Documentation Compliance Specialist
at Cubane Solutions AB
Stockholm, Stockholms län, Sweden -
| Start Date | Expiry Date | Salary | Posted On | Experience | Skills | Telecommute | Sponsor Visa |
|---|---|---|---|---|---|---|---|
| Immediate | 17 Jul, 2024 | Not Specified | 18 Apr, 2024 | N/A | Swedish,English,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:
ASSIGNMENT DESCRIPTION
- Quality control of all documentation to ensure compliance with rules and regulations.
- Make sure that the turnover package is according to the GMP/GDocP.
- Expedite factories and other stakeholders to supply documentation.
- Collaborate with Design/Automation/Electrical engineers, Project managers and Product supply team on daily basis.
- Cooperate with customers (as well) regarding to the turnover package requirements and deliverables.
REQUIREMENTS
- Detail-oriented, perseverant, strong communication skills, and adept at collaborating within a team environment.
- Experience in documentation management within the pharmaceutical or biotechnology sectors is highly desirable, given the diverse range of pharmaceutical clientele.
- Language: Proficiency in English is essential, and knowledge of Swedish is advantageous.
Responsibilities:
Please refer the Job description for details
REQUIREMENT SUMMARY
Min:N/AMax:5.0 year(s)
Electrical/Electronic Manufacturing
Engineering Design / R&D
Other
Graduate
Proficient
1
Stockholm, Sweden
