputs, quality metrics, trends, anomalies, and threshold breaches to identify issues requiring further assessment or follow-up.
    5. Translate complex quality information, including deviations, CAPAs, audit and inspection insights, operational metrics, and related evidence, into clear, governance-ready summaries, recommendations, and escalations.
    6. Ensure that significant findings are appropriately documented, escalated, and routed to accountable process owners and cross-functional stakeholders.
    7. 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.
    8. Partner with R&D Quality, Global Development Operations, and other stakeholders to ensure QuIC insights are understood and acted upon.
    9. Lead process improvements and provide business leadership for QuIC enhancements, including signal definitions, thresholds, business rules, data-quality expectations, training, and adoption activities.
    10. Monitor the effectiveness, timeliness, quality, and capacity of oversight activities and implement practical improvements where needed.
    11. Ensure activities comply with applicable GxP, quality-system, data-governance, and internal procedural requirements.

    Pay and benefits

    $132,000 – $179,000 a year

    Employer provided
    How this compares

    132,037.30USD -178,638.70 USD

    What you can expect of us

    • 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.

    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:

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

    Working conditions

    Career Category

    Quality

    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.

    Equal opportunity, accessibility and legal noticesAmgen's statements, word for word

    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.

    Job intelligence

    The context around this role

    Live data · October 23, 2026

    Salary intelligence

    How the pay compares

    This role's midpoint is 2% above the US median for Quality Assurance roles at this level.

    This roleEmployer provided

    $132,000 to $179,000 a year

    Manager roles in the US111 roles publishing pay

    Middle half $132,000 to $167,500, median $153,000
    Annual base pay
    Annual base payLowMedianHigh
    This role$132,000—$179,000
    All US$132,000$153,000$167,500

    This role: Amgen's own published range. Comparisons: the base pay employers published on open Quality Assurance roles at the same level on Regulatory Jobs, October 23, 2026. Nothing is estimated.

    Career trajectory

    Where this role sits in Quality Assurance

    The general path across 927 open Quality Assurance roles on Regulatory Jobs, with the titles they carry most. Not Amgen's own promotion track.

    1. Earlier

      Associate & Specialist

      Often: Quality Engineer · Quality Technician

      $81K median251 open
    2. One step back

      Senior & Principal

      Often: Quality Engineer · Senior Quality Engineer

      $119K median394 open
    3. This role

      Manager

      Often: Manager, Quality Assurance · Quality Manager

      $153K median144 open
    4. Next step

      Director

      Often: Director, Quality · Associate Director, Quality Assurance

      $209K median121 open
    5. Later

      VP & Executive

      Often: AVP · DX Head of Regions Quality Management and Regulatory Affairs

      $302K median17 open

    Skills DNA

    What this role leans on

    How many of the posting's 33 duty, requirement and summary lines touch each area. The posting's emphasis, not a proficiency score.

    GMP and compliance: 4 linesLab testing and methods: 1 lineDocumentation and SOPs: 3 linesInvestigations and CAPA: 3 linesQuality systems and risk: 7 linesData and digital systems: 1 lineCollaboration and leadership: 11 linesGMPLab testingDocumentationInvestigationsQuality systemsData systemsTeamwork
    • Collaboration and leadership11
    • Quality systems and risk7
    • GMP and compliance4
    • Documentation and SOPs3
    • Investigations and CAPA3
    • Lab testing and methods1
    • Data and digital systems1

    Regulatory intelligence

    The rules behind this role

    Frameworks and standards this posting's work falls under, matched from its own words, each linked to the official source.

    Company hiring pulse

    Amgen on Regulatory Jobs

    32
    Open roles
    30
    Distinct roles
    6
    Locations

    By discipline

    • Quality22 69%
    • Regulatory8 25%
    • Compliance & Safety2 6%

    By level

    • Manager13 41%
    • Senior & Principal10 31%
    • Associate & Specialist6 19%
    See all 32 Amgen roles

    More roles at Amgen

    All 32 Amgen roles

    Similar Quality Assurance roles elsewhere

    Quality Compliance Senior Manager at Amgen

    Open until filled. $132K–$179K a year, employer provided.

    Job alerts