Regulatory Affairs Jobs at Piramal | Candidates | Apply Now
Are you looking for Regulatory Affairs Jobs in a leading global pharmaceutical company? Explore exciting Executive Jobs through Piramal Careers for the position of Executive – Regulatory Affairs in Navi Mumbai. This full-time, on-site opportunity offers hands-on experience in regulatory submissions, database management, and coordination with the FDA and CDSCO, making it an excellent career move for chemistry graduates seeking growth in the pharma industry.
About Piramal Pharma Limited
Piramal Pharma Limited offers a portfolio of differentiated products and services through its 17 global development and manufacturing facilities and a global distribution network in over 100 countries. The company operates through multiple business verticals, including Piramal Pharma Solutions (PPS), an integrated Contract Development and Manufacturing Organization; Piramal Critical Care (PCC), a Complex Hospital Generics business; and the India Consumer Healthcare business, selling over-the-counter products. One of its associate companies, AbbVie Therapeutics India Private Limited, is a JV with AbbVie Inc. and has emerged as one of the market leaders in the ophthalmology therapy area. Further, PPL has a minority investment in Yapan Bio Private Limited. In October 2020, PPL received a 20% strategic growth investment from The Carlyle Group. Start
your journey in Regulatory Affairs Jobs today by applying through Piramal Careers and grow your future with one of the leading pharmaceutical organizations offering promising Executive Jobs in India.Job Overview
Explore Regulatory Affairs Jobs through Piramal Careers for the position of Executive – Regulatory Affairs based in Navi Mumbai. This is a full-time, onsite opportunity ideal for candidates seeking Executive Jobs in the pharmaceutical sector.
- Department: Regulatory Affairs
- Location: Navi Mumbai
- Job Type: Full-time
- Travel: Low
- Job Requisition ID: 10236
The role involves maintaining regulatory databases, supporting document compilation, and coordinating required documentation for regulatory submissions, amendments, and license applications with the FDA and CDSCO. The position also includes preparing Letters of Access and performing other duties as assigned by the Head of Department.
Key Responsibilities
- Maintaining and updating the database to track the submissions.
- Support for document compilation for the Applicant’s part.
- Preparation of Letter of Access.
- Collection of documents for Annual updates, Amendments, and CEP Amendments.
- Collection of documents for License applications to the FDA and the CDSCO.
- Any other work assigned by HOD/Designee.
This opportunity under Piramal Careers provides valuable exposure to regulatory compliance processes and is ideal for professionals aiming to build long-term careers in Regulatory Affairs Jobs within the pharmaceutical industry.
Preferred Candidate Profile
- Master’s/bachelor’s degree in chemistry or a related field.
- Basic understanding of peptide synthesis principles is a plus.
- Strong attention to detail and commitment to quality.
- Ability to work in a team-oriented environment.
- Good communication and interpersonal skills.
- Willingness to learn and adapt to new processes.
Essential Qualification
Master’s/bachelor’s degree in chemistry or a related field (Full-time).
