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Form of work
Salary- Monday to Friday position
- 12 month Full time contract
- Hybrid work arrangement
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
- 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
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 7*** for a confidential discussion.
