Exciting Opportunity: Join as an Associate – Regulatory Affairs (RMQ) in Bengaluru!

Are you a recent graduate looking to launch your career in Regulatory Affairs? Do you have a passion for ensuring compliance and quality in the pharmaceutical industry? If yes, this is the perfect opportunity for you! 📍

About the Role 📝

As an Associate – Regulatory Affairs (RMQ), you will play a crucial role in managing raw material data and ensuring compliance with regulatory requirements. Your responsibilities will include:

End-to-end request governance for raw material data management

Technical expertise in regulatory requirements for raw materials

Maintaining data accuracy and integrity

Collaborating with global stakeholders and suppliers

Providing timely and effective communication

Sustaining an ownership mindset and meeting KPIs

Requirements 📚

0-3 years of experience (freshers welcome)

Strong knowledge of regulatory requirements and toxicology

Excellent communication and project management skills

Ability to work in a fast-paced environment

Attention to detail and analytical skills

What We Offer 🌈

Opportunity to work in a dynamic and innovative environment

Competitive salary and benefits package

Professional growth and development opportunities

Collaborative and supportive team culture

How to Apply 📧

If you’re interested in this role, apply now 👇🏻:

https://job-boards.eu.greenhouse.io/clinchoice/jobs/4691058101?source=LI

Interview Book

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About the Company 🌐

The company is a leading player in the pharmaceutical industry, committed to delivering high-quality products and services.

Conclusion 🌟

Don’t miss this amazing opportunity to kick-start your career in Regulatory Affairs! Apply now and take your career to the next level! 🌟

Here’s a detailed explanation of the role and responsibilities:

End-to-End Request Governance 📝

As an Associate – Regulatory Affairs (RMQ), you will be responsible for managing raw material data requests from initiation to completion. This includes:

Initiating requests within 24 hours of receipt

Adhering to standard turnaround times (TAT)

Understanding the objective of the request and seeking clarification if needed

Handling supplier communication effectively

Updating and maintaining the Global Request Tracker (GTR)

Technical Expertise 📚

You will be expected to have a strong understanding of regulatory requirements for raw materials, including:

Knowledge of toxicology and safety assessment

Maintaining data accuracy and integrity

Collaborating with toxicology partners

Ensuring data connectivity across systems

Soft Skills 🤝

The ideal candidate will have:

Excellent project management skills

Disciplined execution and attention to detail

Effective communication skills

Problem-solving and critical thinking abilities

Sense of urgency and learning agility

Agility and resilience in a fast-paced environment

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