Manufacturing Associate

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

Job summary

A leading biopharmaceutical company seeks a Manufacturing Associate in Crawley to support innovative vaccine production. In this role, you will ensure compliance with GMP standards and contribute to operational excellence through advanced production equipment monitoring and quality assurance processes.

Qualifications

• 1+ years of experience in a GMP manufacturing environment.
• Comfort working in a fast-paced, technology-driven environment.
• Experience in filtration, chromatography, cold chain management is a plus.

Responsibilities

• Operate and monitor biopharmaceutical production equipment in compliance with GMP standards.
• Perform routine equipment maintenance, including lubrication and mechanical checks.
• Participate in root cause analysis and continuous improvement initiatives.

Skills

Attention to detail

Problem-solving

Education

Degree in pharmaceutical production technology or equivalent

Job description

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Manufacturing Associate, crawley, west sussex

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Client:

Planet Pharma

Location:

crawley, west sussex, United Kingdom

Job Category:

Other

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EU work permit required:

Yes

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Job Views:

2

Posted:

06.06.2025

Expiry Date:

21.07.2025

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Job Description:

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.