Regulatory Affairs Manager Jobs in Beta Drugs Ltd - Baddi, Himachal Pradesh
11 - 15 Years of Experience
Not disclosed 
Full TimeBeta Drugs Ltd
Baddi, Himachal Pradesh, India
Posted on 24-12-2025
1 Vacancy
Description
Job Requirements
- Job Title: Regulatory Affairs Manager
- Location: Beta Drugs Ltd - Baddi, Himachal Pradesh
- Work Experience: 11 to 15 Years
- Qualification: M.Pharma
Job Description
- Manage regulatory submissions for domestic and export markets.
- Prepare and review dossiers (CTD, eCTD, ACTD).
- Ensure compliance with regulatory guidelines (CDSCO, USFDA, EMA).
- Coordinate with QA, QC, and R&D for documentation.
- Handle queries, deficiencies, and regulatory correspondence.
- Manage product registrations, renewals, and variations.
- Track regulatory changes and implement updates.
- Support audits and inspections from regulatory authorities.
Take this opportunity to join Beta Drugs Ltd as a Regulatory Affairs Manager in Baddi, Himachal Pradesh and build a successful career in the healthcare industry. Apply today for this job opportunity and grow with a leading healthcare organization.
Category
Pharmaceuticals
Functional Area
Regulatory Affairs / Pharmacovigilance
Preferred Education
Key Skills
About Organization
Beta Drugs Limited is an Indian multinational pharmaceutical company known for developing, manufacturing, and marketing high-quality oncology medicines and pharmaceutical formulations. Headquartered in Panchkula, Haryana, the company operates multiple modern manufacturing facilities in India, including sites in Baddi, Himachal Pradesh, and serves customers domestically as well as in over 40 countries worldwide. Beta Drugs focuses on pharma manufacturing with a strong emphasis on oncology products, including anti-cancer tablets, capsules, injections, and APIs, while also offering contract manufacturing services and innovative formulations to improve patient care globally.
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