Who We Are:
Almac Group is a global leader in advancing human health. We provide a range of expert services across the drug development lifecycle to pharmaceutical and biotech companies, supporting them in finding treatments for patients.
Description:
Global Quality Document Administrator (FTC: 12 months)
Location: Craigavon
Hours: 37.5 hours per week
Salary: Competitive
Business Unit: Pharma Services
Open To: Internal & External Applicants
Ref No.: HRJOB10986
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The Role
The Global Quality Documentation Administrator plays a critical role in supporting the daily operations of the Content Suite system and ensuring the effective management of global documentation processes in alignment with Good Manufacturing Practice (GMP) and internal quality standards.
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This role is responsible for maintaining the Pharmaceutical Quality System (PQS) documentation lifecycle, managing reference and working documents, and ensuring timely execution of documentation tasks to meet departmental and business needs. The administrator also contributes to the continuous improvement of document control processes and supports global teams across APS sites through collaboration, issue resolution, and system enhancements.
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In addition to system administration, the role involves generating performance metrics, supporting investigations into documentation issues, and assisting with the expansion and migration of documents into the Content Suite system.
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The administrator is expected to be highly organised, self-motivated, and capable of maintaining high standards under pressure. They will also coordinate and participate in meetings, take minutes, and provide essential support to the Global Quality Team Leader for document management initiatives and projects. This position is vital in ensuring that documentation systems remain robust, compliant, and aligned with evolving industry expectations.
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Key Requirements
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