QA Sr. Manager, Drug Product

The Role

Reporting to the Associate Director, QA Drug Product, the QA Sr. Manager, Drug Product Operations is responsible for coordinating and executing the quality and compliance readiness for a state-of-the-art Drug Product (Fill Finish) cGMP manufacturing facility. This role involves ensuring operational readiness for production of both clinical and commercial drug products while adhering to current GxP, corporate, regulatory and industry best practices.

The role will be required to provide quality oversight of Commissioning, Qualification & Validation (CQV) activities which occur as part of the facility start up,in addition to the support and execution of an end-to-end project quality plan, which includes regulatory inspection readiness.

Upon facility start-up this role will provide end-to-end quality oversight for drug product operations to ensure compliance with cGMPs, company procedures, and regulatory requirements.

The QA Manager will play a crucial role in executing the operational strategy while adhering to regulatory compliance and quality standards. You will be at the forefront of our mission to deliver mRNA therapies to patients worldwide, using your expertise to ensure the smooth operation of our manufacturing processes. Your work will directly contribute to the production of therapies that have the potential to transform the lives of patients.

Heres What Youll Do:

In this role, your responsibilities will include:

• Executing robust operational readiness plans to transition from the construction phase to full-scale production, ensuring all systems and processes are in place for cGMP compliance,

• Execution of a project quality plan, paying key attention to the audit readiness components to ensure a successful pre-approval inspection.

• Assist with the development and implementation of operational and quality systems (i.e. deviation / change management, batch record management, cleaning & disinfection, personnel training, etc.) ensuring Quality 4.0 / Pharma 4.0 principles are embedded into their design.

• Collaborate with cross-functional teams working in a highly matrixed environment to drive decisions and influence outcomes to enable Modernas clinical pipeline

• Routinely identify and escalate project quality risks, and proposed resolution through governance channels, where needed.

• Provide expert guidance and support while managing interfaces with key business stakeholders for quality and operational processes.

• Work to ensure a Right-First-Time and mature quality culture is developed and maintained within the project leading to a successful PAI outcome.

• Support troubleshooting of complex issues encountered during CQV activities. In addition, provide support for CQV deviations and change management teams.

• Ensure timely resolution and/or escalation of quality issues to senior management.

• Ensure adherence to all environmental, health, and safety guidelines, promoting a culture of safety within the operations team,

• Support the development of key performance indicators (KPIs) to measure and report on operational performance, making data-driven decisions to optimize processes,

• Foster a culture of innovation and collaboration, encouraging team members to contribute ideas for process improvements and operational excellence,

• Drive and/or support continuous improvement initiatives to enhance operational efficiency, reduce costs, and improve product quality,

  Heres What Youll Need (Minimum Qualifications):

• Bachelor of Science degree in Engineering, Pharmaceutical Sciences, or a related technology discipline.

A minimum of 8 years of experience in aseptic drug product manufacturing.

Problem-solving mindset with a commitment to quality and safety.

In-depth knowledge of cGMP regulations, aseptic processing, and cleanroom operations.

Strong leadership skills with the ability to develop and motivate a diverse team.

Excellent project management, organizational, and communication skills.

Demonstrated ability to work cross-functionally and manage complex projects with multiple stakeholders, with the ability to convey complex information in an understandable manner to various stakeholders.

Heres What Youll Bring to the Table (Preferred Qualifications):

Proven track record of successful facility start-ups or major operational projects (e.g. Greenfield or Brownfield Projects) within the pharmaceutical industry.

A desire to make an impact as part of a high-growth, transformational company that is Bold, Relentless, Curious, and Collaborative.

Moderna is pleased to provide you and your family with a comprehensive and innovative suite of benefits, including:

About Moderna

Since our founding in 2010, we have aspired to build the leading mRNA technology platform, theinfrastructure 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 peopleare 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.

As we build our company, we have always believed an in-person culture is critical to our success. Moderna champions the significant benefits of in-office collaboration by embracing a 70/30 work model. This 70% in-office structure helps to foster a culture rich in innovation, teamwork, and direct mentorship. Join us in shaping a world where every interaction is an opportunity to learn, contribute and make a meaningful impact.

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 smoke-free, alcohol-free and drug-free work environment.

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 proud to be an equal opportunity workplace and is an affirmative action employer.

Moderna is committed to equal employment opportunity 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. Moderna is an E-Verify Employer in the United States. We also consider qualified applicants regardless of criminal histories, consistent with legal requirements.

Belonging, Inclusion, and Diversity are critical to the success of our company and our impact on society. Were focused on attracting, retaining, developing, and advancing our employees and believe that by cultivating diverse experiences, backgrounds, and ideas, we can provide an environment where every employee is able to contribute their best.

Moderna is committed to offering reasonable accommodations to qualified job applicants with disabilities. Any applicant requiring an accommodation 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 team at leavesandaccommodations@modernatx.com. (EEO/AAP Employer)

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