Regulatory Affairs Specialist Vacancies in Mumbai | Ashish Life Science

Ashish Life Science Pvt. Ltd., a leader in veterinary pharmaceuticals, is currently seeking Regulatory Affairs Specialists at its Andheri West, Mumbai facility. If you have experience in dossier preparation (CTD, ACTD), handling registration queries, and coordinating with cross-functional teams for regulatory documentation, this opportunity could be your next career move.

About Ashish Life Science Pvt. Ltd.

Established in 1975, Ashish Life Science Pvt. Ltd. is a key member of the Ashish Group of Industries. Specializing in veterinary pharmaceuticals, the company has grown to become India’s largest exporter of veterinary drugs, supplying animal health solutions to over 65 countries. Ashish Life Science is known for its focus on quality, innovation, and customer satisfaction.

With a team of over 30 veterinarians globally, Ashish Life Science aims to improve animal health and well-being through innovative pharmaceutical solutions. The company prides itself on maintaining strong relationships with clients worldwide, ensuring the availability of high-quality veterinary products.

Current Opening: Regulatory Affairs Specialist

Location: Andheri West, Mumbai
Department: Regulatory Affairs

Key Responsibilities

As a Regulatory Affairs Specialist, you will be responsible for:

• Preparation of dossiers in CTD, ACTD & country specific format, renewal and variation applications for market based on region specific requirements.
• Handling registration Queries.
• Evaluation of technical documents for registration.
• Good knowledge of CTD and ACTD formats.
• Check and review of the artworks required for registration.
• Coordinating with QA ,QC and production for registration documents and samples
• Application of legal documents required for registration purpose.
• Arranging for samples for country.
• Maintain registration updates about all registration submission and approvals.

Qualifications

To be successful in this role, you should have:

• Education: A degree in Pharmacy, Life Sciences, or a related field.
• Experience: A minimum of 2-5 years of experience in regulatory affairs within the pharmaceutical industry, specifically in dossier preparation (CTD, ACTD formats) and handling registration processes.

How to Apply

Interested candidates are encouraged to apply through the company’s LinkedIn job portal