jobaspirants.online

Pharma, Life Science, Health Care, Engineering Job, Govt Job Updates
Menu
  • Home
  • Pharma Jobs
  • Govt Jobs
  • ENGG Jobs
  • WFH Jobs

Freshers & Experience Jobs Group Join WhatsApp

Join Now
Home
Pharma Jobs
Intas Pharmaceuticals Walk-In Interview in Ahmedabad on 11 January 2026 – QA, QC & Production Jobs

Intas Pharmaceuticals Walk-In Interview in Ahmedabad on 11 January 2026 – QA, QC & Production Jobs

chandrakanth February 26, 2026
close

Discover exciting pharma jobs in Ahmedabad with Intas Pharmaceuticals‘ walk-in interview on 11 January 2026. Multiple openings in QA jobs, QC jobs, production jobs, and injectable/OSD manufacturing roles await qualified candidates.

About the Company

Intas Pharmaceuticals Ltd. is a leading multinational pharmaceutical company headquartered in India, with a strong global footprint in over 85 countries. Known for its rapid growth at approximately 20% CAGR, Intas derives around 70% of its revenue from highly regulated international markets, including the EU and US.

The company excels in formulation development, manufacturing, and marketing, with a commitment to quality, innovation, and regulatory compliance. Recognized as a Great Place To Work®, Intas fosters an environment of health, happiness, and hope for its employees and communities worldwide.

Job Details

  • Company Name: Intas Pharmaceuticals Ltd.
  • Experience: 3–11 years (varies by role)
  • Qualification: ITI/Diploma, B.Pharm/M.Pharm, M.Sc.
  • Location: Ahmedabad, Gujarat
  • Work Type: On-site (shift duties applicable for several roles)

Job Description

Intas Pharmaceuticals is hiring experienced professionals for its state-of-the-art facilities in Ahmedabad, including injectable and oral solid dosage (OSD) manufacturing units.

The openings span production, quality assurance, and quality control functions in highly regulated plants approved by USFDA, MHRA, and EU authorities. Candidates with formulation experience in regulated environments are strongly preferred.

Technician/Operator – Injectable Manufacturing

  • Department: Injectable Manufacturing
  • Experience: 3–10 years
  • Qualification: ITI/Diploma

Senior Executive/Executive – IPQA-Sterile

  • Department: In-Process Quality Assurance (Sterile)
  • Experience: 6–11 years
  • Qualification: B.Pharm/M.Pharm

Senior Executive/Executive – Quality Assurance (Doc Cell)

  • Department: Quality Assurance – Documentation Cell (Shift duties)
  • Experience: 6–11 years
  • Qualification: B.Pharm/M.Pharm

Senior Executive/Executive – 21 CFR Compliance

  • Department: 21 CFR (Part 11 & EU Annex 11) – Self Inspection, Audit Trail, Electronic Data Management
  • Experience: 6–11 years
  • Qualification: B.Pharm/M.Pharm

Senior Officer/Officer – Quality Control (Environment Monitoring)

  • Department: Quality Control – Environment Monitoring (Shift duties)
  • Experience: 3–6 years
  • Qualification: B.Pharm/M.Pharm

Technician/Operator – OSD Packing

  • Department: OSD Packing
  • Experience: 3–10 years
  • Qualification: ITI/Diploma

Senior Executive/Executive – Quality Assurance (Qualification)

  • Department: Quality Assurance – Qualification (Shift duties)
  • Experience: 6–11 years
  • Qualification: B.Pharm/M.Pharm

Senior Executive/Executive – CQA Audit Compliance

  • Department: Corporate Quality Assurance – Audit Compliance (OSD/Micro Site Audits)
  • Experience: 6–11 years
  • Qualification: B.Pharm/M.Pharm/M.Sc.

Senior Executive/Executive – Quality Control (Finished Products & AMV)

  • Department: Quality Control – Finished Products & Analytical Method Validation (Shift duties)
  • Experience: 6–11 years
  • Qualification: B.Pharm/M.Pharm

Skills/Qualifications

  • Proven experience in USFDA/MHRA/EU-regulated pharmaceutical plants
  • Hands-on formulation exposure in injectable or OSD manufacturing
  • Strong knowledge of cGMP, 21 CFR Part 11, and EU Annex 11 (for relevant roles)
  • Willingness to work in rotational shifts
  • Excellent documentation and compliance skills
  • Analytical mindset with attention to detail

Key Responsibilities

  • Execute manufacturing/packing operations as per SOPs
  • Perform in-process quality checks and documentation
  • Conduct environmental monitoring and microbial testing
  • Manage qualification, validation, and audit compliance activities
  • Review electronic data and audit trails
  • Ensure adherence to regulatory standards

Benefits/Perks

  • Rapid career growth in a 20% CAGR organization
  • Exposure to global regulated markets
  • Great Place To Work® certified culture
  • Continuous learning and skill development opportunities
  • Competitive compensation package
  • Stable long-term employment in a leading pharma company

How to Apply

Interested candidates should attend the walk-in interview with an updated resume, original and photocopies of educational certificates, experience letters, recent salary slips, and CTC breakdown. Candidates who have appeared for an interview at Intas in the last six months are not eligible.

Intas Pharmaceuticals does not charge any fee at any stage of recruitment. Beware of fraudulent offers.

Verified Post

Verification: To confirm the legitimacy of this posting, you can view the original announcement on the Intas Pharma LinkedIn page.

Intas Pharmaceuticals Walk-In Interview in Ahmedabad on 11 January 2026 – QA, QC & Production Jobs

For more pharma job opportunities across India, visit Pharma Recruiter.

Take the next step in your pharmaceutical career – attend the walk-in and join a world-class organization!

Walk-in Interview Details

  • Date: 11 January 2026 (Sunday)
  • Time: 09:30 AM to 04:30 PM
  • Venue: Pride Plaza Hotel Ahmedabad, Judges Bungalow Road, off Sarkhej-Gandhinagar Highway, Bodakdev, Ahmedabad, Gujarat 380054

Why You Should Join

Intas Pharmaceuticals offers more than just a job—it provides a platform for meaningful career growth in a globally respected organization. As a Great Place To Work® certified company, Intas promotes a supportive, innovative, and inclusive culture where employees contribute to improving global health.

With strong presence in regulated markets and consistent double-digit growth, Intas ensures long-term stability, continuous learning, and opportunities to work on cutting-edge pharmaceutical technologies.

FAQs

Who is eligible to apply?

Candidates with 3–11 years of relevant experience in regulated (USFDA/MHRA/EU) formulation plants and the required qualifications. Those interviewed at Intas in the last six months are not eligible.

Is there any application fee?

No. Intas Pharmaceuticals does not charge any fee for job applications, processing, training, or testing.

What documents should I carry?

Updated resume, original and photocopies of final year mark sheets, degree certificates, experience letters, salary slips, and CTC breakdown.

Are shift duties mandatory?

Yes, several roles involve rotational shift duties. Only candidates open to shifts should apply.

Post Views: 1

Related posts:

  1. Unilever Jobs for Freshers | Associate Global Market Vigilance (Pharmacovigilance)
  2. Sun Pharmaceutical Industries Hiring 2026 | Executive – Analytical Development R&D Jobs – Baroda
  3. “Intas Pharmaceuticals Walk In Drive 2025 | Jobs in Multiple Departments”
  4. “Lubrizol Careers 2025 | Hiring Production Executive – Navi Mumbai Maharashtra”
Share
Pinterest
Tweet
Email
Linkedin
Whatsapp
Telegram
Prev Article
Next Article

Leave a Reply Cancel Reply

Enter your Email Address

Subscribe to our mailing list and get interesting stuff and updates to your email inbox.

Thank you for subscribing.

Something went wrong.

Deliveried By JobAspirants.Online

Latest Walk-Ins

  • Group Lead Formulation Development Job Openings at Aizant | OSD | Hyderabad
  • MSN Laboratories is Hiring for Quality Assurance Roles
  • Regulatory Affairs Officer API Job in Mumbai
  • Research Associate Clinical Research at Unichem
  • Clinical Research Associate Job at Apotex

jobaspirants.online

Pharma, Life Science, Health Care, Engineering Job, Govt Job Updates
Copyright © 2026 jobaspirants.online