Tashi Pharma is inviting applications for the position of Regulatory Affairs Executive in Ahmedabad, Gujarat. According to the available vacancy listing, the company has 2 openings for candidates interested in pharmaceutical regulatory affairs, dossier preparation, and product registration for international markets.
Both freshers and experienced candidates can apply. A bachelor’s degree in Pharmacy is preferred, while M.Pharm or a relevant Life Sciences qualification may provide an additional advantage. Candidates familiar with CTD/ACTD dossier preparation, pharmaceutical registration documents, and export-market regulatory requirements may be particularly suitable for this opportunity.
This position offers an opportunity to work with regulatory documentation for Latin American (LATAM), Southeast Asian, and Rest of the World (ROW) markets.
Tashi Pharma Recruitment 2026: Job Highlights
| Particulars | Details |
|---|---|
| Company | Tashi Pharma |
| Job Title | Regulatory Affairs Executive |
| Job Location | Ahmedabad, Gujarat |
| Number of Openings | 2 |
| Experience | Freshers and experienced candidates |
| Preferred Qualification | Bachelor’s degree in Pharmacy |
| Additional Qualifications | M.Pharm or relevant Life Sciences qualification |
| Job Category | Pharmaceutical Regulatory Affairs |
| Key Skills | CTD/ACTD dossiers, regulatory documentation, product registration |
| Salary | Not specified in the available vacancy details |
| Application Mode | |
| Application Email | hr@tashipharma.com |
About Tashi Pharma Recruitment
Tashi Pharma is seeking candidates for regulatory affairs activities related to pharmaceutical product registrations in international markets. The role involves preparing regulatory dossiers, collecting technical documents from internal departments, maintaining accurate records, and supporting country-specific registration requirements.
Applicants interested in building a career in pharmaceutical regulatory affairs may consider this opportunity, particularly if they have an academic background in Pharmacy or Life Sciences.
Job Description: Regulatory Affairs Executive
The Regulatory Affairs Executive will support the preparation, compilation, review, and maintenance of pharmaceutical registration dossiers and associated technical documents.
The role involves coordinating with departments such as Quality Assurance, Quality Control, and Manufacturing to obtain the information required for product registrations. The candidate will also help ensure that documentation is complete, consistent, and aligned with applicable country-specific regulatory requirements.
Key Responsibilities
1. Regulatory Dossier Preparation
- Prepare, compile, and review pharmaceutical registration dossiers in CTD or ACTD formats, as applicable.
- Maintain regulatory documentation for LATAM, Southeast Asian, and ROW markets.
- Organize supporting documents required for pharmaceutical product registration.
- Review dossiers for completeness, accuracy, consistency, and compliance with relevant guidelines.
2. Technical Documentation Coordination
- Coordinate with QA, QC, Manufacturing, and other departments to collect required technical information.
- Compile product specifications, Certificates of Analysis (CoAs), and manufacturing documentation.
- Maintain stability data, analytical methods, GMP certificates, and other supporting records.
- Follow up with relevant teams to obtain missing or updated documents.
3. Country-Specific Registration Requirements
- Prepare or compile application forms, declarations, undertakings, and supporting documents.
- Assist with country-specific registration and submission requirements.
- Support document legalisation, notarisation, apostille, or certification processes where applicable.
- Help maintain documentation according to the requirements of the target market.
4. Regulatory Updates and Document Control
- Monitor changes in country-specific regulatory requirements.
- Communicate relevant regulatory updates to the team.
- Maintain organized and accurate regulatory records.
- Support timely completion of assigned dossier-related tasks.
Eligibility Criteria
Educational Qualification
Candidates with the following qualifications may apply:
- B.Pharm – Bachelor of Pharmacy.
- M.Pharm – Master of Pharmacy.
- Relevant Life Sciences qualification.
A bachelor’s degree in Pharmacy is listed as the preferred qualification. M.Pharm and relevant Life Sciences qualifications are described as additional advantages.
Experience Required
Both freshers and experienced candidates are eligible to apply according to the vacancy listing.
Previous experience in pharmaceutical Regulatory Affairs, especially export-market registration, is preferred but is not presented as mandatory for every applicant.
Required Skills
Candidates should ideally have:
- Knowledge of pharmaceutical regulatory documentation.
- Familiarity with CTD and ACTD dossier structures.
- Understanding of pharmaceutical product registration requirements.
- Knowledge of product specifications, CoAs, stability data, and GMP documentation.
- Strong written and verbal communication skills.
- Attention to detail and document accuracy.
- Good organizational and time-management skills.
- Ability to manage multiple documents and deadlines.
- Proficiency in Microsoft Word and Excel.
Job Location
The position is based in Ahmedabad, Gujarat, India.
Candidates should confirm the exact office location, work schedule, and other employment conditions with the recruitment team.
Salary and Benefits
The salary package and employee benefits have not been specified in the available vacancy details. Applicants can contact the recruitment team to confirm compensation, working hours, benefits, and other employment terms.
How to Apply for Tashi Pharma Recruitment 2026
Interested candidates can send their updated resume to the recruitment email address provided in the vacancy announcement.
Company: Tashi Pharma
Position: Regulatory Affairs Executive
Location: Ahmedabad, Gujarat
Openings: 2
Email: hr@tashipharma.com
Application Tips
- Prepare an updated resume with your educational qualifications and relevant skills.
- Mention Regulatory Affairs Executive Application in the email subject line.
- Highlight any academic projects, training, internships, or experience related to pharmaceutical regulatory affairs.
- Mention familiarity with CTD/ACTD dossiers and export-market registration, if applicable.
- Attach your resume in PDF format and ensure your contact details are correct.
Frequently Asked Questions (FAQs)
1. Which company is hiring for Regulatory Affairs Executive jobs?
Tashi Pharma is listed as the recruiting company.
2. Where is the job located?
The vacancy is based in Ahmedabad, Gujarat.
3. How many vacancies are available?
The available listing mentions 2 openings.
4. Can freshers apply?
Yes. Both freshers and experienced candidates are eligible according to the vacancy listing.
5. What qualification is preferred?
A bachelor’s degree in Pharmacy is preferred. M.Pharm or a relevant Life Sciences qualification may also be considered.
6. What are the main responsibilities?
The role involves regulatory dossier preparation, technical document coordination, product registration documentation, and support for country-specific regulatory requirements.
7. What are CTD and ACTD dossiers?
CTD stands for Common Technical Document, while ACTD stands for ASEAN Common Technical Dossier. These formats organize technical information used in pharmaceutical registration submissions in relevant markets.
8. Is export-market experience mandatory?
The vacancy description identifies pharmaceutical Regulatory Affairs experience, particularly in export markets, as preferred. It also states that freshers can apply.
9. What is the salary for this position?
The salary has not been disclosed in the available vacancy information.
10. How can candidates apply?
Candidates can email their updated resume to hr@tashipharma.com.
Disclaimer
This article is a rewritten summary of a third-party vacancy listing. Vacancy availability, eligibility criteria, compensation, and application instructions may change. Candidates should verify the latest details with Tashi Pharma before applying.