工作类型: Full-time

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工作内容

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.

In Basel, Switzerland, Moderna is expanding its international presence, integrating cutting-edge biotechnology within the vibrant hub of pharmaceutical innovation. We invite professionals to join us in Basel, contributing to our mission of delivering groundbreaking mRNA medicines and impacting lives worldwide.

Moderna is seeking an experienced Associate Director for CMC Regulatory Affairs-International at our Basel site. This pivotal role involves leading regulatory activities, developing CMC strategies for international submissions, ensuring compliance, and guiding product development projects. You will be at the forefront of preparing and overseeing critical regulatory documentation, directly contributing to the development of transformative medicines for patients.

Here’s What You’ll Do:

Within 3 Months, You Will…

  • Develop and implement effective CMC regulatory strategies for international submissions.
  • Start reviewing documents for submission-readiness, ensuring conformity with health authority guidelines.
  • Begin providing regulatory guidance to manufacturing and quality teams.
Within 6 Months, You Will…

  • Lead regulatory CMC discussions and interactions with health authorities.
  • Enhance regulatory processes and procedures supporting CMC components.
  • Support the creation and maintenance of CMC submission templates.
Within 12 Months, You Will:

  • Provide comprehensive CMC regulatory guidance for various therapeutic areas.
  • Oversee multiple programs, evaluating CMC change controls and their impact on internal programs.
  • Lead and support all regulatory activities, delivering high-quality CMC sections of regulatory documentation.
Here’s What You’ll Bring to the Table:

  • BS in Pharmaceutics, Chemistry, Chemical Engineering, or closely related field is required.
  • MS degree in Pharmaceutics, Chemistry, Chemical Engineering, or closely related field is desirable
  • 10+ years of experience in the pharmaceutical/biotech industry, manufacturing and/or analytical focus
  • 8+ years of experience in Biologics focused Regulatory CMC
  • Multidisciplinary focus on certain therapeutic areas (vaccines, oncology and/or rare diseases)
  • Strong knowledge of current EU and ROW regulations
  • Strong knowledge of Cgmp
  • Strong experience with CTD format and content regulatory filings
  • Exceptional written and oral communication
Moderna offers personalized benefit programs and well-being resources as unique as our global workforce so employees can do their best work.

We recognize and appreciate your diverse needs and interests and do our best to support you at work and at home with:

  • Quality healthcare and insurance benefits
  • Lifestyle Spending Accounts to create your own pathway to well-being
  • Free premium access to fitness, nutrition, and mindfulness classes
  • Family planning and adoption benefits
  • Generous paid time off, including vacation, bank holidays, volunteer days, sabbatical, and a discretionary year-end shutdown
  • Educational resources
  • Savings and investments
  • 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 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. We’re 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 make a request to the Talent Acquisition Partner or contact the Accommodations team at leavesandaccommodations@modernatx.com. (EEO/AAP Employer)

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最后期限: 23-05-2024

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