Regulatory Affairs (DRAP – Medical Devices) Full Time

About Us:

Global Clinical Cura Pvt Ltd is a leading supplier of state-of-the-art medical equipment and pharmaceutical products. Committed to enhancing healthcare quality, we provide innovative solutions that cater to the diverse needs of medical professionals and institutions nationwide. Our extensive product range, from advanced diagnostic tools to essential pharmaceutical supplies, ensures that healthcare providers have access to the best resources to deliver superior patient care. At Global Clinical Cura Pvt Ltd, we combine cutting-edge technology with unparalleled service to support the ever-evolving demands of the medical industry.

We are currently seeking for a Regulatory Affairs Officer who manage and ensures the appropriate licensing, marketing and legal compliance of medical devices. The role function is a link between company and regulatory authority, ensuring that products are marketed and distributed in compliance with appropriate legislation. He / She guarantees shared understanding and alignment on all dossiers or projects.

Key Responsibilities:

1. Visits and Document Submission:

Visit and Follow-up for the for the submission of notification/registration/authorization dossiers.

2. Portfolio Distribution:

Ensure that the portfolio of products is distributed in compliance with the approved authorization, regulatory guidelines and legislation.

3. Relationship Building:

Develop and nurture strong relationships with government officials, regulatory agencies, and local authorities.

4. Legislative Monitoring:

Monitor legislative changes, policies, and regulations impacting the medical industry.

5. Coordination with Legal and Compliance:

Coordinate with legal and compliance teams to ensure adherence to all regulatory requirements.

6. Approvals and Licensing:

Obtain necessary approvals, permits, and licenses for medical devices.

7. Internal Stakeholder Communication:

Provide timely updates to internal stakeholders on changes in regulatory landscapes.

8. Reporting and Briefings:

Prepare reports and briefings on government-related matters for senior management.

9. Issue Resolution:

Address and resolve government-related issues that may impact company operations.

10. Collaboration for Compliance:

Collaborate with internal departments to ensure compliance with local departments.

Qualifications:

Bachelor’s or Master’s degree in a relevant field from a recognized institution.

Must have 2-3 years’ experience in Registration of Medical Devices.

Location: Candidates near DHA and Bahria are encouraged to apply.

Job Types: Full-time, Contract
Contract length: 24 months

Pay: Rs75,000.00 – Rs100,000.00 per month

Application Question(s):

• What is your location (Area)?
• How early can you join?
• What is your expected salary?

Experience:

• Regulatory Affairs: 1 year (Required)