Benefits

• Monday to Friday position
• 12 month Full time contract
• Hybrid work arrangement

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

About the opportunity
The R&D Project Operations Specialist will in collaboration with subject matter experts create templates for study and regulatory documentation.

Duties

• Technical writing in collaboration with subject matter experts creates templates for study and regulatory documentation
• Generation of technical reports for use in regulatory submissions based on templates
• Preparation of regulatory CMC sections including developmental to commercial phases of a product lifecycle
• Drafting SOP, policy and working instructions documents for R&D department

Skills and Experience

• Bachelor of Science, Masters or PhD would be preferred
• Scientific background – will translate lab data into reports
• Virus Safety/pathogen safety (virology background)
• Proficiency in German language highly regarded
• Have own car and licence as travel between sites may be required
• A pharmaceutical background would be beneficial

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 12-month contract opportunity based in Melbourne with travel required occasionally to other sites.

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