IVDR (In Vitro Diagnostic Regulation) Specialist
at Revvity
Turku, Etelä-Suomi, Finland -
| Start Date | Expiry Date | Salary | Posted On | Experience | Skills | Telecommute | Sponsor Visa |
|---|---|---|---|---|---|---|---|
| Immediate | 26 Oct, 2024 | Not Specified | 27 Jul, 2024 | N/A | Communication Skills,Molecular Biology,Biochemistry,Genetics,English,Technical Documentation,Biotechnology | 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:
The Turku Site, with over 500 employees, represents one of Revvity’s major manufacturing and product development sites for newborn, maternal fetal health, and prenatal screening. As the global market leader in newborn screening, our solutions have tested over 700 million babies worldwide for life-threatening diseases.
Now we are looking for candidates for the position IVDR (In Vitro Diagnostic Regulation) Specialist. It is a fix-term contract position to the end of March 2025.
Responsibilities:
ROLE DESCRIPTION:
- You will update product technical documentation to meet IVDR requirements.
- You will collaborate with R&D, Regulatory Affairs, and Quality.
ROLE REQUIREMENTS:
- Degree in Biochemistry, Biotechnology, Molecular Biology, Genetics, or similar.
- IVDR knowledge and/or experience from compiling technical documentation for medical device registrations.
- R&D background is appreciated.
- Fluent reporting and communication skills in English and Finnish
- Proactive, resourceful, independent and a good team player in the cross-functional team.
REQUIREMENT SUMMARY
Min:N/AMax:5.0 year(s)
Pharmaceuticals
Pharma / Biotech / Healthcare / Medical / R&D
Clinical Pharmacy
Graduate
Biology
Proficient
1
Turku, Finland
