Tanishq Life Care, a leading pharmaceutical company known for its innovative and quality-driven healthcare solutions, has announced an exciting opportunity for an International Regulatory Affairs Executive at its Ahmedabad, Gujarat facility. Candidates with experience in pharmaceutical regulatory affairs, dossier preparation, and international product registrations are encouraged to apply.
This regulatory affairs job in Ahmedabad offers professionals the opportunity to work with global pharmaceutical markets, manage international regulatory submissions, and contribute to compliance strategies for a rapidly growing pharmaceutical organization.
About Tanishq Life Care
Tanishq Life Care is an India-based pharmaceutical company with more than two decades of experience in developing and manufacturing high-quality healthcare products. The company specializes in antibiotics, antifungals, anti-ulcer medications, multivitamins, anti-allergic and anti-inflammatory drugs, analgesics, psychiatric medicines, cardiac medications, topical formulations, and personal care products.
The organization is committed to delivering affordable, innovative, and globally compliant pharmaceutical solutions.
Job Details
| Particulars | Details |
|---|---|
| Position | International Regulatory Affairs Executive |
| Location | Ahmedabad, Gujarat, India |
| Employment Type | Full-Time |
| Workplace Type | On-Site |
| Department | Regulatory Affairs |
| Industry | Pharmaceutical Manufacturing |
Key Responsibilities
As an International Regulatory Affairs Executive, the selected candidate will:
- Prepare, review, and submit regulatory dossiers for international markets.
- Compile CTD and eCTD dossiers according to country-specific requirements.
- Coordinate with Formulation Development, Quality Assurance, Quality Control, and Production departments.
- Monitor international regulatory guidelines and updates.
- Support global product registration activities.
- Respond to regulatory authority queries and deficiency letters.
- Maintain regulatory databases and submission records.
- Ensure ongoing compliance with international pharmaceutical regulations.
- Assist during regulatory audits and inspections.
- Support lifecycle management activities for approved products.
Required Qualifications
Candidates applying for this pharmaceutical regulatory affairs job should possess:
Educational Qualifications
- Bachelor’s Degree in Pharmacy (B.Pharm)
- Master’s Degree in Pharmacy (M.Pharm)
- Life Sciences
- Chemistry
- Related scientific disciplines
Experience & Skills
- Strong experience in international regulatory affairs.
- Expertise in regulatory documentation and dossier preparation.
- Knowledge of CTD/eCTD submission formats.
- Understanding of global regulatory compliance requirements.
- Experience with pharmaceutical product registrations.
- Excellent documentation and project management skills.
- Strong communication and stakeholder management abilities.
- Familiarity with Regulatory Information Management Systems (RIMS) is an added advantage.
Why Join Tanishq Life Care?
- Opportunity to work on international regulatory submissions.
- Exposure to multiple global pharmaceutical markets.
- Collaborative cross-functional work environment.
- Career growth in pharmaceutical regulatory affairs.
- Work with a respected and expanding pharmaceutical company.
- Gain experience in international compliance and product lifecycle management.
Salary and Benefits
Based on current pharmaceutical industry standards in Ahmedabad, the estimated salary for this position is:
₹5.5 LPA – ₹9.5 LPA
Additional benefits may include:
- Performance-based incentives
- Professional development opportunities
- Regulatory training programs
- Career advancement opportunities
- Employee-friendly work culture
How to Apply
Interested and eligible candidates can apply by sending their updated resume to:
Email: export@tanishqlifecare.com