Associate Regulatory Specialist
at Ecolab
PDA, Provincia Alajuela, Costa Rica -
Start Date | Expiry Date | Salary | Posted On | Experience | Skills | Telecommute | Sponsor Visa |
---|---|---|---|---|---|---|---|
Immediate | 19 Jan, 2025 | Not Specified | 19 Oct, 2024 | N/A | Cas,Management Skills,English,Communication Skills,Epic,Central America,Sap | 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:
Join Ecolab as an Associate Regulatory Specialist. This position is primarily responsible for Hygienic Products and Chemical registration in Central America and Caribbean. Drug Precursor Regulations assessment is required.
MINIMUM QUALIFICATIONS:
- Bachelor’s degree, preferably in a technical field
- Previous professional experience
PREFERRED QUALIFICATIONS:
- Ability to learn business and regulatory processes
- Good written and verbal communication skills (both Spanish and English)
- Ability to read and interpret technical and regulatory documents
- Good data management skills, including attention to detail
- EPIC, CAS and SAP system experience
- Familiarity with regulatory programs in Central America and US
- Knowledge of general label composition requirements for any regulated products.
- Product registration or certification experience
- Ability to drive others to get things done
- Detail oriented
- Self Starter
- Technical writing experience
Responsibilities:
- Maintain product registration renewals, including management of registration databases
- Compilation and submission of label/formula notification/amendments for registration purposes
- Frequent contact with state agencies and contractors for purposes of registration
- Becoming familiar with regulations applicable to specific areas of responsibility, which may include agency exposure
- Registration file management, both electronic and paper
- Completing assignments as directed and handle minor compliance issues while escalating issues as needed
- Support enterprise projects to support business growth and compliance
- Additional duties as assigned
REQUIREMENT SUMMARY
Min:N/AMax:5.0 year(s)
Information Technology/IT
Pharma / Biotech / Healthcare / Medical / R&D
Software Engineering
Graduate
A technical field
Proficient
1
Provincia de Alajuela, Costa Rica