Executive - Regulatory Affairs

Roles and Responsibilities
To arrange administrative documents required for dossier submission & export purpose

(Manufacturing Lic, WHO-GMP, P.P/COPPs/FSC- Procuring and legalization).
To check & approve the artworks for regulated / semi regulated countries.
To Co-ordinate and follow-up with manufacturer for documents & samples/WS required for regulatory submission.
Handling queries pertaining to regulatory submissions from various regulatory authorities.
Maintain record of samples, shade cards, registration certificate etc.

Desired Skills
Should have positive communication skill.
Good technical knowledge, review skills, and understanding of regulatory submissions.
Valuable leadership and organizational skills, with a strong focus on execution and follow-through.

Work Experience:
Work experience: 3 - 5 years’ experience in regulatory affairs.

Industry Type: Pharmaceutical & Life Sciences

Department: Legal & Regulatory

Education

B.Pharma in Pharmacy, M.Pharma in Pharmacy





COMPANY NAME:
Lavina Pharmaceuticals Pvt. Ltd.

COMPANY PROFILE:
Lavina Pharmaceuticals Pvt. Ltd. Was established in the year 2004. We are the supplier and the Exporter of Pharmaceutical Formulation like Tablets, Capsules, Injectable, Creams, Infusion, and Liquids, Pharmaceuticals Intermediates, Pharmaceutical chemicals, Inorganic capsules, We are mainly involved in supplying our several range of pharmaceutical forms in East African, West Africa and Southwestern Asia, Southeast Asia,. Lavina Pharmaceuticals Pvt Ltd covers all product range like anti-infectives, anti
inflammatory and the arthritis, Cardiovascular, oncology, anti-diabetic, gastrointestinal and cough expectorant, multivitamin toxics.

Company Website:
Job Types: Full time, Permanent

Pay: ₹30,000.00 - ₹40,000.00 per month

Benefits:
Provident Fund

Work Location: In person

📌 Executive Regulatory Affairs Vashi (India)
🏢 LAVINA PHARAMACEUTICALS
📍 India