Sr. Manager/Manager-Regulatory Affairs Jobs in Skymap Pharmaceuticals - Faridabad, Haryana
10 - 15 Years of Experience
Not disclosed 
Full TimeSkymap Pharmaceuticals, Faridabad
Faridabad, Haryana, India
Posted on 02-06-2026
1 Vacancy
Description
- Job Title: Sr. Manager/Manager-Regulatory Affairs
- Location: Skymap Pharmaceuticals - Faridabad, Haryana
- Work Experience: 10 to 15 Years
- Qualification: BPharm
Job Description
- Prepare, review, and submit regulatory dossiers (CTD/ACTD/eCTD) for domestic and international markets.
- Ensure compliance with regulatory requirements of authorities such as CDSCO, USFDA, MHRA, and other global agencies.
- Manage product registrations, renewals, and variations.
- Review technical documents including specifications, COA, stability data, and validation reports.
- Coordinate with QA, QC, R&D, and production teams for regulatory documentation.
Take this opportunity to join Skymap Pharmaceuticals - Faridabad, Haryana as a Sr. Manager/Manager-Regulatory Affairs in Faridabad, Haryana 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
Skymap Pharmaceuticals is a pharmaceutical company focused on developing, manufacturing, and marketing high-quality pharmaceutical formulations and healthcare products with an emphasis on innovation, regulatory compliance, and quality standards. The role involves working in a professional pharmaceutical environment to support production, quality assurance, quality control, documentation, regulatory, and operational activities. Responsibilities include maintaining GMP compliance, handling manufacturing and quality records, coordinating with cross-functional teams, monitoring production and quality processes, and supporting smooth operational workflows. The role also requires strong analytical skills, teamwork, adherence to regulatory guidelines, and commitment to delivering safe, effective, and high-quality pharmaceutical products.
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