
About the Organisation
Zolvit is your one-stop platform for SMB legal, tax, and compliance needs. With the highest industry rating and over 14,500+ satisfied Google reviews with a 4.4 rating, we ensure quality and reliability across 350+ services. Our team of 500+ experts guarantees timely assistance, backed by our self-service DIY proprietary automation platform. Trusted by 5 lac+ businesses globally, we partner with industry leaders like Meesho, Amazon, Flipkart, Kotak Bank, and more.
Role Overview
We are seeking experienced Advocates to join our in-house legal team in Noida to handle ongoing matters related to pharmaceutical regulations. The role requires professionals with prior exposure to pharmaceutical company legal matters, including regulatory frameworks under the Drugs and Cosmetics Act and a basic understanding of NDPS provisions.
Key Responsibilities
- Handle legal matters related to pharmaceutical regulations and compliance.
- Manage cases and legal proceedings under the Drugs and Cosmetics Act and related regulatory laws.
- Assist in handling matters involving NDPS provisions where applicable.
- Coordinate with external counsel and represent the organization before regulatory authorities and courts when required.
- Draft and review legal documents, responses, and submissions to regulatory bodies.
- Provide legal advice to internal stakeholders on regulatory and compliance matters related to pharmaceutical operations.
- Track ongoing cases and ensure timely legal filings and documentation.
Required Qualifications & Skills
- LLB from a recognized university; enrollment with the Bar Council is mandatory.
- 3-4 years of relevant legal experience.
- Prior exposure to pharmaceutical industry matters or regulatory litigation.
- Good understanding of the Drugs and Cosmetics Act and basic familiarity with NDPS-related provisions.
- Strong legal drafting, research, and analytical skills.
- Ability to manage multiple legal matters and coordinate with stakeholders.
Preferred Background
Experience working with pharmaceutical companies, regulatory litigation, or law firms handling pharma compliance matters.
Exposure to government regulatory authorities related to pharmaceutical compliance.

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