Tashi Pharma is hiring two candidates for the position of Regulatory Affairs Executive in Ahmedabad, Gujarat.
The opportunity is open to freshers and experienced professionals interested in pharmaceutical regulatory affairs and product registration.
Candidates with a B.Pharm, M.Pharm, or a relevant life sciences qualification can apply, with prior regulatory affairs experience preferred.
Interested applicants can send their updated resumes to the company’s recruitment email address.
Company Overview
Tashi Pharma is inviting applications for its Regulatory Affairs department. The role involves preparing pharmaceutical registration dossiers, maintaining regulatory documentation, coordinating with internal departments, and supporting product registrations across international markets.
Tashi Pharma Regulatory Affairs Executive Job Details
Position Information
- Company: Tashi Pharma
- Department: Regulatory Affairs
- Designation: Regulatory Affairs Executive
- Number of Openings: 2
- Job Location: Ahmedabad, Gujarat
- Experience: Freshers and experienced candidates can apply
Job Role & Responsibilities
The selected candidates will support pharmaceutical regulatory documentation, dossier preparation, and registration activities.
Key Responsibilities
- Prepare, compile, and review pharmaceutical registration dossiers in CTD and ACTD formats, as applicable.
- Prepare and maintain regulatory dossiers and supporting documents for LATAM, Southeast Asian, and Rest of World (ROW) markets.
- Coordinate the collection of technical documents from Quality Assurance (QA), Quality Control (QC), Manufacturing, and other internal departments.
- Compile and maintain product specifications, Certificates of Analysis (CoAs), manufacturing details, stability data, analytical methods, GMP certificates, and other regulatory documents.
- Prepare and manage country-specific regulatory documentation, application forms, declarations, undertakings, and supporting documents required for product registration.
- Review dossiers for completeness, accuracy, consistency, and compliance with applicable regulatory guidelines and market-specific requirements.
- Assist with the legalization, notarization, apostille, and certification of regulatory documents wherever required.
- Monitor changes in country-specific regulatory requirements and communicate their potential impact to the team.
Eligibility & Qualifications
Educational Qualifications
- B.Pharm is preferred.
- M.Pharm is also relevant.
- Candidates with other relevant life sciences qualifications may be considered.
Experience Requirements
- Freshers can apply.
- Experienced candidates with pharmaceutical regulatory affairs experience will be preferred.
- Experience in export markets and pharmaceutical registration activities is an advantage.
Required Skills
- Knowledge of CTD and ACTD dossier preparation.
- Understanding of pharmaceutical registration documentation.
- Familiarity with GMP certificates, CoAs, product specifications, stability data, and manufacturing documentation.
- Good written and verbal communication skills.
- Strong organizational skills and attention to detail.
- Ability to manage multiple regulatory dossiers and deadlines.
- Proficiency in Microsoft Office, particularly Word and Excel.
Location & Salary
Job Location
Ahmedabad, Gujarat, India.
Salary Details
The salary package has not been specified in the recruitment announcement. Compensation may depend on the candidate’s qualifications, skills, and relevant experience.
How to Apply
Interested candidates can apply for the Regulatory Affairs Executive position by emailing their updated resume to the recruitment team.
Email: hr@tashipharma.com
Application Instructions
- Prepare an updated resume highlighting relevant pharmaceutical or life sciences qualifications.
- Include any experience in regulatory affairs, CTD/ACTD dossiers, pharmaceutical documentation, or product registration.
- Send the resume to the recruitment email address provided above.
Important Details
- A total of two vacancies are available.
- Both freshers and experienced candidates are eligible to apply.
- Candidates with pharmaceutical regulatory affairs experience, particularly in export markets, will be preferred.
- Knowledge of regulatory documentation and Microsoft Office is relevant to the role.
Frequently Asked Questions
1. What is the designation offered at Tashi Pharma?
The advertised position is Regulatory Affairs Executive.
2. How many vacancies are available?
There are two openings for the Regulatory Affairs Executive position.
3. Are freshers eligible to apply?
Yes. Freshers can apply, although candidates with prior pharmaceutical regulatory affairs experience will be preferred.
4. What qualifications are required?
B.Pharm is preferred. M.Pharm and relevant life sciences qualifications may also be considered.
5. Where is the job located?
The position is based in Ahmedabad, Gujarat.
6. How can candidates apply?
Candidates can email their updated resumes to hr@tashipharma.com.
Job Summary
| Category | Details |
|---|---|
| Company | Tashi Pharma |
| Vacancies | Regulatory Affairs Executive: 2 openings |
| Required Education | B.Pharm preferred; M.Pharm or relevant life sciences qualification |
| Experience | Freshers and experienced candidates |
| Location | Ahmedabad, Gujarat |