Regulatory Life Cycle Manager- Non Medicinal
at Bayer
Reading, England, United Kingdom -
| Start Date | Expiry Date | Salary | Posted On | Experience | Skills | Telecommute | Sponsor Visa |
|---|---|---|---|---|---|---|---|
| Immediate | 01 Feb, 2025 | Not Specified | 02 Nov, 2024 | N/A | Good communication skills | 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:
Responsibilities:
- Prepare and maintain medical devices technical files and lead post-market activities such as variations, renewals, and annual reports.
- Develop and implement regulatory strategies for the life cycle management of medical devices, Drug-Device Combination products, and digital health products.
- Proactively communicate regulatory strategies, risks, and key issues throughout the life cycle to project teams and other stakeholders.
- Ensure compliance with global regulatory requirements, and other relevant regulations.
- Collaborate with Product Innovation and Regulatory Intelligence Clusters, stay abreast of changes in regulations and standards, and communicate potential impact to the organization.
- Provide support for internal and external audits.
REQUIREMENT SUMMARY
Min:N/AMax:5.0 year(s)
Pharmaceuticals
Pharma / Biotech / Healthcare / Medical / R&D
Clinical Pharmacy
Graduate
Proficient
1
Reading, United Kingdom
