Senior R&D Qa Associate, Procedural Document Specialist - 28539

Benefits Join a market leading global pharmaceutical dedicated to innovation and personal developmentOpporunity to collaborate on global projects with quality assuranceFlexible working schedule with work from home availability each weekAbout the Company
Become part of a large, global Biotechnology company renowned for its expanding and positive culture.

About the Opportunity
As the Senior R&D QA Associate, Procedural Document Specialist, you will assist the Global R&D QA department in managing Document Management Systems (DMS) to support the R&D Quality Management System.

Duties Oversee the content and upkeep of the DMS system for R&D QualityCoordinate document management workflow activities for team membersSupport global R&D and QA teams in GXP compliance, ensuring procedural document management adheres to GXPs, legal, and regulatory standardsConduct extensive database tasks, including receiving, reviewing, and formatting Word documentsRoute documents for approval, handle their return, and assign effective datesPerform necessary database clean-upSkills and Experience Degree in business, communication, technology, or a science-related fieldProficient in Microsoft Word, especially in formattingStrong attention to detailExperience with databasesExperience working in a regulated environment (R&D or manufacturing)Culture
Though a large, global company, it maintains a family-like culture and is dedicated to improving lives.

Why This Opportunity is Right for You
This is a full-time, 6-month contract position based in Melbourne. The role is hybrid, requiring 2 days in the office, Monday to Friday.

How to Apply
Click apply or contact Rohan Lallbeeharry, Senior Consultant, at 03 9938 7115for a confidential discussion.





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