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Pharmabharat brings an excellent opportunity for life sciences and pharmacy professionals to join a global regulatory affairs function as an Associate โ Regulatory Affairs (RMQ) in Bengaluru. This role focuses on raw material regulatory data management, supplier coordination, and compliance across Cosmetics, OTC, Pharmaceuticals, and Food/Nutritional products.
This position is ideal for freshers and early-career professionals (0โ3 years) seeking hands-on exposure to global regulatory systems, toxicology collaboration, and end-to-end request governance.
๐งช Key Responsibilities โ Regulatory Affairs (RMQ)
๐น Raw Material Data Governance
- Initiate regulatory data requests within 24 hours of receipt.
- Ensure strict adherence to defined turnaround times (TATs).
- Understand request objectives and seek clarifications when required.
- Manage supplier communication, follow-ups, and escalation of delays.
- Maintain and update the Global Request Tracker (GTR) as the single source of truth.
- Communicate proactively with global stakeholders throughout the request lifecycle.
๐น Regulatory & Technical Expertise
- Apply regulatory knowledge for raw materials across:
- Cosmetics
- OTC products
- Pharmaceutical drugs
- Food & Nutritional products
- Review toxicology and safety-related documentation.
- Collaborate closely with Toxicology teams to gather accurate supplier data.
- Ensure right-first-time data collection with high accuracy and completeness.
- Maintain end-to-end data connectivity across regulatory systems.
๐น Ownership & Quality Focus
- Deliver all requests on time and error-free.
- Meet or exceed defined KPIs for quality and productivity.
- Demonstrate strong ownership and accountability.
๐ฏ Required Skills & Competencies
โ Must-Have Soft Skills
- Project & Request Management: Ability to handle high-volume regulatory requests efficiently.
- Attention to Detail: Disciplined execution with flawless documentation.
- Communication Skills: Clear, timely, and professional interaction with internal teams and suppliers.
- Problem Solving & Critical Thinking: Practical, time-bound decision-making.
- Sense of Urgency & Learning Agility: Quick adaptation in fast-paced environments.
- Resilience & Agility: Capability to perform under tight deadlines.
๐ Qualifications & Eligibility
- Education:
B.Pharm / M.Pharm / M.Sc (Life Sciences, Chemistry, Toxicology, or related disciplines) - Experience:
0โ3 years in Regulatory Affairs, Raw Material Compliance, Quality, or Data Management
(Freshers with strong regulatory knowledge may apply)
๐ผ Salary & Benefits
- Expected Salary: โน4,00,000 โ โน7,00,000 per annum (INR)
- Exposure to global regulatory frameworks
- Work with cross-functional toxicology and regulatory experts
- Strong learning and career growth opportunities
- Structured processes and performance-driven environment
๐จ How to Apply
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