How do I apply for the Production Assistant position at LGC and track my application?

We provide a direct link to the official application portal. You can apply directly here . Additionally, you can easily track this and other applications by clicking the bookmark icon to save it to your YGI Kanban board .

What are the working arrangements and expected duration for the Production Assistant role?

This position is a full-time, structured as a on-site role.

What educational background or degree level is required for the Production Assistant at LGC?

Candidates are generally expected to be holding or pursuing the following degree levels: Bachelor.

Does LGC provide visa sponsorship or assistance for international applicants?

Regarding visa assistance and sponsorship for this role, the official status is currently listed as: Not disclosed.

Production Assistant

LGC

Found 1 week ago

Location

Maine, United States

Time

Full-time

Work Mode

On-site

Salary

Not disclosed

Visa Help

Not disclosed

Last Verified

1 week ago

Education

Bachelor

Skills & Qualifications

Technical Skills

ISO 13485
GMP
ISO 9001

Soft Skills

precision
care
accuracy
organized
efficient
flexibility
proactive approach
dedication to education and personal growth
Computer literacy

Job Description

Are you ready to be part of an exceptionally ambitious team working on innovative research? As a Production Assistant at LGC, you will play a key role in ensuring the flawless execution of our production processes. Your work will support the creation of high-quality products that compete on a global scale.

Requirements

Labelling, filling, and packaging of Multichem products with precision and care.
Receipt, pooling, and filling of plasma, ensuring strict adherence to quality standards.
Responsible for the accurate storage of supplies and products, maintaining an organized inventory.
Daily cleaning of production equipment to ensure a pristine and efficient work environment.
Assist in the manufacture of serum components and chemistry bases for QC controls, contributing to our world-class quality assurance processes.
Ensure that all work is completed in a manner aligned with the requirements of ISO 13485, GMP, and the Technopath Quality Management System.
Perform other related duties as assigned, demonstrating flexibility and a proactive approach to supporting our production team.
Leaving certificate or equivalent, demonstrating your dedication to education and personal growth.
Computer literacy, essential for efficiently managing production processes and documentation.
Experience of working in an ISO 9001, ISO 13485, IMB/FDA regulated environment is desirable, showcasing your ability to successfully implement strict quality standards.

Biology and Biotech

Biology Lab & Research

Nice to Haves

Experience of working in an ISO 9001, ISO 13485, IMB/FDA regulated environment is desirable, showcasing your ability to successfully implement strict quality standards.

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21Open Positions

Open Positions

21Open Positions

Production Assistant

Education

Skills & Qualifications

Technical Skills

Soft Skills

Job Description

Requirements

Related Field

Related Subfield

Nice to Haves