"Sqarona Medical Communications Hiring Scientific Writer & Biostatistician in Pune | Pharma Jobs 2026"

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"Sqarona Medical Communications Hiring Scientific Writer & Biostatistician in Pune | Pharma Jobs 2026" (Sqarona Medical Communications Hiring Scientific Writer & Biostatistician) Introduction If you are looking to build a long-term career in medical communications, scientific writing, or biostatistics , this is an excellent opportunity for you. Sqarona Medical Communications LLP has announced new openings for Scientific Writer (Medical Writer) and Biostatistician at its Pune (Wakad) office. With the rising demand for clinical publications, real-world evidence (RWE), and data-driven scientific content , professionals in medical writing and biostatistics are becoming highly valuable in the pharmaceutical and life sciences industry. These roles offer hands-on exposure to journals, clinical research data, publication standards, and interdisciplinary collaboration , making them ideal for early- to mid-career professionals. About The Company Sqarona Medical Communication...

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"Evolet Healthcare Hiring Drug Regulatory Affairs Executive / Sr Executive in Gurugram | Pharma Regulatory Jobs 2026"

"Evolet Healthcare Hiring Drug Regulatory Affairs Executive / Sr Executive in Gurugram | Pharma Regulatory Jobs 2026"







(Evolet Healthcare Hiring Drug Regulatory Affairs Executive / Sr Executive)







Introduction

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.


About The Company – Evolet Healthcare Pvt. Ltd.

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.


Job Overview Summary

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.


Vacancy Details (Official)

  • 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


Job Role Explanation (Responsibilities)

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.


Eligibility Criteria (Official)

Educational Qualification

  • UG: B.Pharm (Any Specialization)

  • PG: M.Pharm (Any Specialization)

Experience

  • Minimum 2 to 6 years of hands-on experience in Drug Regulatory Affairs

Regulatory Exposure

  • Strong experience with CTD/ACTD formats

  • In-depth knowledge of ICH guidelines


Skills Required 

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


Salary Estimate 

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 Details (Official)

  • 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.


Required Documents

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)


Job Location

  • Gurugram, Haryana
    This is an on-site role with occasional travel to manufacturing locations.


How to Apply 

Interested and eligible candidates can apply by email:

πŸ“§ Send CV to: vacancy@evolet.in
πŸ“Œ Subject Line: Application for DRA Executive / Sr Executive

Apply early to increase your chances of shortlisting.


FAQs – Drug Regulatory Affairs Jobs at Evolet Healthcare

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.


Final Conclusion

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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