Responsibilities
- Formulates strategies and establishes protocols to ensure adherence to regulatory mandates.
- Exercises authority over the authorization of production, Batch Manufacturing Record (BMRs), and meticulous document review.
- Confirms the sufficiency of professional indemnity coverage for all professional activities conducted personally or under one’s purview.
- Upholds stringent compliance with Good Manufacturing Practice (GMP) standards.
- Address market grievances in collaboration with Quality Control and Quality Assurance.
- Oversees the operational activities of the regulatory unit, concentrating on compliance, license registration, and renewal.
- Maintains current awareness of evolving GMP, Pharmacovigilance, and CGMP guidelines in the realm of product development and compliance.
- Facilitates the processing and acquisition of chemical permits for Dana Group of companies.
- Assures rigorous adherence to all legal and professional prerequisites within the premises.
- Provides guidance to management and internal stakeholders to ensure meticulous regulatory compliance.
- Engages in advocacy initiatives and public corporate responsibility campaigns, fostering robust relationships with diverse business stakeholders.
Requirements
- Minimum of B.Pharm
- Minimum of 4-5 years’ experience in a pharmaceutical sales
- Excellent communication Skills
- Good negotiation and relationship management skills.
How to Apply
Interested and qualified candidates should send their CV to: vacancies@danagroup.com using the Role as the subject of the email.