Troikaa Pharma is inviting applications for Regulatory Affairs professionals through a walk-in interview scheduled in March 2026. The company is looking for experienced candidates with expertise in dossier preparation, CTD/ACTD documentation, and regulatory submissions for global markets.
Troikaa Pharma is known for innovation in pharmaceutical products and drug delivery systems. With a presence in more than 90 countries and advanced manufacturing facilities in India, the company offers strong career opportunities for regulatory professionals who want to work in global pharmaceutical markets.
Candidates with M.Pharm qualification and relevant regulatory affairs experience are encouraged to register for the walk-in process.
Author: Pharmabharat Editorial Team
About Troikaa Pharma
Troikaa Pharma is a leading pharmaceutical company recognized for its innovative research and development capabilities. The companyโs NDDS brands such as Dynapar AQ and Dynapar QPS have significantly contributed to advancements in pain management.
Troikaa operates modern manufacturing facilities in Thol, Dehradun, and Sanand, which are accredited by global regulatory authorities including EU, WHO, PIC/S, ANVISA Brazil, and INVIMA. The company employs a diverse workforce representing more than 90 countries.
Job Details
Position: Sr Officer / Executive โ Regulatory Affairs
Experience Required: 3+ Years
Qualification: M.Pharm
Job Location: Ahmedabad, Gujarat (Exact location shared with registered candidates)
Available Roles
ROW Market Regulatory Affairs
Candidates will work on regulatory documentation and submissions related to ROW (Rest of World) markets.
US / Europe Market Regulatory Affairs
Candidates will support regulatory documentation and dossier preparation for regulated markets including the United States, Europe, UK, and Brazil.
Roles and Responsibilities
Candidates selected for the Regulatory Affairs position will be responsible for:
- Preparing regulatory dossiers and documentation
- Handling CTD and ACTD format submissions
- Reviewing and compiling regulatory documents
- Managing document requisition and regulatory compliance requirements
- Supporting product registration in global markets
- Coordinating with internal departments for regulatory submissions
- Ensuring adherence to country-specific regulatory guidelines
Required Qualifications
Applicants must meet the following eligibility criteria:
- Educational Qualification: M.Pharm (Master of Pharmacy)
- Experience: Minimum 3 years in Regulatory Affairs
- Experience in Dossier Preparation, CTD, ACTD documentation
- Knowledge of country-specific regulatory requirements
- Experience with ROW, US, Europe, UK or Brazil regulatory markets
Salary and Benefits
Troikaa Pharma offers competitive compensation packages for qualified candidates.
- ROW Market Role: Up to โน5 LPA CTC
- US / Europe Market Role: Up to โน6 LPA CTC
Additional benefits may include:
- Career growth opportunities in global regulatory markets
- Exposure to international pharmaceutical regulations
- Professional development within a reputed pharmaceutical company
Walk-In Interview Details
Interview Date: 14 March 2026 (Saturday)
Time: 10:00 AM onwards
Location: Will be shared with registered candidates only
The company prefers immediate joiners for these positions.
How to Apply
Interested candidates must register for the interview through the registration link mentioned in the official job notification.
Steps to apply:
- Register using the official application link provided by the company
- Wait for confirmation from the recruitment team
- The interview location will be shared after successful registration
- Carry updated resume and relevant documents for the interview
