Manufacturing Technician

ZipRecruiter; England; On-site; GBP 30,000 - 45,000; Full time

Job summary

Join a global leader in mRNA innovation as a Manufacturing Associate. This hands-on role involves operating advanced manufacturing equipment, ensuring compliance with cGMP standards, and contributing to the production of life-saving vaccines. If you have 3+ years in a GMP environment and a degree in Pharmaceutical Production Technology, we want to hear from you.

Qualifications

• 3+ years of experience in a GMP manufacturing environment.
• Strong technical skills and scientific mindset.
• Familiarity with regulatory guidelines and audit preparation.

Responsibilities

• Operate production equipment in a cleanroom environment.
• Collaborate with QA teams for batch documentation.
• Troubleshoot equipment and maintain smooth operations.

Skills

Technical skills

Communication

Collaboration

Problem-solving

Attention to detail

Education

Degree in Pharmaceutical Production Technology or related field

Job description

Job Description

Join a Global Leader in mRNA Innovation – Now Hiring: Manufacturing Associate

About the Client

Our client is at the forefront of mRNA technology, driving innovation in vaccine and therapeutic development. With a growing global presence and a commitment to public health, they are establishing a cutting-edge research, development, and manufacturing facility dedicated to onshore mRNA vaccine production for respiratory diseases.

This is a unique opportunity to be part of a transformative initiative that will shape the future of healthcare in the UK and beyond.

The Opportunity:

Manufacturing Associate – mRNA Vaccine Production

We are seeking a skilled and digitally proficient Manufacturing Associate to join a high-tech production unit. In this hands-on role, you’ll operate advanced manufacturing equipment in compliance with cGMP and health & safety standards, contributing directly to the production of life-saving vaccines.

What You’ll Do

• Operate production equipment in a cleanroom environment, ensuring compliance with cGMP and safety protocols.
• Collaborate with QA teams to support timely batch documentation and release.
• Participate in investigations and CAPA processes to resolve deviations.
• Troubleshoot equipment and digital systems to maintain smooth operations.
• Perform routine maintenance tasks and keep training records up to date.
• Contribute to continuous improvement initiatives and cross-functional projects.

What You’ll Bring

• 3+ years of experience in a GMP manufacturing environment.
• Degree in Pharmaceutical Production Technology or a related field.
• Strong technical skills and a scientific mindset.
• Experience with filtration, chromatography, and cold chain management is a plus.
• Familiarity with regulatory guidelines and audit preparation.
• Excellent communication, organization, and collaboration skills.
• A proactive, detail-oriented approach with a passion for innovation.

Work Schedule This is a site-based role at the client’s facility. While standard hours apply outside of campaigns, during manufacturing campaigns you’ll work a 2-2-3 (Panama) shift pattern:

• 12-hour shifts
• 2 days on, 2 days off, 3 days on – rotating every 28 days

About Planet Pharma:

Planet Pharma is an American parented Employment Business/Agency that provides global staffing services with its head-quarters in Chicago and our EMEA regional office located in Central London. We have invested significantly in creating a robust international platform that enables us to work compliantly in 30+ countries with a current network of 2500+ active contractors globally as well as a very strong permanent / direct hire recruitment offering.

Our specialist knowledge and close relationships with our clients and the wider industry really makes us unique in our field. Just recently we were recognised by FORBES as the 17th best professional staffing firm, and have won multiple awards from industry accredited bodies for our commitment to excellence and service delivery. We have extensive functional expertise including: Regulatory Affairs, Pharmacovigilance, QA, QC, Submissions experts, Clinical development, Quality, Biostatistics, and Medical Affairs / Writing.

We are an equal opportunities Recruitment Business and Agency. We welcome applications from all suitably qualified candidates regardless of their , , , /belief, or .

www.planet-pharma.com