Abbott Regulatory Affairs Specialist (1 year contract) in Singapore, Singapore
- To compile Dossiers for ADD IVD products for submission to relevant government authorities, and other Regulatory/Quality and Compliance related issues.
To compile Technical Dossiers for ADD IVD products for submission into government authorities
To answer queries from local authority on submitted Dossiers
To liaise with Global Regulatory Affairs team on technical files availability
Assist RA&QA Manager on other QA matters such as Field Recall or Corrective Action
Ensure pre-market and post market activities are carried out with due diligence and on time.
Bachelor's degree in Biomedical Science, Bioengineering/Pharmacy
Fresh graduates are welcomed to apply for this position
1-2 years working experience in a similar industry and/or hospital laboratory/diagnostics/regulatory capacity preferred
Strong analytical skills and troubleshooting abilities
Good communication skills
An Equal Opportunity Employer
Abbot welcomes and encourages diversity in our workforce.
We provide reasonable accommodation to qualified individuals with disabilities.
To request accommodation, please call 224-667-4913 or email firstname.lastname@example.org