Manufacturing Associate

JR United Kingdom; Milton Keynes; On-site; GBP 25,000 - 35,000; Full time

Job summary

An innovative biopharmaceutical company is hiring Manufacturing Associates in Milton Keynes to support vaccine production. The role involves operating advanced production equipment, ensuring GMP compliance, and participating in quality assurance and process optimization. Ideal candidates have a degree in pharmaceutical production technology and experience in a GMP environment.

Qualifications

• 1+ years of experience in a GMP manufacturing environment.
• Experience in filtration, chromatography, cold chain management is a plus.
• Familiarity with audit/inspection preparation and regulatory compliance.

Responsibilities

• Operate and monitor biopharmaceutical production equipment in compliance with GMP standards.
• Accurately document manufacturing processes for batch disposition and regulatory compliance.
• Engage in continuous improvement initiatives, optimizing production workflows.

Skills

Attention to detail

Problem solving

Adaptability

Education

Degree in pharmaceutical production technology or equivalent

Job description

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Planet Pharma are working with an innovative biopharmaceutical company, who are seeking Manufacturing Associates to contribute to cutting-edge vaccine production, ensuring compliance with GMP and safety regulations, while working in a highly automated, technology-driven environment. This is a chance to be part of a mission-driven team dedicated to global healthcare advancement.

The Role

As a Manufacturing Associate, you will operate and monitor advanced production equipment, ensuring efficient and compliant manufacturing. You’ll play a crucial role in batch quality assurance, regulatory adherence, and digital process optimization.

Key Responsibilities

• Operate and monitor biopharmaceutical production equipment in compliance with GMP standards.
• Maintain a clean, safe, and compliant workspace, adhering to gowning and housekeeping protocols.
• Accurately document manufacturing processes for batch disposition and regulatory compliance.
• Perform routine equipment maintenance, including lubrication, filter changes, and mechanical checks.
• Troubleshoot equipment and digital systems, ensuring operational efficiency.
• Work collaboratively with QA, cross-functional teams, and leadership to meet production KPIs.
• Engage in continuous improvement initiatives, optimizing production workflows.
• Participate in root cause analysis (RCA), corrective actions (CAPA), and incident investigations.
• Leverage digital tools and automation to drive operational excellence.

What You Bring

• 1+ years of experience in a GMP manufacturing environment.
• Degree in pharmaceutical production technology or equivalent.
• Comfort working in a fast-paced, technology-driven environment requiring adaptability.
• Experience in filtration, chromatography, cold chain management (a plus).
• Strong attention to detail, ability to prioritize tasks, and problem-solving mindset.
• Familiarity with audit/inspection preparation and regulatory compliance.