Manufacturing Associate

JR United Kingdom; Bolton; On-site; GBP 25,000 - 33,000; Full time

Job summary

A leading biopharmaceutical company is seeking a Manufacturing Associate for vaccine production in Bolton. The role involves operating advanced production equipment and ensuring compliance with GMP standards. Candidates should have experience in a GMP environment and a relevant degree, along with strong problem-solving and adaptability skills.

Qualifications

• At least 1 year of experience in a GMP manufacturing environment.
• Ability to work in a fast-paced, technology-driven environment.
• Experience in filtration and chromatography preferred.

Responsibilities

• Operate and monitor biopharmaceutical production equipment in compliance with GMP standards.
• Document manufacturing processes accurately for regulatory compliance.
• Engage in continuous improvement initiatives to optimize workflows.

Skills

Attention to detail

Problem-solving

Adaptability

Education

Degree in pharmaceutical production technology

Tools

Digital tools and automation

Job description

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Manufacturing Associate, Bolton, Greater Manchester

Client: Planet Pharma

Location: Bolton, Greater Manchester, United Kingdom

Job Category: Other

EU work permit required: Yes

Job Views:

2

Posted:

06.06.2025

Expiry Date:

21.07.2025

Job Description:

Planet Pharma is working with an innovative biopharmaceutical company seeking Manufacturing Associates to contribute to cutting-edge vaccine production, ensuring compliance with GMP and safety regulations, in a highly automated, technology-driven environment. This role offers an opportunity to be part of a 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 will 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, following gowning and housekeeping protocols.
• Document manufacturing processes accurately for batch disposition and regulatory compliance.
• Perform routine equipment maintenance, including lubrication, filter changes, and mechanical checks.
• Troubleshoot equipment and digital systems to ensure operational efficiency.
• Collaborate with QA, cross-functional teams, and leadership to meet production KPIs.
• Engage in continuous improvement initiatives to optimize workflows.
• Participate in root cause analysis (RCA), corrective actions (CAPA), and incident investigations.
• Utilize digital tools and automation to enhance operational performance.

What You Bring

• At least 1 year of experience in a GMP manufacturing environment.
• Degree in pharmaceutical production technology or an equivalent qualification.
• Ability to work effectively in a fast-paced, technology-driven environment requiring adaptability.
• Experience in filtration, chromatography, cold chain management (preferred).
• Strong attention to detail, prioritization skills, and problem-solving abilities.
• Familiarity with audit/inspection preparation and regulatory compliance.