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Quality Document Administrator

TN United Kingdom

Craigavon

On-site

GBP 25,000 - 35,000

Full time

6 days ago

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An established industry player is seeking a Quality Document Administrator to join their Document Control team. In this pivotal role, you will manage the compilation, issuance, and review of GMP documentation, ensuring compliance with quality standards. Your expertise will contribute to the efficient functioning of the Quality system, while you collaborate across departments to maintain essential documentation. This position offers a dynamic working pattern, allowing you to thrive in a flexible environment. If you are passionate about quality assurance and eager to support continuous improvement initiatives, this opportunity is perfect for you.

Eligibility to work in the UK or valid work permit required.
Experience in quality systems or manufacturing environments preferred.

Manage GMP documentation essential for the company's Quality system.
Collaborate with departments to retrieve and distribute GMP documentation.

Quality System Management

Documentation Control

Collaboration

Data Analysis

A-Level (or equivalent)

Quality Document Administrator, Craigavon

Client:

Almac Group

Location:

Job Category:

Other

EU work permit required:

Yes

Job Reference:

1736ca193c44

Job Views:

Posted:

18.04.2025

Expiry Date:

02.06.2025

Job Description:

Quality Document Administrator

Hours: 37.5 hours per week

Business Unit: Pharma Services

Open To: Internal & External Applicants

Ref No.: HRJOB10487

The Role

As a part of the Document Control team at Almac Pharma Services, the role involves managing the compilation, issuance, and review of GMP documentation essential for maintaining the company's Quality system.

The post holder will be responsible for generating various GMP documents, such as Manufacturing and Packaging Specifications, SOPs, and validation documentation in approved formats. They will also play a key role in issuing batch records, circulating quality system-related documentation, managing controlled documents, and ensuring the organization of Document Control storage areas.

Additionally, the post holder will collaborate with different departments to retrieve and distribute GMP documentation, maintain quality system indexes, and participate in data collation for QA reports and investigations, contributing to the efficient functioning of the Quality system.

Furthermore, the position entails participating in investigations, trending quality performance indicators, and tracking GMP-associated documentation to support continuous improvement initiatives.

Key Requirements

Have eligibility to work in the UK OR possess a valid work permit that will allow you to take up full time employment in the UK
3 x A-Level (or equivalent) at Grade C or above
Previous experience within a quality system or manufacturing environment

Further Information

The working pattern for this role is a flex pattern between the hours of 07:00 – 19:00 with core hours of 10:00 – 16:00.

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Apply online and tailor your CV to outline how you meet the role criteria. Please upload your CV in PDF format where possible.

Closing Date

We will no longer be accepting applications after 5pm on 21 April 2025

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Quality Document Administrator

TN United Kingdom

Craigavon

On-site

GBP 25,000 - 35,000

Full time

Job summary

Qualifications

Responsibilities

Skills

Education

Job description