Production Operative (Cleanroom)

TN United Kingdom; East Midlands; On-site; GBP 25,000 - 35,000; Full time

Job summary

An established industry player in the MedTech sector is seeking a Production Operative to join their dynamic team in the East Midlands. This exciting role offers the chance to work with cutting-edge medical devices in a cleanroom environment, adhering to GMP standards. The ideal candidate will bring experience in cleanroom manufacturing and a solid understanding of ISO 13485 standards. This is a fantastic opportunity to contribute to innovative projects while ensuring compliance with industry regulations. If you're detail-oriented and passionate about making a difference in healthcare, this role is perfect for you.

Qualifications

• Experience in a Cleanroom manufacturing facility is essential.
• Knowledge of ISO 13485 standards is required.

Responsibilities

• Manufacture class III implantables within cleanroom facilities.
• Maintain batch records and ensure GMP operations.

Skills

Cleanroom manufacturing experience

ISO 13485 standards knowledge

GMP environment operations understanding

Attention to detail

Job description

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Production Operative (Cleanroom), East Midlands, England

Client:

Page Personnel

Location:

East Midlands, England, United Kingdom

Job Category:

Other

EU work permit required:

Yes

Job Reference:

67cb53be4a4d

Job Views:

3

Posted:

05.05.2025

Expiry Date:

19.06.2025

Job Description:

• A fantastic opportunity to join a growing MedTech company developing novel class III implantables.

About Our Client

The client is a lean med-tech organization conducting clinical trials and seeking a dynamic Production Operative to strengthen their team.

Job Responsibilities

• Manufacture class III implantables within controlled cleanroom facilities following GMP standards.
• Support the Head of Operations with additional manufacturing and production activities.
• Maintain batch records, device history records, and associated documentation.
• Ensure efficient GMP operations and process optimization projects.
• Coordinate shipping of samples to third-party test houses, suppliers, and CROs as needed.

The Successful Candidate

Ideal candidates will have:

• Experience working in a Cleanroom manufacturing facility.
• Experience with ISO 13485 standards.
• Good understanding of GMP environment operations.
• Excellent attention to detail.

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

What's on Offer

An excellent opportunity to join a growing medtech company developing cutting-edge medical devices.