Senior Director Quality Intelligence and Systems

Reposted 18 Days Ago
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South San Francisco, CA
In-Office
236K-295K
Senior level
Biotech
The Role
The Sr. Director of Quality Intelligence and Systems is responsible for optimizing quality systems, ensuring compliance, and embedding a culture of proactive quality management across the organization.
Summary Generated by Built In

Alumis Inc. is a precision medicines company with the mission to transform the lives of patients with autoimmune diseases. Even with treatment innovations of the last two decades, many patients with immunologic conditions continue to suffer - our goal is to fundamentally change the outcomes for these patients. 

Sr. Director, Quality Intelligence and Systems

Alumis is hiring a forward-thinking Senior Director of Quality Intelligence and Systems reporting to the Senior Vice President of Quality and Regulatory.  The Sr. Director is responsible to optimize quality systems and its management to fulfill the purpose of detection, maintenance, and correction of the underlying quality process of interest (e.g., documentation, training/qualification, deviation, CAPA, change control, supplier management, product complaints). In addition, this role interprets, integrates, and applies compliance signals to ensure compliance adherence that is informed by the latest quality regulations, guidance, or expectations.

This position requires extensive expertise in the GxPs and relevant regulations. The successful candidate drives, promotes, and embeds a culture of ethics, integrity, and proactive quality management.  The candidate provides support to ensure that the quality function maintains the standards expected by the health authorities and facilitates “Right-First-Time” and phase appropriate decisions through risk and knowledge management processes. 

ESSENTIAL DUTIES & RESPONSIBILITIES

  • Partner closely with the SVP, Quality and Regulatory to drive execution of strategic priorities and departmental planning.
  • Oversee and manage the Quality Systems group, including but not limited to document control, training, quality supplier management deviation, CAPA, and change control, maintaining content and execution ownership with the functional areas.
  • Oversee the global Quality Systems strategy, integrating data, insights, and compliance signals to enable proactive, risk-based decision-making.
  • Lead and align cross-functional initiatives that advance quality system maturity, inspection readiness, and operational excellence.
  • Act as a strategic liaison between the Quality Systems function and the business.
  • Lead Quality Governance processes (QSMR, SOGO, ITQuality..etc.)  that elevate enterprise visibility, foster a right-first-time mindset, and support a high-performing quality culture.
  • Lead development and tracking of Quality KPIs to measure performance and support continuous improvement.
  • Act as the “Chief of Staff” for the Quality team. Facilitate the operating rhythm of the Quality leadership team, ensuring alignment and follow-through on key decisions.
  • Develop and maintain a comprehensive knowledge of compliance signals that inform strategic quality decisions and initiatives.
  • Bridge quality insights into actionable strategies to ensure the company remains at the forefront of industry compliance and quality standards.
  • Drives continuous improvement initiatives based on quality trends and intelligence.
  • Develop and implement quality strategies and systems that integrate quality intelligence to enhance compliance and operational efficiency.
  • Collaborates with cross-functional teams to ensure alignment of quality objectives and acts as a liaison with suppliers to address quality systems issues.
  • Author/review or approve appropriate quality documents including SOPs, quality systems records, and health authority responses. 
  • Promote a culture of proactive quality management and health authority compliance ensuring quality mindset and quality excellence approach throughout the organization.
  • Uses data to recognize trends, shape strategy, and inform activities using dashboards and other communication vehicles.

EDUCATION & EXPERIENCE

  • Bachelor’s degree, advanced degree preferred, in a scientific discipline, communication, business, or training with a minimum of 12 years of industry experience, including relevant combination of education, experience, or training in GxP, quality assurance, quality intelligence, or Life Sciences.
  • Five (5) plus years of management experience leading teams and influencing stakeholders internal and external.
  • Experience in implementing and managing electronic quality management systems (eQMS), including document management, and learning management systems.
  • Experience interacting with health authorities through supporting inspection with on demand evidence fulfillment or interaction with the investigator, and/or writing responses to findings/observation.
  • Familiarity with the Quality Management Maturity Model.
  • Experience with an emerging virtual company.

KNOWLEDGE/ SKILLS/ ABILITIES

  • Demonstrates strong knowledge of global GxP expectations, regulations, and quality trends across the product development lifecycle – bench to bedside.
  • Demonstrates the ability to organize, sequence tasks per priority, delegate, thrive in a fast-paced, deadline driven environment, and communicate meaningful expectations.
  • Develops key quality metrics, including quality system, process, and people metrics, that provides insights and foresights in identifying and addressing quality systems or product concerns or opportunities.
  • Exhibits strong interpersonal skills, with experience in leading high-performance team and cross functional projects including a successful track record working with senior management and other key stakeholders.
  • Establishes effective escalation paths that communicates a current context and then a proactive, evidence-based solution while calibrating management and supplier awareness and action.
  • Demonstrates a goal orientation with a completion mindset that incorporates the ability to troubleshoot, resolve problems, and learn from and then share the learning with others.
  • Advocates continuous improvement to quality processes, well-trained workforce, streamlined business processes, and appropriately structured quality operations.
  • Demonstrates a self-organizing orientation that leverages minimal supervision, constructs priorities and deadlines based on the needs of the business and quality requirements and motivates and influences others. 
  • Recruits, develops, trains, mentors, coaches, and counsels team members for success and high performance.
  • Be willing to travel 5% of the time.

ALUMIS VALUES

  • We Elevate
  • We Challenge
  • We Nurture

This position is located in South San Francisco, CA. At this time, we are not considering remote applicants.

Alumis Inc. is an equal opportunity employer. If you are hired, we will require you to prove that you have received the primary series of an FDA-approved or authorized COVID -19 vaccine and at least one booster or have a valid religious or medical reason not to be vaccinated.

The salary range for this position is $236,000-$295,000 USD annually. This salary range is an estimate, and the actual salary may vary based on the Company’s compensation practices.  

Alumis compensation packages include generous stock option grants for all employees as well as an annual bonus program.  

Other benefits include:

  • Health insurance premiums paid at 90% for employee, 80% for dependents
  • Free access to Genentech Bus & Ferry Share program
  • $100 monthly cell phone stipend
  • Unlimited PTO for Exempt employees
  • Free onsite gym and a kitchen stocked with yummy snacks and drinks!

We are a hard-working, collaborative team on a mission to transform patient’s lives-- and we aspire to elevatechallenge and nurture one another along the way.

*Lab personnel are generally onsite 4-5 days/week.




Top Skills

Document Management Systems
Electronic Quality Management Systems
Gxp
Quality Assurance
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The Company
HQ: South San Francisco, California
162 Employees
Year Founded: 2021

What We Do

At Alumis, our goal is to significantly improve the lives of patients by replacing broad immunosuppression with targeted therapies.

We recognize that patients living with immune-mediated diseases need alternatives to currently available therapies. Despite recent advances and innovations in the treatment of immune-mediated diseases, many patients continue to suffer, cycling through currently approved therapies while looking for a solution that alleviates the debilitating impact of their disease without life-limiting side effects.

Addressing the needs of these patients is why we exist. We are pioneering a precision approach that leverages insights we derive from powerful data analytics to select the right target, right molecule, right indication, right patient, and right endpoint resulting in optimized outcomes for patients. We believe that combining our insights with an integrated approach to drug development will produce the next generation of treatments to address immune dysfunction.

Incubated by Foresite Labs, Alumis is led by a team of deeply experienced professionals who are devoted to transforming the lives of patients with immune-mediated diseases by developing a pipeline of transformative therapies.

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