Process Operator

Russell Taylor Group; England; On-site; GBP 31,000; Full time

Job summary

A leading pharmaceutical company is seeking a Process Operator in Cheshire. This role involves preparing and assembling IV bags, maintaining compliance with GMP standards, and coordinating with cleanroom teams. The successful candidate will receive full training and has the opportunity to build a long-term career in a growing industry with a competitive salary and benefits including a bonus.

Benefits

Excellent starting salary

Structured pay increase after training

Full training and professional development

Opportunities for career growth

Qualifications

• Experience in a cleanroom or pharmaceutical environment is preferred.
• Training will be provided for candidates without prior experience.
• Knowledge of GMP and the ability to follow strict procedures are important.

Responsibilities

• Prepare and organise materials for aseptic compounding.
• Assemble, label, and package IV bags following GMP.
• Complete documentation accurately to maintain compliance.
• Coordinate with cleanroom teams to ensure material flow.
• Maintain cleanliness of work areas and equipment.
• Monitor stock levels and ensure timely replenishment.

Skills

Experience in cleanroom or pharmaceutical environment

Knowledge of GMP

Effective communication skills

Detail-oriented approach

Job description

Vacancy Title: Process Operator

Contract Type: Permanent

Location: Cheshire (Runcorn)

Industry: Manufacturing – Pharmaceutical

Salary: £30,296 per annum + £930 annual bonus

Start Date: 2025-11-26

Shift Pattern: Monday to Friday, rotating 6:00 am–2:00 pm and 2:00 pm–10:00 pm

Note: Own transport required due to shift times and site location.

What You'll Be Doing:

• Prepare, sanitise, and organise components, consumables, and materials required for aseptic compounding, ensuring timely and compliant transfer into the cleanroom.
• Accurately assemble, label, and package patient‑specific IV bags and other compounded products following GMP and product traceability requirements.
• Complete batch documentation, order forms, and material movement logs with a high level of accuracy to maintain full compliance and data integrity.
• Coordinate with cleanroom teams to ensure efficient flow of materials, prioritisation of patient orders, and availability of required items.
• Maintain cleanliness and readiness of external work areas, equipment, and staging zones, supporting a safe and efficient compounding environment.
• Monitor stock levels of components, consumables, and packaging materials, ensuring timely replenishment to prevent disruption to compounding operations.

What We're Looking For:

• Ideally some experience in a cleanroom or pharmaceutical environment – full training will be given.
• Experience from another highly regulated environment such as FMCG, Food or similar manufacturing environments will be accepted.
• Knowledge of GMP and regulated production processes is a strong advantage.
• A detail‑focused approach and ability to follow strict procedures.
• Effective communication skills and a proactive, team‑oriented mindset.

Why Join?

• Excellent starting salary with bonus and structured pay increase after training.
• Full training and professional development in sterile pharmaceutical manufacturing.
• Join a respected, international business making a real impact in healthcare.
• Opportunities to build a long‑term career in a growing and secure industry.

Apply today to join a company making a difference in the healthcare sector.

Important Information:

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