Introduction to Granules India Job Notification
Looking to build a career in the pharmaceutical industry? The latest Granules India Job Notification brings exciting opportunities for experienced professionals. Granules India, a leading pharmaceutical company, is inviting applications for the roles of Regulatory Affairs Analyst at their Hyderabad location. This post will guide you through eligibility, selection process, salary, and how to apply, all explained simply for everyone.
Overview of Granules India Job Notification
Granules India is well known for its innovative work in making and supplying high-quality medicines. Their current job are perfect for those aiming to make a meaningful impact in the pharma field, especially in supply chain management and regulatory affairs.
Granules India Job notification details
Department | : | Regulatory affairs |
Job Title | : | Analyst |
Grade | : | B |
Reporting To | : | Senior Manager |
Location | : | Granules, Gagillapur Plant Hyderabad |
Granules India Job Notification Purpose
Provide support as a team member of Regulatory affairs in supporting various works on DMF filings and Queries handling.
Granules India Job Responsibilities
- Support the compilation of Drug Master Files (DMF) and submit them to various regulatory authorities.
- Prepare dossiers following the requirements of USFDA, EDQM, ASMFs, Health Canada, WHO, and other agencies.
- Prepare responses to queries from customers and regulatory authorities.
- Evaluate change controls related to regulatory submissions.
- Prepare CEP amendments, CEP revisions, and other updates to DMFs to support product lifecycle management.
- Exposure in pharma-ready eCTD software for dossier preparation meeting regulatory standards of US, Europe, and Canada.
- Ensure PDF dossiers meet regulatory market requirements, convert PDFs to XML backbone, zip dossiers, and submit via USFDA ESG gateway and EU CESP portal.
- Coordinate with internal teams and stakeholders for smooth project management.
- Support continuous improvement in departmental procedures, practices, and compliance.
- Assist overall regulatory affairs management fostering teamwork, empowerment, and promoting values like creativity, integrity, and flexibility.
Eligibility Criteria
1) Education:
- Master’s degree or equivalent in Pharmaceutical or Chemistry or Pharmacy or Life Sciences.
2) Experience:
- 3-8 years in regulatory affairs, specifically API DMF filings.
- Candidates must have experience of working in a generic pharmaceutical company.
3) Skills:
- Knowledge and application of ICH Guidelines, DMF, EDMF / GMPs, GLPs, and GCPs principles.
Application Process
- Go to the Granules India Careers.
- Select the preferred job profile.
- Read the detailed job description carefully.
- Click on the “Apply” button.
- Fill in your details and submit the necessary documents (resume, certificates).
Conclusion
If you dream of working with a leading pharma company and helping millions access quality medicines, Granules India is looking for talents like you. Whether you’re an expert in regulatory affairs, don’t let this chance pass by. Start your journey Granules today and play a key role in India’s healthcare story.
Remember, every big career starts with a single step.
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