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Intas Pharmaceuticals Hiring For Injectable Manufacturing, Quality Control, Quality Assurance, Engineering, Microbiology

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Intas Pharmaceuticals Ltd. is conducting a Walk-In Interview Drive in Sanand (Ahmedabad) for multiple departments including Injectable Manufacturing, Quality Control (QC), Quality Assurance (QA), Engineering, and Microbiology.

With presence in 85+ countries and strong growth in regulated markets like the US & EU, Intas offers excellent career growth for pharma professionals.


📌 Walk-In Interview Details

  • 📅 Date: 19 April 2026 (Sunday)
  • ⏰ Time: 09:30 AM – 03:00 PM
  • 📍 Location: Sanand, Ahmedabad
  • 🏢 Venue:
    Intas Pharmaceuticals Ltd.
    Plot No. 85-87, Kailash Industrial Estate,
    Sanand-Viramgam Highway, Village Iyava,
    Ahmedabad – 382110

💼 Job Openings & Departments

1️⃣ Injectable Manufacturing & Packing

  • Roles: Executive / Sr. Officer / Officer / Jr. Officer / Associate / FTE
  • Qualification: B.Pharm / M.Pharm / B.Sc / M.Sc / Diploma / ITI
  • Experience: 1–8 Years

2️⃣ Quality Control (QC)

  • Roles: Officer / Sr. Officer / Executive
  • Qualification: B.Sc / M.Sc (Organic/Analytical Chemistry), B.Pharm / M.Pharm
  • Experience: 2–6 Years

3️⃣ Engineering (Maintenance & Utility)

  • Roles: Officer / Sr. Officer / Executive
  • Qualification: BE / B.Tech / Diploma (Mechanical / Electrical)
  • Experience: 3–8 Years

4️⃣ Quality Assurance (QA – IPQA/QMS)

  • Roles: Officer / Sr. Officer / Executive
  • Qualification: B.Pharm / M.Pharm / M.Sc
  • Experience: 2–6 Years

5️⃣ Microbiology

  • Roles: Officer / Sr. Officer / Executive
  • Qualification: B.Sc / M.Sc (Microbiology)
  • Experience: 2–7 Years

🧾 Key Responsibilities

  • Ensure compliance with cGMP guidelines and regulatory standards
  • Perform quality control testing (HPLC, analysis, documentation)
  • Execute IPQA and QMS activities
  • Handle injectable manufacturing & packing operations
  • Manage engineering maintenance, utilities, and equipment validation
  • Conduct microbiological testing and environmental monitoring
  • Maintain proper documentation and audit readiness

🎓 Qualifications & Skills

  • Pharma/Science background: B.Pharm, M.Pharm, B.Sc, M.Sc, BE/B.Tech
  • Strong understanding of cGMP, GLP, and regulatory compliance
  • Experience in USFDA/EU-approved facilities preferred
  • Knowledge of laboratory safety and documentation practices
  • Good communication and teamwork skills

🎁 Benefits of Joining Intas

  • Opportunity to work with a global pharmaceutical leader
  • Exposure to regulated markets (US/EU)
  • Competitive salary and growth opportunities
  • Professional development in advanced pharma manufacturing
  • Stable and long-term career prospects

📄 Documents to Carry

  • Updated Resume (CV)
  • Educational Certificates
  • Experience Letters
  • Salary Slips & CTC Details
  • Aadhar Card & PAN Card

⚠️ Important Note:
Candidates who attended an interview at Intas in the last 6 months are not eligible.

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