Manufacturing Associate
Listed on 2026-09-12
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Manufacturing / Production
Production QC/QA, Regulatory Compliance Specialist, Manufacturing & Industrial Operations, Pharmaceutical Manufacturing
The Role:
Joining Moderna means advancing mRNA science to transform medicine. Work with exceptional global teams on a broad pipeline and build a career that makes a real difference for patients.
Join our mRNA vaccine production team and play a pivotal role in delivering safe, effective vaccines to patients around the world. This is an opportunity to work in a highly digital, technology-driven manufacturing environment where scientific thinking, operational excellence, and continuous innovation come together. You'll help operate advanced production systems, contribute to continuous improvement initiatives, and have the opportunity to work alongside cutting‑edge digital and Generative AI‑enabled technologies that support the future of manufacturing.
Here'sWhat You'll Do:
- Operate manufacturing equipment supporting mRNA vaccine production in accordance with current Good Manufacturing Practices (cGMP), approved Standard Operating Procedures (SOPs), and manufacturing documentation.
- Practice safe working habits while adhering to Moderna's health, safety, and environmental procedures and guidelines.
- Follow gowning procedures and maintain housekeeping standards within your assigned manufacturing area to ensure a compliant, safe, and inspection‑ready environment.
- Execute manufacturing operations while maintaining the highest standards of quality, compliance, and operational excellence.
- Partner closely with Quality Assurance colleagues to complete production documentation required to support the timely disposition of commercial batches.
- Participate in investigations of manufacturing deviations through Root Cause Analysis (RCA) and support the implementation of Corrective and Preventive Actions (CAPA).
- Contribute to incident investigations and associated RCA and CAPA activities to strengthen operational performance and compliance.
- Apply operational performance tools while working collaboratively with the team to achieve operational KPI objectives aligned with corporate goals and commercial demand.
- Rapidly respond to and troubleshoot routine equipment, manufacturing process, and digital system issues.
- Proactively identify and elevate compliance, quality, health, or safety concerns to the Team Lead or Supervisor.
- Maintain accurate and up‑to‑date training records and associated documentation.
- Perform routine basic equipment maintenance, including lubrication, basic mechanical checks, and filter changes using hand tools.
- Participate in multiple projects and continuous improvement initiatives within a fast‑paced manufacturing environment.
- Collaborate effectively across cross‑functional teams within a dynamic matrix organisation.
- Demonstrate flexibility to support off‑hours work and overtime when business needs require.
- Continuously build technical capability through rapid learning of new mRNA manufacturing technologies and evolving digital tools.
- We obsess over learning. We don’t have to be the smartest we have to learn the fastest.
- We behave like owners. The solutions we’re building go beyond any job description.
- 1+ years of experience in a GMP manufacturing environment
- A university degree with a specialization in pharmaceutical production technology or equivalent
- Experience with filtration and chromatography, and cold chain management a plus
- Experience in audit / inspection preparation, understanding Health authority and regulatory guidelines
- Ability to collaborate fluidly with peers, leadership and cross‑functional support groups required
- Excellent written, oral communication, and organizational skills required.
- Ability to maintain attention to detail while executing multiple tasks with minimal supervision
- Demonstrated…
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