Sr. Engineer I, MS&T, Small Molecules

vor 1 Monat

Basel, Schweiz Moderna Vollzeit

The Role
Joining Moderna offers the unique opportunity to be part of a pioneering team that's revolutionizing medicine through mRNA technology with a diverse pipeline of development programs across various diseases. As an employee, you'll be part of a continually growing organization working alongside exceptional colleagues and strategic partners worldwide, contributing to global health initiatives. Moderna's commitment to advancing the technological frontier of mRNA medicines ensures a challenging and rewarding career experience with the potential to make a significant impact on patients' lives worldwide.

Moderna is solidifying its footprint in Basel, the vibrant hub of pharmaceutical innovation in Switzerland, to further our mission of delivering the greatest possible impact to people through mRNA medicines. As we grow our international operations and commercial activities in Basel, we invite global talents to join us in this exciting journey of transforming medicine and impacting lives worldwide.

Join Moderna’s Manufacturing Science and Technology (MST) team as a Sr. Engineer I, External DS MS&T (Chemistry), where you will play a pivotal role in ensuring the robust production of custom small molecules—lipids and nucleotides—at Contract Manufacturing Organizations (CMOs) across the USA and Europe. In this critical role, you’ll support our groundbreaking mRNA platform for both Clinical and Commercial cGMP Manufacturing. You will collaborate with internal teams and CMOs to navigate the complexities of technology transfer and provide technical support, ensuring flawless execution and adherence to Moderna’s high standards. This is a unique opportunity to contribute significantly to the future of medicine at Moderna.

Here’s What You’ll Do

Your key responsibilities will be:

  1. Leading technology transfer activities for clinical and commercial products into CMOs.
  2. Providing comprehensive technical support for cGMP manufacturing at CMOs, including authoring technology transfer documents and supporting change controls, deviations, and the closure of manufacturing investigations.
  3. Analyzing manufacturing performance through data review and analyses, authoring manufacturing summary reports, and establishing and maintaining data repositories.
  4. Leading cross-functional troubleshooting and operational improvements for manufacturing processes and equipment.
  5. Authoring and executing protocols that support process characterization and equipment scale-up in cGMP Manufacturing.
  6. Maintaining alignment with other global manufacturing sites through shared knowledge, manufacturing data, and collaborative problem-solving.

Your responsibilities will also include:
  1. Managing project deliverables in a fast-paced, dynamic environment.
  2. Collaborating effectively within a cross-functional matrix, contributing to shared goals and strategies.
  3. Adapting to new technical challenges and opportunities as they arise.

The key Moderna Mindsets you’ll need to succeed in the role:
  1. We digitize everywhere possible: In this role, you will need to leverage digital tools to establish and maintain data repositories, enhancing data-driven decision-making and operational efficiency across global manufacturing sites.
  2. We prioritize the platform: You will focus on the robustness of Moderna’s mRNA platform by ensuring reliable production standards across all CMO engagements, contributing directly to Moderna’s long-term impact in advancing mRNA technology.

Here’s What You’ll Need (Basic Qualifications)
  1. BS (8+ years), MS (6+ years) or PhD (2+) in Chemical Engineering or related scientific disciplines with direct industry experience within small molecule production.
  2. Demonstrated experience with Good Manufacturing Practice (GMP) in a regulated environment, ensuring compliance with quality and industry regulatory requirements.

Here’s What You’ll Bring to the Table (Preferred Qualifications)
  1. Ability to manage projects in a fast-paced environment.
  2. Ability to effectively collaborate in a dynamic, cross-functional matrix environment.
  3. Ability to adapt to new and challenging technical opportunities.
  4. Experience in providing technical support to cGMP manufacturing organizations.
  5. A desire to make an impact as part of a high-growth, transformational company that is Bold, Relentless, Curious, and Collaborative.

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.

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 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. #J-18808-Ljbffr

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