Regulatory Affairs Coordinator (Contractor)

About the role

We are looking for a Regulatory Affairs Coordinator to support product registration and lifecycle management for Abbott’s Established Pharmaceuticals Division. The role involves ensuring compliance with local regulatory requirements and collaborating with cross‑functional teams to bring branded generic medicines to market.

Key responsibilities

• Prepare and submit regulatory dossiers for new product registrations, renewals and variations.
• Develop and implement regulatory plans aligned with business objectives.
• Coordinate with global and local regulatory teams throughout the product lifecycle.
• Work closely with manufacturing, quality, development, marketing, medical and logistics teams to ensure timely and compliant execution.
• Review and approve promotional materials according to regulatory guidelines.
• Liaise with local regulatory authorities and maintain external relationships.
• Ensure adherence to regulatory and quality SOPs and identify process improvement opportunities.
• Manage documentation, archiving and submission tracking.
• Support submissions for promotional activities, symposiums and congresses.
• Contribute to training initiatives and promote a culture of compliance.

Required profile

• Bachelor’s degree in Pharmacy (Pharmacist qualification preferred).
• Experience in regulatory affairs within the pharmaceutical industry.
• Strong understanding of regulatory registration processes, product lifecycle management and compliance requirements.
• Excellent communication and stakeholder management skills.

Required skills

What we offer

• Career development opportunities within a global healthcare leader.
• Access to international training and growth programs.
• Inclusive workplace recognized for diversity and work‑life balance.