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If you are searching for Drug Regulatory Affairs jobs in India with exposure to global regulatory submissions, Evolet Healthcare Pvt. Ltd. has opened exciting opportunities for DRA Executive / Senior Executive professionals at its Gurugram office. This role is ideal for candidates who want hands-on experience in CTD/ACTD dossier preparation, ICH guidelines, and multi-country regulatory markets such as CIS, ASEAN, LATAM, and Africa.
With the pharmaceutical industry rapidly expanding into international markets, regulatory professionals are in high demand—and this opening offers a strong platform for long-term career growth in regulatory affairs.
Evolet Healthcare Pvt. Ltd. is a growing pharmaceutical organization focused on delivering quality medicines to regulated and semi-regulated global markets.
Headquarters: Gurugram, Haryana, India
Founded: Around 2014 (approx.)
Employees: 200+ professionals
Business Presence: CIS, ASEAN, LATAM, African markets
Evolet Healthcare is known for its strong regulatory compliance culture, emphasis on ICH and GMP standards, and continuous expansion into international pharmaceutical markets. The company encourages learning, ownership, and long-term professional stability.
Evolet Healthcare is hiring Drug Regulatory Affairs Executive / Senior Executive professionals with 2–6 years of experience to manage end-to-end regulatory submissions. The role involves preparing CTD/ACTD dossiers, responding to MOH queries, handling product lifecycle management, and coordinating with manufacturing plants for global registrations.
This is a full-time, on-site role at the Gurugram office, offering excellent exposure to international regulatory frameworks.
Position: Drug Regulatory Affairs Executive / Senior Executive
Department: Regulatory Affairs
Job Location: Gurugram, Haryana
Experience Required: 2–6 Years
Employment Type: Full-Time
Industry: Pharmaceutical / Regulatory Affairs
As a DRA Executive or Senior Executive at Evolet Healthcare, your role will focus on ensuring that pharmaceutical products meet global regulatory requirements. Key responsibilities include:
Preparing and reviewing CTD & ACTD dossiers for new registrations and renewals
Managing product life cycle management (PLCM) activities
Handling regulatory submissions from start to approval stage
Coordinating with internal teams, QA, QC, and manufacturing plants
Responding to MOH queries within committed timelines
Working on country-specific regulatory guidelines
Supporting registrations in CIS, ASEAN, LATAM, and African markets
Ensuring compliance with ICH guidelines and GMP practices
Assisting in regulatory audits and inspections
Providing regulatory training and guidance to junior team members
Traveling to manufacturing sites when regulatory coordination is required
This role demands accuracy, documentation expertise, and the ability to manage multiple regulatory projects simultaneously.
UG: B.Pharm (Any Specialization)
PG: M.Pharm (Any Specialization)
Minimum 2 to 6 years of hands-on experience in Drug Regulatory Affairs
Strong experience with CTD/ACTD formats
In-depth knowledge of ICH guidelines
To succeed in this role, candidates should have:
Strong understanding of global regulatory submissions
Excellent documentation and analytical skills
Working knowledge of GMP and compliance systems
Ability to interpret regulatory data logically
Capability to manage multiple dossiers and deadlines
Proficiency in MS Word, Excel, Email, and Internet tools
Strong English communication skills (written & verbal)
Detail-oriented, proactive, and systematic work approach
Based on current pharma regulatory industry standards:
Estimated CTC: ₹6,00,000 – ₹10,00,000 per annum
Final salary will depend on experience, regulatory exposure, and interview performance.
Interview Mode: HR + Technical (Regulatory) rounds
Interview Location: Gurugram / Virtual (as per company decision)
Shortlisting: Resume-based shortlisting only
Shortlisted candidates will be contacted directly by the HR team.
Candidates should keep the following documents ready:
Updated resume/CV
Educational certificates (B.Pharm/M.Pharm)
Experience letters and current CTC proof
ID proof (Aadhaar/PAN)
Passport (if available – preferred for global regulatory roles)
Gurugram, Haryana
This is an on-site role with occasional travel to manufacturing locations.
Interested and eligible candidates can apply by email:
π§ Send CV to: vacancy@evolet.in
π Subject Line: Application for DRA Executive / Sr Executive
Apply early to increase your chances of shortlisting.
Q1. Who can apply for this DRA role at Evolet Healthcare?
Candidates with 2–6 years of experience in Drug Regulatory Affairs and CTD/ACTD dossiers can apply.
Q2. Is this role suitable for freshers?
No, this position requires prior regulatory experience.
Q3. Which markets will I work on?
CIS, ASEAN, LATAM, and African regulatory markets.
Q4. Is travel required in this role?
Yes, occasional travel to manufacturing plants may be required.
Q5. What is the job location?
Gurugram, Haryana.
The Drug Regulatory Affairs Executive / Sr Executive opening at Evolet Healthcare Pvt. Ltd. is an excellent opportunity for regulatory professionals seeking global exposure, career stability, and long-term growth. If you want to work on international dossiers and strengthen your regulatory expertise, this role can be a strong next step in your pharma career.
Note: Pharma Duniya does not charge any money for job information.
Candidates are advised to verify details from the official company website.
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