Manager/Asst. Manager-Regulatory Affairs Jobs in Sydler Remedies Pvt Ltd - Mumbai, Maharashtra
9 - 14 Years of Experience
Not disclosed 
Full TimeSydler Remedies Pvt Ltd
Mumbai, Maharashtra, India
Posted on 15-04-2026
1 Vacancy
Description
- Job Title: Manager/Asst. Manager-Regulatory Affairs
- Qualification: BPharm/Mpharm
- Location: Sydler Remedies Pvt Ltd - Mumbai, Maharashtra
- Work Experience: 9 to 14 Years
Job Description
- Prepare and review regulatory dossiers (DMF, CEP, CTD) for API products.
- Handle submissions to regulatory authorities such as CDSCO, USFDA, EDQM, and WHO.
- Manage product registrations, renewals, and post-approval variations.
- Ensure compliance with global regulatory guidelines and standards.
- Coordinate with QA, QC, Production, and R&D teams for documentation and data.
- Review technical documents including specifications, methods, and stability data.
Take this opportunity to join Sydler Remedies Pvt Ltd - Mumbai, Maharashtra as a Manager/Asst. Manager-Regulatory Affairs in Mumbai, Maharashtra 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
Sydler Remedies Pvt. Ltd. is a pharmaceutical organization engaged in the manufacturing of high-quality formulations, nutraceuticals, herbal, and cosmeceutical products with a strong focus on regulatory compliance, product quality, and global standards. The role involves working in a manufacturing or operational environment to support production processes and ensure compliance with industry standards. Responsibilities include assisting in production activities, monitoring process parameters, maintaining accurate batch records and documentation, and ensuring adherence to safety, hygiene, and environmental guidelines. The role also requires coordination with quality assurance and quality control teams, following Good Manufacturing Practices (GMP), and contributing to consistent product quality and efficient operations.
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