ZS is hiring a Business Technology Solutions Associate Consultant – MLR Coordinator in Bengaluru, India. This exciting opportunity lets you manage Medical, Legal, and Regulatory (MLR) review processes, ensuring compliance and innovation in pharmaceutical promotional content. If you have expertise in life sciences and regulatory frameworks, this role could shape your career in the fast-growing healthcare consulting space.
✅ Key Responsibilities
As an MLR Coordinator at ZS, you will:
- Manage the end-to-end MLR review process for promotional and non-promotional content.
- Submit and track materials in Veeva PromoMats (or similar systems).
- Coordinate with brand teams, medical reviewers, and legal stakeholders.
- Ensure compliance with FDA, EFPIA, ABPI, and global SOPs.
- Maintain MLR dashboards, trackers, and audit logs.
- Support best practices, training, and process improvements.
- Monitor expiry timelines and manage renewals/withdrawals.
🎓 Qualifications
- Bachelor’s degree in Life Sciences, Pharmacy, Biotechnology, or related field.
- 1–3 years’ experience in MLR coordination, regulatory operations, or pharma review processes.
- Familiarity with Veeva PromoMats or similar platforms (highly desirable).
- Strong organizational and communication skills.
- Ability to multitask in a fast-paced, compliance-driven environment.
💼 Additional Skills
- Excellent verbal and written communication.
- Ability to simplify complex concepts for diverse stakeholders.
- Proficiency in virtual global team collaboration.
- Willingness to travel for client engagement and professional growth.
🌟 Perks & Benefits
ZS offers a comprehensive total rewards package, including:
- Health & wellness benefits
- Financial planning support
- Professional development & career mobility
- Flexible hybrid work model
- Global exposure and cross-functional growth opportunities
