Join a market leading global pharmaceutical dedicated to innovation and personal development
Opporunity to collaborate on global projects with quality assurance
Flexible working schedule with work from home availability each week
About 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 Quality
Coordinate document management workflow activities for team members
Support global R&D and QA teams in GXP compliance, ensuring procedural document management adheres to GXPs, legal, and regulatory standards
Conduct extensive database tasks, including receiving, reviewing, and formatting Word documents
Route documents for approval, handle their return, and assign effective dates
Perform necessary database clean-up
Skills and Experience
Degree in business, communication, technology, or a science-related field
Proficient in Microsoft Word, especially in formatting
Strong attention to detail
Experience with databases
Experience 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 7115 for a confidential discussion.