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Intas Pharmaceuticals is Hiring for QA, QC, and Production Roles on 21st December

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Discover top pharma jobs at Intas Pharmaceuticals‘ walk-in interview in Hyderabad. Explore QA jobs, QC jobs, production jobs, and pharmaceutical careers in India with global growth opportunities.

About the Company

Intas Pharmaceuticals Ltd. stands as a global leader in pharmaceutical formulation development, manufacturing, and marketing. With operations spanning over 85 countries and a robust 20% CAGR, the company derives 70% of its revenues from highly regulated markets like the EU and US.

Certified as a Great Place to Work, Intas prioritizes innovation, regulatory compliance, and employee well-being to foster a world of good health, happiness, and hope.

Job Details

  • Company Name: Intas Pharmaceuticals Ltd.
  • Experience: Varies by role (1 to 12 years)
  • Qualification: B.Pharm, M.Pharm, B.Sc, M.Sc (in Microbiology, Organic Chemistry, Analytical Chemistry), BE/B.Tech, Diploma in relevant fields
  • Location: Ahmedabad

Job Description

Intas Pharmaceuticals is hosting a walk-in drive to recruit talented professionals across engineering, research, quality, and manufacturing departments.

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These pharma jobs emphasize hands-on expertise in regulated environments, supporting the company’s mission in injectable, OSD, and parenteral formulations. Multiple positions are available for experienced candidates seeking pharmaceutical careers in India.

Senior Executive/Executive/Senior Officer

  • Department: Engineering (Instrumentation/QMS/Plant Maintenance/Qualification/21 CFR)
  • Experience: 3 to 10 years
  • Education/Qualification: BE/B.Tech

Research Associate/Sr. Research Associate

  • Department: Process Development/MS&T – OSD/Parenteral
  • Experience: 2 to 6 years
  • Education/Qualification: M.Pharm

Officer/Senior Officer/Executive

  • Department: Microbiology
  • Experience: 2 to 7 years
  • Education/Qualification: B.Sc/M.Sc (Microbiology)

Executive/Senior Officer/Officer/Associate/Senior Associate

  • Department: Injectable – Manufacturing & Packing & Visual Inspection & QMS
  • Experience: 1 to 5 years
  • Education/Qualification: B.Pharm/M.Pharm/M.Sc/B.Sc/Diploma

Research Associate/Sr. Research Associate

  • Department: Analytical Development – Formulation
  • Experience: 3 to 8 years
  • Education/Qualification: B.Pharm/M.Pharm/M.Sc

Officer/Senior Officer/Executive/Senior Executive

  • Department: Quality Assurance – IPQA (OSD) & QMS/Documentation/Qualification and Validation
  • Experience: 2 to 9 years
  • Education/Qualification: B.Pharm/M.Pharm/M.Sc

Research Associate/Sr. Research Associate/Research Scientist

  • Department: Formulation Development – Injectable/OSD
  • Experience: 4 to 12 years
  • Education/Qualification: M.Pharm

Officer/Senior Officer/Executive

  • Department: Quality Control
  • Experience: 4 to 12 years
  • Education/Qualification: B.Sc/M.Sc (Organic Chemistry/Analytical Chemistry), B.Pharm/M.Pharm

Skills/Qualifications

  • Thorough knowledge of cGMP norms and laboratory safety protocols
  • Relevant functional experience in regulatory-approved facilities
  • Strong technical proficiency in instrumentation, microbiology, or formulation development
  • Proficiency in quality management systems (QMS) and validation processes
  • Excellent documentation and compliance skills for EU/US markets
  • Bachelor’s or Master’s degree in pharmacy, science, or engineering fields

Key Responsibilities

  • Conduct equipment qualification and maintenance tasks
  • Perform analytical testing and process development
  • Ensure microbial quality control in production lines
  • Execute visual inspections and packing operations
  • Validate formulations for injectables and OSD
  • Document QMS activities and regulatory audits
  • Support IPQA reviews for compliance

Benefits/Perks

  • Robust career growth in a 20% CAGR global pharma leader
  • Continuous learning through innovation-driven projects
  • Competitive salary and performance incentives
  • Collaborative work culture certified by Great Place to Work
  • Global exposure to EU and US regulated markets
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How to Apply

To apply for these pharma jobs, attend the walk-in interview with your updated resume, educational certificates, experience letters, and salary documents. Candidates who have interviewed with Intas in the last six months should not apply.

Verified Post

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

Walk-In Interview for Pharma Jobs at Intas Pharmaceuticals: QA, QC, and Production Roles in India

For more pharmaceutical careers in India, visit Pharma Recruiter. Intas does not charge any fees for applications—beware of scams. Secure your future today: Walk in and showcase your potential for exciting prospects!

Walk-in Interview Details

  • Date: 21 December 2025 (Sunday)
  • Time: 09:30 am to 05:00 pm
  • Venue: Radisson – Hyderabad Hitech City, Gachibowli, Miyapur Road, Hyderabad, Telangana – 500032, India

Why You Should Join

Intas Pharmaceuticals offers a vibrant company culture recognized as a Great Place to Work, where innovation meets regulatory excellence. Employees enjoy long-term career stability amid rapid global expansion, with ample learning opportunities in cutting-edge formulation and quality roles.

Join a compliance-focused environment that drives pharmaceutical careers in India toward impactful, hope-filled contributions to healthcare worldwide.

FAQs

Who is eligible for these QA jobs and QC jobs at Intas?

Candidates with 1-12 years of experience in pharma roles, holding B.Pharm, M.Pharm, B.Sc/M.Sc, or BE/B.Tech degrees, and knowledge of cGMP norms qualify. Prior experience in regulated facilities is preferred.

What is the application process for this walk-in interview?

Simply attend the event on 21 December 2025 with your resume and documents. No online submission required—direct interviews for shortlisting.

What growth opportunities exist in pharmaceutical careers at Intas?

Expect rapid advancement in global markets, skill-building in EU/US compliance, and exposure to 20% CAGR growth, fostering long-term stability and innovation.

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