Zenith Hiring Regulatory Executives
- Company Overview
- Job Role & Responsibilities
- Regulatory Executive – International Markets
- Eligibility / Qualifications
- Location & Salary
- Application Process
- Why Build Your Regulatory Career with Zenith Drugs
- Frequently Asked Questions (FAQs)
- How many vacancies are available?
- Is international regulatory experience mandatory?
- Which regions does this role primarily support?
- Is this role suitable for freshers?
- Does the role include foreign travel?
- Summary Table
Meta Title: B.Pharm Regulatory Executive Vacancies – Zenith Drugs Ltd
Meta Description: Zenith Drugs Ltd hiring 2 Regulatory Executives. B.Pharm mandatory, 4–6 years experience. Global regulatory exposure.
Zenith Drugs Ltd is expanding its global regulatory operations and is inviting experienced regulatory professionals who are ready to work in international pharmaceutical markets. This opportunity is ideal for candidates with strong exposure to dossier preparation, global registrations, and country-specific regulatory submissions across emerging and regulated markets. The role offers long-term growth, international exposure, and direct involvement in global healthcare product registrations.
As Zenith Drugs continues to strengthen its international footprint, this hiring reflects the company’s commitment to regulatory excellence, compliance-driven growth, and global pharmaceutical supply.
Company Overview
Zenith Drugs Ltd is an established pharmaceutical company with a growing global presence across multiple international markets. Operating with the philosophy of “Keeping Hopes Alive,” the company focuses on delivering quality-assured, affordable pharmaceutical products that meet diverse regulatory requirements worldwide.
With strong capabilities in formulation development, manufacturing, and regulatory affairs, Zenith Drugs supports product registrations across South East Asia, West Africa, LATAM, and CIS countries. The organization maintains robust regulatory systems, documentation controls, and compliance frameworks aligned with international standards.
Zenith Drugs offers professionals a structured environment to gain hands-on experience in global regulatory affairs, international tenders, and cross-functional coordination, making it a preferred employer for regulatory professionals seeking international exposure.
Job Role & Responsibilities
Regulatory Executive – International Markets
The Regulatory Executive will be responsible for managing end-to-end regulatory activities for multiple global markets, ensuring timely product registrations and compliance with country-specific guidelines.
Key Responsibilities:
- Preparation and compilation of registration, re-registration, and variation dossiers as per country-specific regulatory guidelines
- Development of finished product dossiers in ACTD, CTD, and region-specific formats
- Handling dossiers for multiple dosage forms including tablets, capsules, injections (liquid, dry, PFS), eye drops, ear drops, suspensions, dry syrups, sachets, and oral liquids
- Detailed review of artworks for new registrations, re-registrations, and variations as per international regulatory requirements
- Coordination with marketing teams regarding dossier requirements, regulatory queries, and registration timelines
- Arrangement and dispatch of product samples with supporting regulatory documentation for various countries
- Review and coordination of product permissions, COPP, FSC, and interaction with local drug authorities
- Review of Drug Master Files (DMF) and coordination with API vendors to resolve regulatory queries
- Maintenance of regulatory documentation including registration trackers, aging analysis, and archival records
- Timely submission of GMP applications for multiple international markets
- Regulatory support for international tenders, particularly for African markets such as Ethiopia and Kenya
- Monthly regulatory planning meetings with management and internal regulatory teams
This role is well-suited for professionals targeting high-value regulatory affairs jobs with global exposure and long-term career progression.
Eligibility / Qualifications
- Bachelor’s degree in Pharmacy or Life Sciences (mandatory)
- 4 to 6 years of experience in pharmaceutical regulatory affairs
- Hands-on experience in international market registrations
- Preferred exposure to South East Asia, West Africa, LATAM, and CIS regions
- Strong understanding of ACTD, CTD, and country-specific regulatory requirements
- Proficiency in MS Word, Excel, and PowerPoint
- Excellent command of English, both written and verbal
Relevant Courses (Comma-Separated):
B.Pharmacy, M.Pharmacy, B.Sc Life Sciences, M.Sc Life Sciences, Pharmaceutical Sciences, Regulatory Affairs
Location & Salary
Work Location: Corporate Office / Manufacturing Unit (India)
Salary & Benefits:
Compensation will be offered as per industry standards and aligned with experience and regulatory expertise. Zenith Drugs provides attractive CTC packages along with statutory and performance-linked benefits.
Job Facilities Include:
- Provident Fund (PF)
- ESIC
- Gratuity
- Performance Bonus
- Travel Allowance / Daily Allowance (TA/DA)
Application Process
Interested candidates can apply directly by sharing their updated CV.
Email ID:
MHrsales@zenithdrugs.com
Contact Numbers:
+91 9179280571
+91 9770501859
Company Website:
https://www.zenithdrugs.com
Why Build Your Regulatory Career with Zenith Drugs
- Strong exposure to global pharmaceutical regulatory markets
- Hands-on experience with international product registrations
- Fast-track career growth to first-line managerial roles
- Incentive-based earnings and performance recognition
- Opportunities for international travel and market exposure
- Stable organization with expanding global footprint
Frequently Asked Questions (FAQs)
How many vacancies are available?
There are 2 openings for the Regulatory Executive position.
Is international regulatory experience mandatory?
Yes. Candidates must have hands-on experience with international regulatory submissions.
Which regions does this role primarily support?
South East Asia, West Africa, LATAM, CIS, and select African tender markets.
Is this role suitable for freshers?
No. A minimum of 4 years of regulatory experience is required.
Does the role include foreign travel?
Yes. The role offers opportunities for international travel based on regulatory and tender requirements.
Summary Table
| Category | Details |
|---|---|
| Company | Zenith Drugs Ltd |
| Vacancies | Regulatory Executive – International Markets (02) |
| Required Education | B.Pharm, M.Pharm, Life Sciences |
| Experience | 4–6 years in pharmaceutical regulatory affairs |
To apply for this job email your details to MHrsales@zenithdrugs.com
