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Aculife Healthcare Hiring Regulatory Affairs Trainee

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Aculife Healthcare Pvt. Ltd. (Nirma Group) has announced an exciting opportunity for M.Pharm graduates seeking a career in Regulatory Affairs (RA). The company is hiring for the role of Trainee Officer – Regulatory Affairs at its Ahmedabad head office.

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This is an excellent opportunity for freshers and early professionals with 6 months to 1 year of Regulatory Affairs experience, including internships or apprenticeships, to enter the pharmaceutical regulatory domain and work on global markets like LATAM and EU.


Job Overview

  • Position: Trainee Officer – Regulatory Affairs
  • Location: Ahmedabad, Gujarat
  • Experience: 6 months to 1 year (RA internship/apprenticeship accepted)
  • Qualification: M.Pharm (Regulatory Affairs / Pharmaceutics preferred)
  • Industry: Pharmaceutical / Healthcare

Key Responsibilities

The selected candidate will be involved in core Regulatory Affairs operations, including:

  • Compilation and review of registration dossiers as per country-specific guidelines
  • Handling submissions for LATAM markets (Brazil, Mexico) and exposure to EU regulatory requirements
  • Reviewing critical technical documents such as:
    • Drug Master File (DMF)
    • Product Development Report
    • Batch Manufacturing Record (BMR) & Batch Packaging Record (BPR)
    • Analytical Method Validation Reports
    • Stability Reports & BE Study Reports
  • Preparing deficiency responses and managing backlog dossiers
  • Supporting post-approval changes (variations) as per regulatory guidelines
  • Coordination with global regulatory teams, agents, and distributors
  • Reviewing artworks and packaging materials for product launches
  • Maintaining and updating regulatory databases and submission records

Eligibility Criteria

To apply for this Regulatory Affairs job in Ahmedabad, candidates must meet the following criteria:

  • M.Pharm degree (mandatory)
  • 6–12 months experience in Regulatory Affairs (including internships)
  • Basic knowledge of CTD/eCTD, DMF, and dossier compilation
  • Understanding of global regulatory guidelines (EU, LATAM preferred)
  • Strong attention to detail and documentation skills

Salary & Benefits

  • Salary Range: ₹2.5 LPA – ₹4.5 LPA (Expected for trainee-level roles)
  • Opportunity to work with a leading pharma company under Nirma Group
  • Hands-on experience in international regulatory submissions
  • Career growth in Regulatory Affairs domain

Why This Job is Important for Pharma Freshers

This role is highly relevant for candidates targeting careers in:

  • Regulatory Affairs (RA)
  • Pharmaceutical Documentation
  • Global Submissions (EU, LATAM markets)
  • Dossier Preparation & Lifecycle Management

With increasing demand for Regulatory Affairs professionals in India, this opportunity provides strong exposure to international compliance standards, making it ideal for long-term career growth.


How to Apply

Interested and eligible candidates can apply by sending their updated resume to:

📧 satabdeerath@aculife.co.in

Tip: Mention “Application for RA Trainee Officer – Ahmedabad” in the subject line to improve visibility.

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