Benefits

• Be part of a supportive and stable working environment
• Working within a global team
• Monday to Friday role

About the company
Work within a large global Biotechnology company that boasts a good company culture that is always expanding.

About the opportunity
The Senior R&D QA Associate, Procedural Document Specialist will work as part of the Global R&D QA department assisting the R&D QA Quality Systems organisation with management of the Document Management Systems (DMS) activities to support the R&D Quality Management System.

Duties

• The Senior R&D QA Associate will be responsible for the overall content and maintenance of the DMS system on behalf R&D Quality and will coordinate document management workflow activities for personnel 
• Provides support for global R&D and QA organisation in GXP compliance related matters, including assurance that all aspects of procedural document management comply with GXPs, legal, regulatory requirements
• Extensive database work receiving documents for routing, review documents, formatting of Word documents
• Routing documents for approval
• Receiving documents back and adding effective date
• Database clean up as required

Skills and Experience

• Must have degree in relevant business, communication, technology or science discipline
• Excellent Microsoft Word skills, particularly in formatting
• Strong Attention to Detail
• Database experience
• Working in a regulated environment (R&D or manufacturing)

Culture
Although a large, global company, they are able to provide a family-like culture and prides itself in improving the lives of others.

Why this opportunity is right for you
This is a Full-time 7-month contract opportunity based in Melbourne. This is a hybrid position with 2 days required working in the office Monday to Friday only.

How to Apply
Click apply or contact Jo Turner, Senior Specialist Manager on 03 9938 7120 for a confidential discussion.