Medreich Hiring Regulatory Affairs Executive (UK/EU & AU/NZ Markets)

Medreich, a prominent player in the global pharmaceutical industry and part of the Meiji Group, is currently looking for Regulatory Affairs Executives to join their team in Bangalore. The ideal candidates should possess 3-6 years of experience in core regulatory affairs with a formulation background. This opportunity covers both UK/EU and AU/NZ markets, offering candidates a challenging and rewarding environment to contribute to international regulatory strategies.

If you’re looking for a role where you can apply your regulatory expertise and work on global projects, this could be the perfect opportunity for you.

Job Responsibilities

As a Regulatory Affairs Executive at Medreich, you will be responsible for handling regulatory submissions and approvals for the UK/EU and AU/NZ markets. The role demands a strong understanding of global regulatory frameworks and a formulation background to ensure smooth compliance with local and international regulations.

Key Responsibilities Include:

• Managing pre-approval and post-approval submissions for the UK/EU and AU/NZ markets.
• Developing and preparing regulatory strategies to comply with the requirements of health authorities.
• Handling product registrations, license renewals, and other regulatory submissions.
• Coordinating with cross-functional teams including R&D and Quality Assurance to gather required documentation for regulatory submissions.
• Staying updated on regulatory changes and ensuring compliance with local and international standards.
• Communicating with regulatory agencies for timely approvals.

Qualifications

To be eligible for the Regulatory Affairs Executive position, candidates must have a robust background in regulatory affairs and possess the following qualifications:

Must-Have:

• A Bachelor’s or Master’s Degree in Pharmacy (B.Pharm/M.Pharm) or M.Sc. in related fields.
• 3-6 years of experience in Regulatory Affairs within the pharmaceutical industry, specifically with a formulation background.
• Pre-approval experience for the UK/EU market with 4-6 years of hands-on experience.
• Post-approval experience for UK/EU markets with 3-5 years of regulatory work.
• AU/NZ regulatory experience with 4-6 years of experience is required for the AU/NZ team position.

Preferred:

• Candidates with strong knowledge of global regulatory requirements and submission processes.
• Professionals who are available to join the team immediately.

Note: Freshers are not eligible to apply for this position.

Location

The position is based in Bangalore

How to Apply

If you meet the qualifications and are eager to work in a globally respected company, send your CV to sekhar.s@medreich.com. Medreich is looking for driven professionals who are ready to make an impact in the regulatory affairs domain. Do not apply if you are a fresher, as this position requires significant industry experience.