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Hiring: Cadila Pharmaceuticals (QA Validation, Analytical R&D & Regulatory Affairs)


Hiring: Cadila Pharmaceuticals (QA Validation, Analytical R&D & Regulatory Affairs)

For pharmaceutical professionals and researchers looking for non-walk-in, direct email applications, Cadila Pharmaceuticals Limited—one of India's premier healthcare and API/formulation companies—is accepting direct resume submissions for multiple specialized technical openings.

Below is a structured overview of these direct positions for your blog:

📌 Role & Location Overview

  • Company: Cadila Pharmaceuticals Limited
  • Locations: Dholka (Ahmedabad) & Bhat (Gandhinagar), Gujarat
  • Departments: Quality Assurance (Validation), Analytical R&D (API), and Regulatory Affairs (RA)
  • Experience Required: 2 to 9 Years
  • Application Mode: Direct Email CV Submission

🎯 Technical Positions & Requirements

1. QA Executive – Process & Equipment Validation

  • Location: Dholka Plant, Ahmedabad
  • Qualifications: B.Pharm / M.Pharm / M.Sc
  • Experience Required: 3 to 7 Years
  • Core Responsibilities: Preparing and executing Process Validation, Cleaning Validation, and Equipment Qualification protocols for oral solid dosage (OSD) and injectable lines.

2. Research Scientist – Analytical R&D (API)

  • Location: R&D Center, Bhat, Gandhinagar
  • Qualifications: M.Sc (Analytical / Organic Chemistry) / M.Pharm
  • Experience Required: 4 to 9 Years
  • Core Responsibilities: Method development and validation for active pharmaceutical ingredients (APIs) using HPLC, GC-MS, LC-MS, and handling structure elucidation.

3. Officer / Executive – Regulatory Affairs (DRA)

  • Location: Corporate Campus, Bhat
  • Qualifications: B.Pharm / M.Pharm
  • Experience Required: 2 to 5 Years
  • Core Responsibilities: Dossier preparation (eCTD format), filing regulatory submissions for semi-regulated and regulated markets, and managing query responses.

📋 Resume Submission Guidelines

When submitting your application via email, ensure your CV includes:

  • Explicit details of regulatory guidelines handled (e.g., USFDA, EU-GMP, WHO).
  • Current company details, designations held, and notice period.
  • Updated contact details and key technical tools/instruments used.

📬 How to Apply (Direct Email Application)

Eligible candidates can email their updated CV directly to the Cadila HR talent acquisition team:

📧 Email CV to: talent.acquisition@cadilapharma.co.in (Subject Line Format: "Application for [Position Title] - [Department] - [Years of Experience]")

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