(Fixed Term) Manufacturing Associate I

Moderna Therapeutics; Oxford; Hybrid; GBP 30,000 - 46,000; Full time

Benefits offered by this job

Competitive healthcare

Family building benefits

Generous paid time off

Global recharge days

Job summary

Moderna Therapeutics in the United Kingdom (Oxford) is seeking a GMP manufacturing operator to join our mRNA vaccine production team. You will operate production equipment, follow cGMP standards, and document manufacturing activities to support timely batch disposition.

This hands-on position requires precise execution and collaboration with QA to ensure quality and compliance. The role emphasizes safe practices, rigorous housekeeping, and ongoing training in a fast-paced, matrix-organized

Qualifications

• 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.
• Attention to detail while executing multiple tasks with minimal supervision.
• Demonstrated commitment to Moderna's values of Bold, Collaborative, Curious, and Relentless.

Responsibilities

• Operate manufacturing equipment for mRNA vaccine production per cGMP and SOPs.
• Maintain safe working habits and comply with health, safety, and environmental procedures.
• Follow gowning procedures and keep an inspection-ready environment.
• Execute operations ensuring top quality, compliance, and efficiency.
• Collaborate with Quality Assurance to document production for batch disposition.
• Assist in investigations of deviations via RCA and support CAPA actions.
• Contribute to incident investigations and improve operational performance.
• Triage routine equipment and digital system issues and escalate when needed.
• Maintain training records and documentation; participate in continuous improvement.
• Support off-hours work and cross-functional projects in a fast-paced setting.

Skills

GMP manufacturing experience

Collaboration

Attention to detail

Communication

Education

University degree in pharmaceutical production technology or equivalent

Tools

Filtration

Chromatography

Cold chain management

Job description

**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's What 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 escalate 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.**The key Moderna Mindsets you'll need to succeed in the role:*** 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.**Here’s What You’ll Bring to the Table:*** 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 commitment to Moderna's values of Bold, Collaborative, Curious, and Relentless, embodying these values in the workplace**Our Working Model**As we build our company, we have always believed that an in-person culture is critical to our success. This role is 100% onsite, reflecting the importance of being physically present to support the work, collaborate closely with colleagues, and contribute to our site-based operations.Working onsite enables real-time collaboration, strong team connections, direct mentorship, and the hands-on partnership needed to deliver our mission. Join us in shaping a world where every interaction is an opportunity to learn, contribute, and make a meaningful impact. Moderna is a smoke-free, alcohol-free, and drug-free work environment. **Pay & Benefits** **At Moderna, we believe that when you feel your best, you can do your best work.****That’s why our benefits and well-being resources are designed to support you—at work, at home, and everywhere in between.*** Competitive healthcare, plus voluntary benefit programs to support your unique needs* A holistic approach to well-being with access to fitness, mindfulness, and mental health support* Family building benefits, including fertility, adoption, and surrogacy support* Generous paid time off, including vacation, bank holidays, volunteer days, sabbatical, global recharge days, and a discretionary year-end shutdown* Savings and investments to help you plan for the future* Location-specific perks and extras