Manufacturing Operator

Randstad Construction and Property; Risley; On-site; GBP 27,000 - 27,600; Full time

Benefits offered by this job

PPE provided

Full training

Job summary

Randstad CPE is seeking two Manufacturing Operators II for a 12-month contract in Warrington (7 Kingsland Grange). You will join a world-class manufacturing operation in an ISO 7 clean room, assembling cartridge products and supporting DNA reagent processes in line with SOPs.

This hands-on role requires experience in manufacturing/clean rooms, COSHH awareness, and strong manual dexterity. Overtime is available; start date ASAP. Training and PPE are provided.

Qualifications

• Proven experience in a manufacturing or clean room production environment.
• Hands-on experience with hazardous materials and COSHH guidelines awareness.
• Excellent manual dexterity and ability to handle physical tasks safely.

Responsibilities

• Assemble in a clean room, operate equipment and inspect products.
• Follow GDP and perform basic QC sampling and testing.
• Mentor and train new team members to achieve competency.
• Monitor calibration schedules for lab instruments and coordinate with maintenance.
• Coordinate with Engineering to resolve equipment issues and keep downtime low.
• Support continuous improvement via PRs and Change Orders in PLM/QA systems.

Skills

Manufacturing/clean room experience

COSHH awareness

Manual dexterity

Job description

Manufacturing Operator II

Location: Warrington (7 Kingsland Grange)

Position Type: Full-time, 12-Month Contract (Replacement Cover)

Positions Available: 2

Working Hours: 37.5 hours per week | Monday - Friday

Days: Mon-Thu 07:15-16:00 | Fri 07:15-11:45

Pay Rate: £14.01/hr (Equivalent to £27,325.00/year)

Overtime: Available

Start Date: ASAP

About the Role

We are looking for hands‑on, quality-driven Manufacturing Operators to join a world‑class manufacturing operation in Warrington.

In this role, you will work collaboratively within a dynamic team in an ISO 7 clean room environment. You will lead by example, supporting the assembly and manufacturing of specialised cartridge product lines (including gel, primary, and ladder cartridges) working with DNA reagents in accordance with strict Standard Operating Procedures (SOPs).

Key Responsibilities

• Clean room Assembly & Equipment Operation: Perform multi‑stage, semi‑automated assembly on production lines wearing full Tyvek gowning and personal hood PPE. Operate Cartridge Sealing Machines (CSM) and carry out thorough visual inspections.
• Quality & Compliance: Follow Good Documentation Practice (GDP), submit regular samples for Quality Control (QC) testing, and perform basic QC testing on intermediates and finished goods as required.
• Mentor-ship & Training: Train and support new team members, guiding them toward confident, unsupervised competency.
• Equipment & Calibration: Monitor and maintain calibration schedules for laboratory instruments to ensure timely calibration by designated equipment teams.
• Maintenance & Clean room Maintenance: Liaise with Engineering to resolve machine breakdowns promptly and minimise production downtime. Participate in regular particle reduction cleans and clean room environmental monitoring (e.g., swab preparation and taking).
• Continuous Improvement: Manage Problem Reports (PRs) and Change Orders using PLM/Quality Management software to support continuous improvement projects, update documentation, and assist with root‑cause investigations.

Requirements & Qualifications

Essential Experience & Knowledge:

• Proven experience working within a manufacturing or clean room production environment.
• Hands‑on experience with hazardous materials and solid awareness of COSHH guidelines.
• Excellent manual dexterity and ability to handle physical/manual tasks safely.

Core Skills & Attributes:

• Attention to Detail: Ability to follow written and verbal SOP instructions carefully and complete documentation to GDP standards.
• Teamwork & Independence: Strong collaborative skills alongside the ability to manage your own workload independently under the supervisor's guidance.
• Organisation & Time Management: Ability to handle tight deadlines, balance multiple priorities, and perform efficiently under pressure.
• Communication & Tech Literacy: Clear communication skills and comfortable operating standard computer terminals/office systems daily.
• Adaptability: A flexible mindset with a willingness to learn new duties, adapt at short notice, or work overtime when needed.
• Interest in Science/Engineering: A demonstrated interest or background in scientific, mechanical, or engineering processes is strongly preferred.

Working Environment & On-boarding

• PPE & On-boarding: Full training, protective equipment (PPE), and Tyvek gowning will be provided.
• Selection Process: Stage 1 on-site interview with the Hiring Manager.
• Pre-Employment Screening: Successful candidates will undergo a standard background check.

Randstad CPE values diversity and promotes equality. No terminology in this advert is intended to discriminate against any of the protected characteristics that fall under the Equality Act 2010. We encourage and welcome applications from all sections of society and are more than happy to discuss reasonable adjustments and/or additional arrangements as required to support your application.

Candidates must be eligible to live and work in the UK.