Join the Team
Careers at Advocate Srijan Tiwari — Delhi's Drug Law Practice
We are a small, intensely focused team. Every position here is for someone who wants to become India's best in drug and cosmetics law — not someone looking for a stepping stone.
Why Join Us
What Makes This Practice Different to Work At
There are thousands of law firms in Delhi. Here is why serious legal professionals choose to build their careers at this one.
Depth Over Breadth
We do one thing — drug and cosmetics law — and we do it exceptionally. Everyone here becomes a genuine specialist, not a generalist who dabbles.
Direct Mentorship
Junior advocates work directly with Advocate Srijan Tiwari — not through layers of seniority. You learn from the best, directly.
Corporate-Grade Exposure
Our clients are India's leading pharmaceutical corporations. The standard of work — and the learning — is correspondingly high.
Intellectual Rigour
Drug law is technical. You will be expected to understand the science behind the law. This challenge is what makes this practice genuinely interesting.
Current Openings
Open Positions — March 2026
Associate Advocate — Drug & Cosmetics Litigation
We are seeking an Associate Advocate to join our trial court and High Court litigation team. You will work directly under Advocate Srijan Tiwari on NSQ defences, regulatory prosecution matters, and Delhi High Court applications.
Key Responsibilities
- Appear in Delhi district courts for NSQ and drug prosecution matters
- Assist in drafting writ petitions, criminal appeals, and stay applications for Delhi High Court
- Review prosecution documents, government analyst reports, and form 29 data
- Conduct legal research on drug law precedents and regulatory notifications
- Attend CDSCO and state drug authority hearings as required
- Coordinate case management and client communication under senior supervision
Requirements
- LLB from a recognised Indian law school (LLM preferred)
- 1–4 years of litigation experience — drug law exposure is a strong plus
- Enrolled with Bar Council of Delhi
- Strong drafting skills in English
- Ability to work under pressure and meet tight regulatory deadlines
- Interest in pharmaceutical and regulatory law — this must be more than a job
Legal Research Associate — Drug Law
Our research team tracks all developments in drug law jurisprudence, CDSCO circulars, gazette notifications, and court judgments relevant to pharmaceutical and cosmetics regulation. We need a sharp researcher to join this function.
Key Responsibilities
- Track and summarise daily CDSCO notifications, gazette amendments, and drug law judgments
- Prepare case research memos for ongoing litigation matters
- Maintain and update the firm's internal precedent database
- Draft regulatory law updates for corporate client communications
- Assist in preparing legal opinions on drug law questions
- Research pharmacopoeial standards and testing methodology for NSQ defences
Requirements
- LLB or final year law student (law graduates preferred)
- Demonstrated interest in regulatory law, pharmaceutical law, or public health law
- Excellent written English — research outputs require clarity and precision
- Familiarity with databases such as SCC Online, Manupatra, or similar
- Strong analytical skills and attention to detail
- Ability to work independently and deliver within deadlines
Regulatory Affairs Associate
This role bridges regulatory science and legal practice. We need a professional with pharmaceutical regulatory background who can assist in technical analysis for drug law litigation — reviewing testing data, quality records, and GMP compliance for use in legal defence.
Key Responsibilities
- Analyse government analyst reports for technical deficiencies in NSQ cases
- Review pharmacopoeial testing methods and identify methodology issues for legal use
- Assist clients in preparing quality system documentation for regulatory interactions
- Provide technical inputs for show cause notice responses and regulatory hearings
- Liaise with the firm's legal team to translate technical findings into legal arguments
- Track CDSCO guidelines, BIS standards, and pharmacopoeial updates
Requirements
- B.Pharm / M.Pharm / PhD Pharmacy from a recognised institution
- 2–5 years in pharmaceutical regulatory affairs, quality assurance, or related function
- Familiarity with IP, BP, USP pharmacopoeial standards
- Experience with drug authority inspections or regulatory submissions is a strong plus
- Ability to communicate complex technical concepts clearly in writing
- Interest in working at the intersection of pharmaceutical science and law
How to Apply
Simple. Direct. No Bureaucracy.
We do not run a complex recruitment process. If you are genuinely interested in drug law and want to work at the best practice in Delhi, send us a WhatsApp message or email with:
We review all applications personally. If there is a fit, we will respond within a week. Please do not follow up before that — we respect both your time and ours.