Principal Research Associate Ms&T Dp

3 days ago

Melbourne, Victoria, Australia Moderna Therapeutics Full time

Principal Research Associate MS&T DP - Validation page is loaded
Principal Research Associate MS&T DP - Validation
Apply locations Melbourne - Australia Drug Manufacturing time type Full time posted on Posted Yesterday job requisition id R17764
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 presence in Melbourne, a city at the forefront of Australia's biotech industry. Our Melbourne office focuses on commercial operations, ensuring the delivery of our innovative products to the Australian market. We're inviting international professionals to join us in our mission of delivering the greatest possible impact to people through mRNA medicines.
As a Principal Research Associate, MS&T - Validation, you will be responsible for establishing Drug Product (DP) MS&T activities at our Clayton, Australia site (MTC-M). Reporting to the MS&T Drug Product Site Lead, you will serve as a technical specialist ensuring robust validation practices, technology transfers, continued process verifications, investigations, and change management in support of a new drug product manufacturing line. Your expertise will drive the development of compliant, high-quality systems and processes critical to delivering mRNA products for local and export markets. As a senior team member, you will champion quality culture and contribute to the site's technical leadership.
Here's What You'll Do:
Your key responsibilities will be:
Lead formulation, fill/finish, visual inspection, packaging, and related process validation and tech

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