Industry: Medical Devices
About the Role
We are seeking a detail-oriented Regulatory Compliance Officer responsible for ensuring full compliance with the requirements of the Drug Regulatory Authority of Pakistan (DRAP).
The ideal candidate will maintain an in-depth and continuously updated understanding of DRAP regulations, ensure internal systems align with regulatory standards, and prepare the organization for successful external audits.
This role is critical in maintaining licensing integrity, operational compliance, and audit readiness across all relevant functions.
Key Responsibilities
- Maintain up-to-date knowledge of all DRAP regulations, guidelines, and compliance updates
- Ensure organizational processes, documentation, and operations meet regulatory requirements
- Conduct regular internal compliance audits to identify gaps and non-conformities
- Develop and implement corrective and preventive actions (CAPA) for audit findings
- Prepare all documentation and systems for external regulatory inspections and audits
- Liaise with internal departments to ensure adherence to SOPs and regulatory frameworks
- Maintain complete and audit-ready compliance documentation and records
- Monitor regulatory changes and communicate updates to relevant stakeholders
- Support quality assurance functions in maintaining compliance standards
Required Skills & Knowledge
- Strong understanding of DRAP regulatory framework and pharmaceutical compliance systems
- Knowledge of Good Manufacturing Practices (GMP) and audit procedures
- Experience in internal audits, compliance checks, or regulatory inspections
- Strong documentation, reporting, and analytical skills
- Ability to interpret regulatory guidelines and translate them into operational requirements
- High attention to detail and structured thinking
- Experience in pharmaceutical or medical device industries
Preferred Experience
- 1–5 years in regulatory affairs, quality assurance, or compliance roles
Work Environment
- Professional, compliance-driven organizational setting
- Cross-functional coordination with QA, production, and management teams
Why Join Us
- Direct involvement in regulatory compliance and audit readiness
- Exposure to DRAP inspection processes and industry best practices
- Opportunity to strengthen expertise in pharmaceutical regulatory systems
Pay: Rs70,000.00 - Rs90,000.00 per month
Work Location: In person