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Senior R&D QA Associate, Procedural Document Specialist

Job description

Benefits
  • 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.