Manager, GxP Systems

Posted 7 Days Ago
Be an Early Applicant
2 Locations
In-Office
Senior level
Healthtech • Biotech
The Role
Leads GxP validation, qualification, and testing across applications, data platforms, cloud infrastructure, and enterprise systems. Develops risk-based assurance strategies using CSA principles, authors and approves validation deliverables, oversees contractors and partners, supports AI-enabled application assurance, and improves validation methodologies, tools, automation, and audit readiness in collaboration with Digital, Quality, Compliance, and system owners.
Summary Generated by Built In
If you’re interested in this role, please apply in English and include an English version of your Resume/CV.

In this role, you will be responsible for delivering validation, qualification, and testing activities across Moderna’s Digital landscape, including CMC, Digital for Development, Enterprise Platforms, Data Platforms, and Infrastructure. You will apply Computer Software Assurance (CSA) principles and risk-based approaches to plan, develop, execute, review, and approve validation and testing deliverables that ensure GxP applications and infrastructure are appropriately validated and qualified throughout their lifecycle.


You will provide hands-on validation and testing leadership while directing and overseeing contractors and delivery partners to ensure deliverables are completed with the appropriate quality, rigor, and efficiency. You will partner with Digital teams, Compliance, Quality, and system owners while leveraging AI, automation, and modern testing approaches to accelerate delivery, and help define and continuously improve the processes, methodologies, and tools used to validate and qualify applications and infrastructure.


Here’s What You’ll Do

  • Partner with Digital teams, Compliance, Quality, system owners, business process owners, and implementation partners to define validation requirements, resolve issues, and enable timely delivery of GxP technology. 
    • Own and deliver validation, qualification, and testing activities for GxP applications, platforms, data solutions, and infrastructure across Moderna’s Digital landscape. 
    • Develop and execute risk-based validation, qualification, and testing strategies using Computer Software Assurance (CSA) principles and applicable regulatory requirements. 
    • Author, review, and approve key validation deliverables, including GxP applicability and data integrity assessments, validation plans, risk assessments, requirements, test strategies/scripts, traceability, deviations, and validation reports. 
    • Lead the planning, execution, and documentation of testing, ensuring the level of assurance is appropriate for system intended use, complexity, and GxP risk. 
    • Support the validation and assurance of AI-enabled GxP applications, applying risk-based controls and testing approaches appropriate to their intended use. 
    • Apply CSA principles and leverage supplier evidence, automation, AI, and modern testing approaches to increase validation efficiency while maintaining appropriate GxP assurance. 
  • In partnership with Digital, Compliance, and Quality colleagues, define and continuously improve the processes, methodologies, templates, and tools used to validate, qualify, and test GxP applications and infrastructure while supporting audit and inspection readiness. 
  • Provide technical direction and oversight to contractors, consultants, and delivery partners performing validation, qualification, and testing activities, ensuring deliverables meet Moderna quality and compliance expectations. 
  • Additional duties as may be assigned from time to time 

Here’s What You’ll Need (Basic Qualifications)

  • Bachelor’s degree in Computer Science, Engineering, Life Sciences, Information Systems, or a related discipline, with 6+ years of relevant experience in the pharmaceutical, biotechnology, medical device, or other regulated industry; or a Master’s degree with 4+ years of relevant experience.  
  • 4+ years of hands-on experience with GxP computerized systems, including validation, testing, digital quality, or compliance activities.  
  • Demonstrated experience with Computer Software Assurance (CSA), including risk-based assurance, critical thinking, appropriate use of scripted and unscripted testing, and leveraging supplier evidence.  
  • Strong knowledge of applicable regulatory requirements and industry guidance, including 21 CFR Part 11, EU Annex 11, GAMP 5, data integrity principles, and risk-based validation and assurance approaches.  
  • Experience developing, reviewing, and/or approving validation and testing deliverables, including GxP applicability assessments, data integrity assessments, validation plans, risk assessments, requirements, test strategies and scripts, traceability, deviations, and validation reports.  
  • Experience with SaaS/cloud-based GxP applications and evaluating and leveraging supplier/vendor documentation and testing evidence.  
  • Working knowledge of SDLC, change management, and release management processes and their application to regulated computerized systems.  
  • Demonstrated experience leading and overseeing contractors, consultants, or external service providers, including assigning work, reviewing deliverables, providing technical direction, and ensuring work meets quality, compliance, and delivery expectations.  
  • Demonstrated ability to lead cross-functional validation and testing activities and influence without direct authority, partnering effectively with Quality, Digital/IT, business process owners, system owners, vendors, and implementation partners.  
  • Strong written and verbal communication skills, including the ability to translate regulatory and quality requirements into pragmatic system, assurance, and testing requirements. 

Here’s What You’ll Bring to the Table (Preferred Qualifications) 

  • Experience validating or assuring artificial intelligence (AI), machine learning (ML), or AI-enabled applications in a GxP environment, including applying risk-based approaches to intended use, data, model performance, testing, human oversight, and ongoing system changes. 
  • Experience leveraging AI, automation, or digital tools to improve or accelerate validation and testing activities, such as requirements development, risk assessments, test generation, test execution, traceability, or documentation review. 
  • Experience developing or improving validation, qualification, and testing methodologies, processes, templates, and tools to increase efficiency while maintaining appropriate GxP compliance and control. 
  • Experience validating or qualifying solutions across multiple technology domains, such as enterprise applications, data platforms, cloud infrastructure, laboratory/manufacturing systems, or development platforms. 
  • Demonstrated ability to identify opportunities to simplify and modernize traditional validation approaches through risk-based assurance, automation, supplier leveraging, and new technologies. 
  • A desire to make an impact as part of a high-growth, transformational company that is Bold, Relentless, Curious, and Collaborative. 

Pay & Benefits


At Moderna, we believe that when you feel your best, you can do your best work.  That’s why our benefits and well-being resources are designed to support you—at work, at home, and everywhere in between.

  • Competitive healthcare, plus voluntary benefit programs to support your unique needs
  • A holistic approach to well-being with access to fitness, mindfulness, and mental health support
  • Family building benefits, including fertility, adoption, and surrogacy support
  • Generous paid time off, including vacation, bank holidays, volunteer days, sabbatical, global recharge days, and a discretionary year-end shutdown
  • Savings and investments to help you plan for the future
  • Location-specific perks and extras

The benefits offered may vary depending on the nature of your employment with Moderna and the country where you work.


About Moderna

Since our founding in 2010, we have aspired to build the leading mRNA technology platform, the infrastructure to reimagine how medicines are created and delivered, and a world-class team. We believe in giving our people a platform to change medicine and an opportunity to change the world.  


By living our mission, values, and mindsets every day, our people are the driving force behind our scientific progress and our culture. Together, we are creating a culture of belonging and building an organization that cares deeply for our patients, our employees, the environment, and our communities. 


We are proud to have been recognized as a Science Magazine Top Biopharma Employer, a Fast Company Best Workplace for Innovators, and a Great Place to Work in the U.S. 

If you want to make a difference and join a team that is changing the future of medicine, we invite you to visit modernatx.com/careers to learn more about our current opportunities. 


Moderna is a place where everyone can grow. If you meet the Basic Qualifications for the role and you would be excited to contribute to our mission every day, please apply! 


Moderna is committed to equal opportunity in employment and non-discrimination for all employees and qualified applicants without regard to a person's race, color, sex, gender identity or expression, age, religion, national origin, ancestry or citizenship, ethnicity, disability, military or protected veteran status, genetic information, sexual orientation, marital or familial status, or any other personal characteristic protected under applicable law. We consider qualified applicants regardless of criminal histories, consistent with legal requirements. 


We’re focused on attracting, retaining, developing, and advancing our employees. By cultivating a workplace that values diverse experiences, backgrounds, and ideas, we create an environment where every employee can contribute their best. 


Moderna is committed to offering reasonable accommodation or adjustments to qualified job applicants with disabilities. Any applicant requiring an accommodation or adjustment in connection with the hiring process and/or to perform the essential functions of the position for which the applicant has applied should contact the Accommodations and Adjustments team at [email protected]. 

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Skills Required

  • Bachelor's degree in Computer Science, Engineering, Life Sciences, Information Systems, or a related discipline, plus 6+ years of relevant regulated-industry experience; or a master's degree plus 4+ years of relevant experience
  • 4+ years of hands-on experience with GxP computerized systems, validation, testing, digital quality, or compliance activities
  • Experience with Computer Software Assurance, risk-based assurance, scripted and unscripted testing, critical thinking, and supplier evidence
  • Knowledge of 21 CFR Part 11, EU Annex 11, GAMP 5, data integrity principles, and risk-based validation approaches
  • Experience developing, reviewing, or approving GxP applicability assessments, data integrity assessments, validation plans, risk assessments, requirements, test strategies, scripts, traceability, deviations, and validation reports
  • Experience with SaaS or cloud-based GxP applications and supplier or vendor documentation and testing evidence
  • Working knowledge of SDLC, change management, and release management for regulated computerized systems
  • Experience leading and overseeing contractors, consultants, or external service providers
  • Ability to lead cross-functional validation and testing activities and influence without direct authority
  • Strong written and verbal communication skills, including translating regulatory and quality requirements into system and testing requirements
  • Experience validating or assuring AI, machine learning, or AI-enabled applications in a GxP environment
  • Experience using AI, automation, or digital tools to improve validation and testing
  • Experience improving validation methodologies, processes, templates, and tools
  • Experience validating solutions across enterprise applications, data platforms, cloud infrastructure, laboratory or manufacturing systems, or development platforms
  • Ability to modernize validation through risk-based assurance, automation, supplier evidence, and new technologies

Moderna Compensation & Benefits Highlights

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

  • Fair & Transparent Compensation — Pay is commonly characterized as fair, competitive, and a financial positive, with base pay complemented by bonus and other cash elements.
  • Equity Value & Accessibility — Long-term rewards commonly include stock options and RSUs, positioning equity as a meaningful part of overall compensation rather than an occasional add-on.
  • Parental & Family Support — Family-related support is extensive, including fully paid parental leave, paid family caregiver leave, family-building benefits such as fertility/adoption/surrogacy support, and childcare resources.

Moderna Insights

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The Company
HQ: Cambridge, Massachusetts
6,848 Employees
Year Founded: 2010

What We Do

At Moderna, we believe messenger RNA, or mRNA, is the “software of life.” Every cell in the body uses mRNA to provide real-time instructions to make the proteins necessary to drive all aspects of biology, including in human health and disease. Given its essential role, we believe mRNA could be used to create a new category of medicines with significant potential to improve the lives of patients. We are pioneering a new class of medicines made of messenger RNA, or mRNA. The potential implications of using mRNA as a drug are significant and far-reaching and could meaningfully improve how medicines are discovered, developed and manufactured. To learn more, visit www.modernatx.com. This Moderna page is not the appropriate place to report adverse events (side-effects) for any products. If you are or someone you know is experiencing a side effect, please reach out to your healthcare professional. Moderna is continuously monitoring the safety of its products. We encourage you to report any side effects directly to us at 1‑866‑MODERNA (1‑866‑663‑3762).

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