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Regulatory Affairs Jobs at Vivanza Biosciences 2026
Published on: September 19, 2026
Vivanza Biosciences has a Regulatory Affairs opening in Ahmedabad, Gujarat. The available vacancy details mention 5 openings for candidates with 1–5 years of relevant experience.
The position involves regulatory documentation, product registration, ACTD/CTD dossier preparation, CMC-related documentation, stability information, artwork review and regulatory submissions for international markets.
1. Vivanza Biosciences Regulatory Affairs Job Overview
| Particular | Details |
|---|---|
| Company | Vivanza Biosciences |
| Position | Regulatory Affairs |
| Location | Ahmedabad, Gujarat |
| Experience | 1–5 years |
| Vacancies | 5 |
| Qualification | B.Pharm / M.Pharm or equivalent |
| Job Type | Full-time |
| Work Area | Pharmaceutical Regulatory Affairs |
| Salary | Not specified |
| Official Careers Page | Vivanza Biosciences Careers |
Important: The available vacancy details mention 1–5 years of relevant experience. Freshers should confirm their eligibility directly with the company before applying.
2. Key Responsibilities
The position is mainly related to regulatory documentation, product registration and coordination of submission-related activities.
| Area | Work Involved |
|---|---|
| Regulatory Dossiers | Preparation and handling of ACTD/CTD dossiers |
| Technical Documentation | COA, MFR, validation and related documents |
| Stability | Preparation or review of stability information |
| Artwork | Review and coordination of product artwork |
| CMC | Support for Chemistry, Manufacturing and Controls documentation |
| Product Registration | Supporting registration and submission activities |
| International Markets | Regulatory activities for Africa, LATAM, CIS and other emerging markets |
| Coordination | Coordination with relevant teams and management |
In practical terms, the role involves working with regulatory and technical documents needed for product registration. Depending on the assigned products and markets, the person may collect information from different departments, review supporting documents and assist with regulatory submissions.
3. ACTD, CTD and CMC Mentioned in the Vacancy
Some of the technical areas mentioned in the vacancy are:
- CTD: Common Technical Document used to organize regulatory information for submissions.
- ACTD: ASEAN Common Technical Dossier used for regulatory submissions in ASEAN markets.
- CMC: Chemistry, Manufacturing and Controls information covering the product, manufacturing process and quality aspects.
- COA: Certificate of Analysis.
- MFR: Master Formula Record.
These areas are particularly relevant to professionals who have experience with dossier preparation, product registration or regulatory submissions.
4. International Markets
The vacancy refers to regulatory activities for several international market groups.
| Market | Regulatory Work |
|---|---|
| Africa | Product registration and regulatory documentation |
| LATAM | Regulatory submissions and registration |
| CIS | Regulatory documentation and registration |
| Other Emerging Markets | Market-specific regulatory activities |
If you have previous international regulatory experience, it is better to mention the specific countries, products or projects you have actually worked on rather than using a general term such as “international experience.”
5. Eligibility
The available vacancy details mention the following requirements:
- B.Pharm, M.Pharm or equivalent qualification
- 1–5 years of relevant experience
- Experience in pharmaceutical Regulatory Affairs
- Familiarity with regulatory documentation and submission-related activities
Since recruitment requirements can change, candidates should verify the latest requirements with the company before applying.
6. What to Highlight on Your CV
If your experience matches the position, you can highlight the regulatory activities you have actually handled.
| Area of Experience | What You Can Mention |
|---|---|
| Dossier Preparation | ACTD/CTD dossier compilation or preparation |
| Product Registration | Registration submissions and supporting documents |
| Regulatory Submissions | Submission preparation, tracking or responses |
| CMC | CMC documentation and coordination |
| Stability | Stability data preparation or review |
| Artwork | Regulatory artwork review or coordination |
| International Markets | Specific countries or markets handled |
| Variations/Renewals | Variation or renewal activities handled |
Do not add regulatory activities to your CV simply because they are mentioned in the job description. Mention only the work, skills or projects you have actually handled.
7. Salary and Employment Details
The available vacancy information does not specify the salary.
Candidates should confirm the CTC, benefits, working hours, notice-period requirements and other employment terms directly with the company before accepting an offer.
8. About Vivanza Biosciences
For more information about the company and its career opportunities, candidates can visit the official website:
Vivanza Biosciences Careers:
Official Careers Page
9. How to Apply
According to the available vacancy details, candidates can send their resume to:
Email: business@vivanzabiosciences.com
Subject: Regulatory Affairs
Before applying, make sure your resume clearly presents your qualification, relevant Regulatory Affairs experience, markets handled and technical areas you have actually worked on.
10. Frequently Asked Questions
How many Regulatory Affairs vacancies are available at Vivanza Biosciences?
The available vacancy details mention 5 openings.
What qualification is required?
The listed qualification is B.Pharm, M.Pharm or equivalent.
How much experience is required?
The stated experience range is 1–5 years of relevant Regulatory Affairs experience.
Which regulatory areas are mentioned in the vacancy?
The vacancy mentions ACTD/CTD dossiers, CMC documentation, stability information, artwork, product registration and regulatory submissions.
Is the salary mentioned?
No. The available vacancy details do not specify the salary.
Is this vacancy suitable for freshers?
The vacancy is listed for candidates with 1–5 years of relevant experience. Freshers should confirm with Vivanza Biosciences whether applications from candidates without prior industry experience are being considered.
11. Related Regulatory Affairs Resources
If you are looking for more information about Regulatory Affairs careers and opportunities, you can also explore:
Important Note
Recruitment details such as vacancies, eligibility, salary and application status can change. Candidates should verify the latest information with Vivanza Biosciences before applying.
PharmaCareerUpdates.com is an independent career information website and is not affiliated with Vivanza Biosciences. Never pay anyone to secure a job or interview.
Final Thoughts
The Vivanza Biosciences Regulatory Affairs opportunity may be relevant for B.Pharm and M.Pharm professionals who have experience in regulatory documentation, product registration, dossier preparation or international submissions.
Before applying, check the latest vacancy information and make sure the position matches your qualification and actual work experience.
