Executive Regulatory Affairs Job in Septodont Healthcare India Pvt. Ltd
Executive Regulatory Affairs
- Navi Mumbai, Thane, Maharashtra
- Not Disclosed
- Full-time
- Permanent
The position will be an Executive level in RA department. Main focus of the candidate will be handling Pharmacovigilance & Regulatory compliance activity.
Profile and job description
Scope & Missions:
Complaints management quality & safety
Product complaint management ( to be confirmed with QA)
Centralization of PC
Supervise investigation and conclusion
Communication of the result to customer and others stakeholders involved inthe process
Reporting & metrics
Maintenance Quality System management for product complaint management
Vigilance:
Local QPPV in India
Implementation of the process according to Corporate SOP
Unique contact point for safety notification in Indian territories
Initiate case processing ( send to corporate)
Documentation of case
Local literature in key local publication in order to identify some case report published in the literature
Local regulatory watch
Local PSUR schedule management and PSUR management for local products ( if any)
Local signal detection for local products if any
Management of dealers and distributors: SDEA, audit, reconciliation .
Maintenance of Quality system management
Maintenance of PVMF according to template provided by Corporate
Regulatory Compliance activity:
Ensuring compliance with regulations set by the CDSCO Indian FDA, Medicines andHealthcare products Regulatory Agency (MHRA), USFDA, EU guidelines and other regulatory bodies
Creating and/or maintaining technical files and other regulatory documents / files related to products license, new product registrations or site specific manufacturing registration / re-registration
Uploading the documents in SUGAM portal and verifying updates or status
Liaising with certification / notifying body for system and product certification
Medical information management
Administrative tasks for regulatory submission
KEYExpertise :
Strong knowledge in pharmacovigilance, Regulatory compliance & Product Complaint management ( EU regulation, GVP,)
Case processing
PSUR
Quality system management
Medical device vigilance knowledge would be interesting
Pharmacist having 3 or 4 years experience
Skills :
Rigorous, organized.
Ability to deal with different type of activities
Location: Taloja, Navi Mumbai
3 to 4 Years
2 - 4 Hires