Piramal Regulatory Affairs hiring is open now for the Executive position, Interested candidates may Apply Now.
Company Profile:
The Consumer Products Division at Piramal is a standout business arm of Piramal Pharma Limited, dedicated to addressing everyday consumer needs. Since its inception in 2009, Piramal CPD has remained committed to putting customers first and resolving common challenges. Being a part of the long-established Piramal Group for over 38 years, we take pride in our heritage built upon the pillars of Knowledge, Action, Care, and Impact. These values define our organizational ethos, guiding how we function. Our mission revolves around ‘Doing Well and Doing Good,’ a philosophy that has positively impacted the lives of over 70 million Indians through the Piramal Consumer Products Division. Read all Piramal Regulatory Affairs Hiring details as given below.
Piramal Regulatory Affairs Job Overview
| Company | Piramal |
| Industry Type | Pharma/ Healthcare/ Clinical research |
| Functional Area | Regulatory Affairs |
| Post | Executive Regulatory Affairs |
| Experience | 2-5 years |
| Qualification | M.Sc, B.Sc, B.Pharma |
| Location | Mumbai, Maharashtra |
| End Date | 25th January, 2024 |
| Apply Online | Apply here |
| Check Other Jobs | Regulatory Jobs |
Piramal Regulatory Affairs Hiring Description
- Regulations and Compliance
- Execute tasks as per SOP and work process
- Read and understand all regulatory requirements as per business needs
- Stay updated on new regulations
- Liaise with internal stakeholders to ensure OTIF delivery of projects
Regulatory Review
- Documents Review as per regulatory compliance
- Conduct a review of artworks of assigned products
- Conduct review of labels, pack inserts, promotional material – banners, leaflets, print ads,
- TVC, social media campaigns of assigned products
- Support marketing in evaluating NPDs of assigned projects
- Exports, Institutional Sales & E-commerce
- Search, read, and understand the regulatory requirements of export markets
- Prepare product dossiers for registration
- Provide all regulatory documents promptly Archive all submissions Update and maintain the status of regulatory filings
- Ensure regulatory compliance in export markets post-registration
Documentation
- Maintain a repository of regulatory and scientific documents
- Maintain tracker for trademarks, artworks, promotional material, exports, institutional sales
- Archive all regulatory correspondence
Candidate Profile
- MSc (Life Science/ Biology/ Biochem/ Molecular Biology) OR BSc (Life-Sciences/ Biochem /Biotech)/BPharm
- Well-versed with regulations such as FSSAI, D&C Act, DMR Act, BIS, Legal Metrology
- Has a good understanding of the operational processes of FSSAI, DCGI, and other regulatory bodies
- Previous regulatory experience in drugs and/or nutraceutical
- Ability to critically review manufacturing, pharmacology, pre-clinical and clinical data, reports, literature and documentation
- Interact and maintain relations with cross-functional team
- Ability to independently manage assigned tasks
- Basic IT knowledge