Regulatory Affairs Jobs at Vivanza Biosciences 2026

Vivanza Biosciences is hiring for Regulatory Affairs professionals in Ahmedabad, Gujarat. This opportunity is suitable for candidates with 1–5 years of experience in pharmaceutical regulatory activities, documentation and submission-related work.

According to the supplied job posting, the company has 5 vacancies for this full-time position. Candidates with a B.Pharma, M.Pharma or equivalent qualification can apply if they meet the requirements of the role.

Regulatory Affairs Jobs at Vivanza Biosciences 2026 – Overview

• Company: Vivanza Biosciences
• Position: Regulatory Affairs
• Location: Ahmedabad, Gujarat
• Experience: 1–5 Years
• Vacancies: 5
• Job Type: Full Time
• Qualification: B.Pharma / M.Pharma or equivalent

About the Role

The Regulatory Affairs position involves supporting pharmaceutical regulatory submissions and maintaining technical documentation required for different markets.

The selected candidate will work on regulatory documents, dossier preparation, product artwork review and coordination with regulatory authorities and internal management teams.

Key Responsibilities

The major responsibilities mentioned in the job posting include:

• Preparing Certificate of Analysis (COA) documents.
• Preparing Master Formula Records (MFR).
• Handling Product Validation (PV) documentation.
• Preparing and reviewing Stability Data.
• Developing ACTD/CTD dossiers for regulatory submissions.
• Coordinating product artwork and conducting regulatory reviews.
• Supporting CMC review and documentation.
• Working on regulatory requirements for African, LATAM, CIS and emerging markets.
• Liaising with regulatory authorities and management teams.

Eligibility and Required Skills

Candidates should have a B.Pharma, M.Pharma or equivalent qualification and 1–5 years of relevant experience.

The job posting also mentions the following requirements:

• Knowledge of ACTD/CTD dossier formats
• Familiarity with international regulatory markets
• Understanding of pharmaceutical regulatory documentation
• Good communication skills
• Strong documentation abilities
• Ability to coordinate with internal and external stakeholders

Candidates with relevant experience in regulatory submissions, CMC documentation, product validation or international pharmaceutical markets can highlight these areas in their resumes.

Regulatory Markets

The role includes regulatory activities associated with Africa, LATAM, CIS and emerging markets. Familiarity with the documentation and submission requirements of these markets can be relevant to candidates applying for the position.

This makes the opportunity particularly relevant to professionals who have already gained exposure to international regulatory affairs or pharmaceutical submissions.

Job Location

The vacancy is based in Ahmedabad, Gujarat.

Candidates interested in pharmaceutical regulatory affairs and willing to work in Ahmedabad can consider this opportunity based on their qualifications and professional experience.

Official Website

Candidates can visit the official Vivanza Biosciences website to learn more about the company and its activities.

Official Website: Vivanza Biosciences

How to Apply

Interested candidates should send their updated CV to the HR team using the email address provided in the job posting.

Email: business@vivanzabiosciences.com

Candidates should mention “Regulatory Affairs” in the email subject line.

Before applying, candidates should ensure that their CV clearly presents their educational qualifications, relevant work experience, dossier preparation knowledge and exposure to regulatory activities.

Frequently Asked Questions

What position is available at Vivanza Biosciences?

Vivanza Biosciences is hiring for a Regulatory Affairs position in Ahmedabad, Gujarat.

How many vacancies are available?

The supplied job posting mentions 5 vacancies.

What experience is required?

Candidates with 1–5 years of experience can apply.

What qualification is required?

The required qualification is B.Pharma, M.Pharma or equivalent.

Is this a full-time position?

Yes, the vacancy is listed as a Full Time position.

What regulatory markets are mentioned?

The job description mentions Africa, LATAM, CIS and emerging markets.

What knowledge is required for the role?

Candidates should have knowledge of ACTD/CTD dossier formats, regulatory documentation and international pharmaceutical markets.

How can candidates apply?

Applicants can send their updated CV to business@vivanzabiosciences.com and mention “Regulatory Affairs” in the subject line.

Disclaimer

The information published in this article is based on the job details supplied for the Vivanza Biosciences Regulatory Affairs vacancy. Job availability, vacancies, eligibility criteria and other recruitment details may change without prior notice.

Candidates should verify the latest information with the employer before applying. Pharma Career Updates is not the employer or recruitment agency and does not guarantee interview calls, selection or employment. Candidates should never make any payment to anyone in exchange for a job opportunity.