Production Operative - Loughborough, United Kingdom - Digiden Ltd

Digiden Ltd

Verified Company

Loughborough, United Kingdom

1 week ago

Posted by:

Tom O´Connor

beBee Recruiter

Description

Our client Nemaura is currently seeking Production Operatives to join the Medical Device division as it embarks on the manufacturing scale-up of one of its product lines.

This is a fantastic opportunity to join a company with ambitious growth plans and become part of a growing Production Team.

The Production Operative will be required to undertake medical device manufacturing tasks, quality assurance tasks and inventory management, whist following HSE regulations.

The individual should be capable of working effectively with others from diverse backgrounds and demonstrate capability to adapt to new, different, or changing requirements.

Display strong moral principles and work ethics whilst demonstrating initiative.

The Production Operative will have an overview of the entire manufacturing process. They will be a process leader, trainer, and resident expert in a specific manufacturing process.

They are responsible for contributing to the designs and definition of production processes as well as continuous improvement of the current processes and production stage.

Reporting to the Manufacturing Manager, the Production Operative will be working within a tight knit team of other Operatives and Technicians.

The Operative is responsible for safe working practices, undertaking COSHH and risk assessments, housekeeping, investigation, and report writing.

The Operative role is suitable to someone who is adaptable, driven to complete projects, willing to problem solve and undertake root cause analysis and adaptable.

Main Responsibilities

Undertake manufacturing tasks following instructions and Standard Operating Procedures. Work safely within technical areas, maintaining excellent housekeeping and always adhering to HSE and quality management systems.
Support the validation and verification testing of product and equipment; ensuring that requirements of the Quality Management System have been met.
Report any HSE matters and identified opportunities for improvement to

- supervisors/management.

Complete required paperwork.
Operation & maintenance of production equipment and machinery.
Understand the importance of working to high standards to ensure that regulatory and compliance requirements for ISO 9001, ISO 13485 and other international regulatory requirements are achieved.

Role Requirements

Role requires lifting, carrying and moving (with aids where appropriate) inventory up to 15kg. Able to undertake tasks that require fine finger movement and experience of using hand/power tools.
Ability to work independently as well as contributing to the wider team.
Excellent communication skills both verbal and written.
Excellent time keeping and attendance.
Attention to detail.
Quality focussed.
Experience of working in a pharma/medical device/ISO 13485 regulated environment beneficial but not essential.

Job Types:
Permanent, Full-time

Schedule: