Senior Global Process Owner - Risk-Based Quality Management

Posted Yesterday
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Hiring Remotely in Office, Machaze, Manica, MOZ
Remote
Senior level
Biotech • Pharmaceutical
The Role
Owns the end-to-end risk-based quality management process for global clinical development. Designs strategy, maintains compliant processes and controlled documentation, leads cross-functional improvement and change initiatives, and drives simplification, automation, and standardization. Oversees process risks, mitigations, performance monitoring, root-cause analysis, and FMEA activities while aligning clinical trial processes with regulatory and business requirements.
Summary Generated by Built In

Job Description Summary

Full time, Hybrid, #LI-HybridJoin a team that is redefining how Novartis delivers high‑quality medicines by integrating end‑to‑end trial process excellence with proactive, risk‑based quality management—powering smarter decisions, stronger data integrity, and faster impact for patients worldwide
As Senior Global Process Owner (Sr. GPO) you will have significant impact and accountability for designing and managing an end-to-end business process that is compliant with regulatory requirements and is fulfilling business needs across the end-to-end clinical trial process in Novartis drug Development.
The role drives adoption by working collaboratively with Global Line Functions, within a complex matrix, ensuring that processes meet both high design standards, regulatory compliance, and high levels of practicality. You will be an advocate for simplification and process automation.


 

Job Description

Major accountabilities:

1. End‑to‑End Process Ownership & Strategy

  • Accountable for the overall design, delivery, maintenance, and continuous improvement of the designated process(es).

  • Lead long‑term process strategy, ensuring alignment with regulatory expectations and business needs.

  • Anticipate internal/external changes and assess their impact on processes and supporting systems.

2. Cross‑Functional Collaboration & Process Improvement

  • Lead and support cross‑functional process improvement and change‑management initiatives.

  • Drive simplification, automation, and standardization across functions.

  • Ensure transformed processes can be executed globally by responsible line functions.

3. Governance, Documentation Oversight & Compliance

  • Ensure oversight and lifecycle management of controlled documents (SOPs, WPs, manuals) for the process.

  • Ensure coherence and harmonization across procedural documents within the process.

  • Oversee process‑related risks and ensure appropriate mitigation strategies.

  • Monitor performance trends, conduct root cause analysis/FMEAs when needed, and ensure appropriate risk management.

Minimum Requirements:
Education

Minimum: University degree in Life Science, quantitative science or business. Desirable qualifications in shared services, outsourcing, global sourcing. project management/Coaching, 6-Sigma, Lean education/training, Master of Business Administration or equivalent

Work Experience:

  • Extensive knowledge of end-to-end processes within clinical development, including supporting systems, regulations, and awareness of business changes.

  • Risk-based Quality Management process design and/or implementation essential

  • 10+ years Clinical Development or Clinical Operations experience, with a strong understanding of the clinical trial lifecycle.

  • Ability to anticipate and assess the impact of external and internal changes on the end-to-end process, supporting systems (and vice-versa), and associated training requirements.

  • Experience in effective process improvement.

  • Strategic thinker with the ability to contribute to long-term process improvements and operational planning.

  • Experience with process simplification and optimization, including improvements to quality documentation.

  • Demonstrated ability to collaborate effectively across functions, supporting performance improvements within the end-to-end clinical development value chain.

Commitment To Diversity and Inclusion
Novartis is committed to building an outstanding, inclusive work environment and diverse teams' representative of the patients and communities we serve.
Accessibility and accommodation
Novartis is committed to working with and providing reasonable accommodation to individuals with disabilities. If, because of a medical condition or disability, you need a reasonable accommodation for any part of the recruitment process, or in order to perform the essential functions of a position, please send an e-mail to [email protected] and let us know the nature of your request and your contact information. Please include the job requisition number in your message
Why Novartis: Helping people with disease and their families takes more than innovative science. It takes a community of smart, passionate people like you. Collaborating, supporting and inspiring each other. Combining to achieve breakthroughs that change patients’ lives. Ready to create a brighter future together? https://www.novartis.com/about/strategy/people-and-culture
Join our Novartis Network: Not the right Novartis role for you? Sign up to our talent community to stay connected and learn about suitable career opportunities as soon as they come up: https://talentnetwork.novartis.com/network
Benefits and Rewards: Read our handbook to learn about all the ways we’ll help you thrive personally and professionally: https://www.novartis.com/careers/benefits-rewards


 

Skills Desired

Budget Management, Clinical Research, Clinical Trials, Coaching, Cross-Functional Teamwork, Lifesciences (Inactive), People Management, Risk Management, Risk Monitoring

Skills Required

  • University degree in life science, quantitative science, or business
  • 10+ years of clinical development or clinical operations experience
  • Extensive knowledge of end-to-end clinical development processes, supporting systems, regulations, and the clinical trial lifecycle
  • Experience designing or implementing risk-based quality management processes
  • Experience in process improvement, simplification, and optimization
  • Experience improving quality documentation and managing controlled documents
  • Ability to assess internal and external changes and their impact on processes, systems, and training
  • Ability to collaborate effectively across functions in a complex matrix organization
  • Strategic thinking and ability to contribute to long-term process improvement and operational planning
  • Qualifications or training in shared services, outsourcing, global sourcing, project management, coaching, Six Sigma, Lean, or MBA

Novartis Compensation & Benefits Highlights

The following summarizes recurring compensation and benefits themes identified from responses generated by popular LLMs to common candidate questions about Novartis and has not been reviewed or approved by Novartis.

  • Healthcare Strength Pay and benefits are described as a strong overall package, supported by medical, dental, and vision insurance alongside FSAs/HSAs and disability and life coverage. Mental-health support is reinforced through an employee assistance program with psychological support and a network of mental health first aiders.
  • Retirement Support Retirement support is positioned as a standout element, with an automatic company contribution plus dollar-for-dollar matching in the 401(k). Additional retirement funding is described through an age-based defined contribution program and access to an employee share purchase plan discount.
  • Parental & Family Support Family-related benefits are framed as robust, including a global minimum of paid parental leave for new parents following birth or adoption. Added supports include domestic partner coverage, dependent-care resources, and benefits such as adoption assistance and child/elder care options.

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The Company
HQ: Basel
110,000 Employees
Year Founded: 1996

What We Do

Novartis is an innovative medicines company. Every day, working to reimagine medicine to improve and extend people’s lives so that patients, healthcare professionals and societies are empowered in the face of serious disease. Our medicines reach more than 250 million people worldwide.

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