Latest mRNA Technology Jobs

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(Fixed Term) Analyst, Quality Control, Microbiology

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,...

Moderna Oxford, United Kingdom
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(Fixed Term) Analyst, Quality Control, Microbiology

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,...

Moderna Gargrave, BD23 3RZ, United Kingdom
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(Fixed Term) Senior Research Associate, Clinical Biomarker Laboratory, Flow Cytometry

This role involves working as a technical expert in the Clinical Flow Cytometry group at Moderna's Harwell facility, generating high-quality clinical trial data through advanced flow cytometry assays. Responsibilities include executing clinical sample testing, conducting immune profiling, and ensuring data integrity and compliance with GCLP standards.

Moderna Oxford, United Kingdom
On-site Contract
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Senior Manager - Engineering & Maintenance

This role involves providing technical leadership for engineering and maintenance systems at Moderna’s new biotech facility in Harwell, Oxford. The Senior Manager will oversee critical infrastructure, utilities, and vendor performance across R&D and manufacturing environments, ensuring operational reliability, compliance, and continuous improvement. With a strong focus on GMP standards and digital transformation—including exposure to AI-enabled tools—this position plays a central role in supporting mRNA vaccine production and scaling advanced engineering practices within a high-impact, on-site setting.

Moderna Oxford, United Kingdom
On-site Permanent
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(Fixed Term) Senior Research Associate, Clinical Biomarker Laboratory, Flow Cytometry

This role involves working as a technical expert in the Clinical Flow Cytometry group at Moderna's Harwell facility, focusing on generating high-quality clinical trial data through advanced flow cytometry assays. Responsibilities include executing clinical sample testing, conducting immune profiling, and ensuring data integrity and compliance with GCLP standards.

On-site Contract
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Senior Manager - Engineering & Maintenance

This role involves leading engineering and maintenance excellence at Moderna’s new mRNA manufacturing site in Harwell, UK. The Senior Manager will provide technical oversight of facility systems, manage vendor performance, and drive continuous improvement across R&D and manufacturing environments. With a focus on compliance, reliability, and digital innovation—including AI-enabled tools—this position plays a key technical and strategic role in supporting life-saving vaccine production.

On-site Permanent
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(Fixed Term) Warehouse Specialist

In this hands-on role, you will ensure seamless warehouse and logistics support within a 24/7 GMP environment at Moderna’s UK manufacturing facility. You will manage inventory, coordinate deliveries, and maintain compliance with safety and operational standards, directly supporting mRNA vaccine production.

Moderna Oxford, United Kingdom
On-site Permanent Shift-work
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(Fixed Term) Warehouse Specialist

This role involves operating in a 24/7 GMP environment at Moderna’s UK manufacturing facility, ensuring seamless warehouse and logistics support. Responsibilities include managing inventory, verifying deliveries, coordinating shipments, and maintaining compliance with safety and operational standards.

On-site Contract Shift-work
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(Fixed Term) Manufacturing Associate I

The Manufacturing Associate will operate production equipment for mRNA vaccines, ensuring compliance with cGMP and safety regulations. Responsibilities include maintaining documentation, troubleshooting equipment, and participating in continuous improvement projects in a fast-paced, team-oriented environment.

Moderna Oxford, United Kingdom
On-site Temporary
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Fixed Term Manufacturing Associate II

This role involves operating production equipment for mRNA vaccines, adhering to cGMP and safety regulations, and participating in continuous improvement initiatives. The candidate will work closely with QA teams, troubleshoot equipment issues, and maintain meticulous documentation in a fast-paced, technologically advanced environment.

Moderna Oxford, United Kingdom
On-site Temporary
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(Fixed Term) Manufacturing Associate I

The Manufacturing Associate I will operate production equipment for mRNA vaccines, ensuring compliance with cGMP and safety regulations. They will work in a highly technological environment, collaborating with QA teams, troubleshooting issues, and participating in continuous improvement projects.

On-site Temporary
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Fixed Term Manufacturing Associate II

This role involves operating production equipment for mRNA vaccines, adhering to cGMP and safety regulations, and participating in continuous improvement initiatives. The candidate will work closely with QA, troubleshoot equipment issues, and maintain meticulous documentation in a fast-paced, team-oriented environment.

On-site Temporary
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Associate Director, CMC Regulatory Science, International

This role involves developing and implementing CMC regulatory strategies for global submissions, providing guidance on regulatory CMC aspects, and ensuring compliance with health authority guidelines. The candidate will support multiple programs in various therapeutic areas, including vaccines, oncology, and rare diseases, and work closely with manufacturing and quality teams.

Moderna London, United Kingdom
On-site Permanent
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Associate Director, CMC Regulatory Science, International

This role involves developing and implementing CMC regulatory strategies for global submissions, providing guidance on regulatory CMC aspects, and ensuring compliance with health authority guidelines. The candidate will support multiple programs in various therapeutic areas, including vaccines, oncology, and rare diseases, and contribute to the development of regulatory processes and procedures.

On-site Permanent
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Manager, Global Regulatory Science CTA

This role involves leading the operational execution of Clinical Trial Applications (CTAs) globally, outside the US, with a focus on the UK regulatory landscape. Responsibilities include managing CTA submissions, ensuring regulatory compliance, coordinating with CROs, and leveraging advanced digital tools to enhance submission efficiency.

Moderna Poland
On-site Permanent