Madras Pharmaceuticals, a reputed Contract Research and Manufacturing Services (CRAMS) company, is inviting applications for the position of Regulatory Affairs Executive / Jr. Executive in T. Nagar, Chennai. This opportunity is ideal for B.Pharm or M.Pharm professionals with 4–7 years of experience in regulatory affairs, especially those experienced in preparing regulatory dossiers for emerging markets.
The role involves managing regulatory submissions, health authority queries, and product registration requirements. Candidates with strong knowledge of global regulatory guidelines and dossier preparation can build a rewarding career in the regulatory affairs domain with this pharmaceutical organization.
This Regulatory Affairs Executive job in Chennai is a great opportunity for professionals seeking growth in pharma regulatory affairs, dossier preparation, and compliance management within a CRAMS environment.
Job Details
- Company: Madras Pharmaceuticals
- Department: Regulatory Affairs
- Position: Jr. Executive / Executive – Regulatory Affairs
- Location: T. Nagar, Chennai, Tamil Nadu, India
- Qualification: B.Pharm / M.Pharm
- Experience: 4–7 Years in Regulatory Affairs
- Industry: Pharmaceutical / CRAMS
Key Responsibilities
Candidates selected for the Regulatory Affairs Executive position at Madras Pharmaceuticals will be responsible for:
- Preparing and compiling regulatory dossiers for emerging markets.
- Managing health authority queries and ensuring timely responses.
- Ensuring regulatory compliance as per global regulatory guidelines.
- Reviewing regulatory submissions and preparing responses to regulatory authority queries.
- Coordinating licensing requirements and sample submissions for product registration.
- Supporting regulatory strategy and documentation for pharmaceutical products.
- Maintaining accurate regulatory records and documentation.
Required Qualifications
To apply for this Regulatory Affairs Executive job in Chennai, candidates should meet the following criteria:
- Education: B.Pharm or M.Pharm from a recognized university.
- Experience: 4–7 years of experience in pharmaceutical regulatory affairs.
- Strong experience in regulatory dossier preparation for emerging markets.
- Knowledge of regulatory guidelines, product registration processes, and compliance standards.
- Ability to handle health authority queries and regulatory documentation efficiently.
Preferred Skills
- Experience working with pharmaceutical regulatory submissions.
- Strong documentation and regulatory writing skills.
- Familiarity with global regulatory frameworks and emerging market regulations.
- Excellent coordination and communication abilities.
Salary & Benefits
- Estimated Salary Range: ₹6,00,000 – ₹10,00,000 per year (based on experience and expertise).
- Opportunity to work with a leading pharmaceutical CRAMS organization.
- Exposure to global regulatory affairs processes and emerging market submissions.
- Professional growth in pharmaceutical regulatory compliance and dossier management.
How to Apply
Interested and eligible candidates with relevant regulatory affairs experience in the pharmaceutical industry can apply by sending their updated resume to:
📧 Email: recruiter@madraspharma.com