R&D Document Associate
at Bell People Consultants
Melbourne VIC 3000, Victoria, Australia -
| Start Date | Expiry Date | Salary | Posted On | Experience | Skills | Telecommute | Sponsor Visa |
|---|---|---|---|---|---|---|---|
| Immediate | 24 Jun, 2024 | Not Specified | 25 Mar, 2024 | 3 year(s) or above | Communication Skills,Life Sciences,Pharmaceutical Industry | No | No |
Required Visa Status:
| Citizen | GC |
| US Citizen | Student Visa |
| H1B | CPT |
| OPT | H4 Spouse of H1B |
| GC Green Card |
Employment Type:
| Full Time | Part Time |
| Permanent | Independent - 1099 |
| Contract – W2 | C2H Independent |
| C2H W2 | Contract – Corp 2 Corp |
| Contract to Hire – Corp 2 Corp |
Description:
- Leading Pharmaceutical Global Manufacturing Organisation
- Virology Background highly desirable
- Melbourne Metropolitan Area - Long Term contract
Responsibilities:
- Create templates for study & regulatory documentation for CMC dossier, R&D reports.
- Generate technical reports for regulatory submissions & prepare regulatory CMC sections.
- Prepare regulatory CMC sections including developmental to commercial phases of products lifecycle.
- Draft SOP, policy & work instruction documents for R&D department.
- Monitor regulatory developments & advise management/key stakeholders on the potential impact of regulations on the organization
REQUIREMENT SUMMARY
Min:3.0Max:8.0 year(s)
Pharmaceuticals
Pharma / Biotech / Healthcare / Medical / R&D
Clinical Pharmacy
Graduate
Life sciences
Proficient
1
Melbourne VIC 3000, Australia
