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Zenotech Laboratories is Hiring for Regulatory Affairs Executive

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Zenotech Laboratories

B.Pharm or M.Pharm qualification is mandatory

Hyderabad

4–8 years

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Zenotech Laboratories Limited is inviting applications for the position of Regulatory Affairs / Liaisoning – Sr. Executive / Manager at its Hyderabad location. This is an excellent opportunity for experienced pharma professionals who want to build a strong career in regulatory affairs across formulation and biologics segments.

The company is looking for candidates who can handle regulatory submissions, coordinate with authorities, and ensure compliance with evolving regulatory requirements in India.


Job Overview

Company: Zenotech Laboratories Limited
Location: Hyderabad, India
Role: Sr. Executive / Manager – Regulatory Affairs
Department: Regulatory Affairs / Liaisoning
Unit: Formulation (Orals / Non-Orals / Biologics)
Experience: 4 – 8 Years
Qualification: B.Pharm / M.Pharm
Employment Type: Full-Time, Permanent


Job Description

The selected candidate will be responsible for preparing, reviewing, and submitting high-quality regulatory dossiers for Oral Solid Dosage (OSD), Non-Oral dosage forms, and Biologics for the Indian market. The role requires strong knowledge of regulatory systems, documentation, and coordination with authorities to ensure smooth approvals.


Key Responsibilities

  • Handle various regulatory application submissions through online portals
  • Work extensively on ODLS (Telangana) and ONDLS portals
  • Prepare, review, and manage regulatory dossiers and documentation
  • Track application status and coordinate with regulatory authorities
  • Manage approvals, inspections, and compliance timelines
  • Maintain regulatory databases, records, and licenses
  • Coordinate with cross-functional teams for submission readiness
  • Ensure compliance with updated regulatory guidelines and changes

Required Qualifications & Skills

  • B.Pharm or M.Pharm qualification is mandatory
  • 4 to 8 years of experience in Regulatory Affairs
  • Strong knowledge of Indian regulatory requirements
  • Hands-on experience with ODLS and ONDLS portals
  • Good documentation and dossier preparation skills
  • Strong communication and coordination abilities

Salary & Benefits

  • Estimated Salary: ₹6 LPA – ₹12 LPA (depending on experience and role level)
  • Opportunity to work with a reputed pharmaceutical organization
  • Exposure to regulatory processes across multiple dosage forms
  • Career growth in regulatory and compliance domain
  • Professional work environment and learning opportunities

How to Apply

Interested candidates can apply using the following methods:

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