Production Operative (Cleanroom)

Michael Page (UK); Leicester; On-site; GBP 25,000 - 35,000; Full time

Job summary

Join a forward-thinking MedTech company dedicated to developing innovative implantable devices. As a Production Operative, you'll play a key role in manufacturing Class III implantables within a controlled cleanroom environment, adhering to GMP guidelines. This position offers the chance to contribute to cutting-edge medical technology while ensuring quality and compliance. If you have a keen eye for detail and a passion for improving manufacturing processes, this is the perfect opportunity for you to advance your career in a dynamic and growing organization.

Qualifications

• Experience in a Cleanroom manufacturing environment is essential.
• Hands-on experience with ISO 13485 standards is required.

Responsibilities

• Manufacture Class III implantables in cleanroom facilities.
• Support operations and maintain batch records.

Skills

Cleanroom manufacturing experience

ISO 13485 standards

GMP operations understanding

Attention to detail

Job description

Job Opportunity: Production Operative in MedTech

A fantastic opportunity to join a growing MedTech organization developing novel class III implantables. Currently undergoing clinical trials, they are seeking a dynamic Production Operative to bolster their team.

About Our Client

The client is a lean MedTech organization focused on developing innovative implantable devices. They are actively engaged in clinical trials and are looking for a proactive Production Operative to join their team.

Job Description

As a Production Operative, you will:

1. Manufacture Class III implantables within controlled cleanroom facilities following GMP guidelines.
2. Support the Head of Operations with additional manufacturing and production activities as required.
3. Produce and maintain batch records, device history records, and associated documentation.
4. Support efficient GMP operations and lead manufacturing activities, including process optimization projects.
5. Coordinate shipping of samples to third-party test houses, suppliers, and CROs as necessary.

The Successful Applicant

To be successful, you will have:

• Experience working within a Cleanroom manufacturing environment.
• Hands-on experience operating under ISO 13485 standards.
• A good understanding of GMP environment operations.
• Excellent attention to detail.

The role is fully site-based in Nottingham, Monday to Friday.

What's on Offer

This is a fantastic opportunity to join a growing MedTech company developing cutting-edge medical devices.