Administrator (Quality Assurance)

Posted 8 Days Ago
Be an Early Applicant
Tipperary
Entry level
Food • Healthtech • Biotech
The Role
As a Quality Assurance Administrator, you will oversee the management of Quality documentation, process document change requests, ensure accurate record-keeping, support the Internal Audit program, and help enforce compliance with quality standards.
Summary Generated by Built In

Company Description

Join Technopath as a Quality Assurance Administrator 

Are you ready to play a pivotal role in maintaining and enhancing our quality management systems?

At Technopath, we're dedicated to ensuring the highest standards in our products and processes, and we're seeking a talented individual to join our team as a Quality Assurance Administrator to support with maintaining raw material specifications, reviewing certificates of analysis, and performing visual inspections.

Job Description

As a Quality Assurance Administrator you will be responsible for coordinating the control, distribution, and management of Quality documentation that supports our quality management systems. This includes processing and approving document change requests and ensuring timely notification of changes to relevant parties. Additionally, you'll be tasked with maintaining various logs for tracking documentation and tasks, ensuring accuracy and efficiency in our processes.

Supporting our Internal Audit program will be another key aspect of your role, where you'll participate in audits and implement corrective actions, as necessary. It's important that you demonstrate or have a desire in understanding Quality Policies and system procedures, and the process to promptly report any noncompliance issues to management.

Qualifications

To thrive in this administrative role within Quality Assurance, you’ll need a sharp eye for detail and an impressive ability to manage complex documentation with precision.

Success here hinges on a solid administrative background, as you'll be at the heart of coordinating, distributing, and managing quality documentation. Experience with FDA 21CFR820, ISO13485, IVDD98/79/EC, and IVDR EU/2017/746 is desirable, but rest assured—comprehensive training will be provided.

If you enjoy working in a collaborative environment, we’d love to have you join our dynamic team!

Additional Information

LGC, Diagnostics & Genomics (D&G) is committed to creating a diverse and inclusive workplace where everyone is valued and respected. We believe in equal opportunity for all employees and applicants, regardless of race, color, religion, gender, sexual orientation, national origin, age, disability, or any other legally protected status.

We actively seek to foster an environment where all individuals can thrive and contribute to our shared success. Our hiring practices are designed to ensure that all candidates are treated fairly and evaluated based on their qualifications, merit, and alignment with our organizational values.


#IJLGC

The Company
Teddington
1,459 Employees
On-site Workplace

What We Do

LGC is a leading, global life science tools company, providing mission-critical components and solutions into high-growth application areas across the human healthcare and applied market segments. Its high quality product portfolio is comprised of mission-critical tools for genomic analysis and for quality assurance applications, which are typically embedded and recurring within our customers’ products and workflows and are valued for their performance, quality and range.

LGC’s tools play a key role in customer workflows from discovery applications through to commercial manufacture and enable its customers to: bring new diagnostics and therapies to market; progress research and development; optimise food production; and continuously monitor and enhance the quality of food, the environment and consumer products.

LGC’s 175+ years of scientific heritage, combined with a track record of innovation and value-enhancing acquisitions, has enabled the company to build its product portfolio and expertise, and develop deep relationships with customers, industry partners and the global scientific community.

LGC’s core purpose of Science for a safer world and its core values of passion, curiosity, integrity, brilliance and respect, drive its culture. As of 30 June 2021, it employs 4,350 employees, of which over 1,175 employees hold PhD and/or master’s degrees. Its products and services are delivered by highly qualified and experienced teams, operating from a global network of accredited sites that showcase its scientific and manufacturing capabilities.

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