Intas Pharmaceuticals Limited – Walk-In Interview for QA, Packing – OSD in Ahmedabad on 24th May

Are you ready to advance your career with a global leader in pharmaceuticals? Intas Pharmaceuticals Limited, one of the world’s leading multinational companies in formulation development, manufacturing, and marketing, is hosting a walk-in interview drive on May 24, 2025, in Ahmedabad, Gujarat.

With a presence in over 85 countries and a 20% CAGR, Intas is renowned for its commitment to quality, innovation, and regulatory compliance with standards like USFDA and MHRA. Join us at our state-of-the-art facility in Pharmez, Ahmedabad, and contribute to creating a world of good health, happiness, and hope!

About Intas Pharmaceuticals Limited

Intas Pharmaceuticals Limited, headquartered in Ahmedabad, India, is a global powerhouse in pharmaceutical formulation development, manufacturing, and marketing. With over three decades of expertise, Intas operates in more than 85 countries, with 70% of its revenue from highly regulated markets like the EU and US.

Our 14 manufacturing facilities, including 7 in India, are accredited by USFDA, EMA, MHRA, and TGA. Intas is a leader in chronic therapies like oncology, neurology, and cardiology, and is the first Indian company with a biologics manufacturing facility accredited by the European Health Authority.

Join our team to work in a dynamic, innovation-driven environment focused on improving global health.

We are hiring for multiple roles in Quality Assurance (QA) and Oral Solid Dosage (OSD) Packing at our Pharmez facility in Ahmedabad. Candidates with experience in regulated plants (USFDA, MHRA, EU) are encouraged to attend our walk-in interview on May 24, 2025.

Walk-In Interview Details

• Date: Saturday, May 24, 2025
• Time: 9:00 AM to 3:00 PM
• Venue: Intas Pharmaceuticals Ltd, Plot No. 5 to 14, Pharmez, Near Village Matoda, Sarkhej-Bavla National Highway No. 8-A, Taluka Sanand, Dist. Ahmedabad-382213, Gujarat
• Job Location: Intas Pharmez, Ahmedabad
• Contact: Email your resume to hr_matoda@intaspharma.com if unable to attend

What to Bring:

• Updated resume
• Original and photocopies of final year mark sheets/degree certificate
• CTC breakup and recent salary slips
• Educational and experience certificates

Important Notes:

• Candidates must have experience in regulated plants (e.g., USFDA, MHRA, EU)
• Candidates interviewed at Intas in the last 6 months are not eligible
• Willingness to work in shift duties is required
• Intas does not charge any fees for job applications, processing, training, or testing
• Formulation pharma experience in regulated plants is mandatory

Available Positions

Below is a user-friendly breakdown of the open roles, qualifications, experience requirements, and responsibilities. All positions require experience in pharmaceutical formulation, preferably in regulated environments like USFDA or MHRA.

1. Quality Assurance – Stability & Retain Sample (Officer/Sr. Officer/Executive/Sr. Executive)

• Experience: 2-10 years
• Qualification: M.Sc., B.Pharm, M.Pharm

Key Skills:

• Expertise in stability chamber management and retain sample reviews
• Experience in charging and withdrawing stability samples as per schedule
• Monitoring and managing walk-in stability chambers
• Stability data submission to regulatory authorities
• Knowledge of GMP and QMS

What You’ll Do:

• Manage stability chamber operations and retain sample processes
• Charge finished product stability samples and withdraw as per schedule
• Submit stability data to regulatory affairs
• Ensure compliance with regulatory and corporate standards

2. Quality Assurance – Documentation Cell (Officer)

• Experience: 2-10 years
• Qualification: M.Sc., B.Pharm, M.Pharm

Key Skills:

• Proficiency in QA documentation, including SOPs, BMRs, and BPRs
• Experience in document receipt, review, and archival in software systems
• Knowledge of document reconciliation and GMP compliance

What You’ll Do:

• Receive, review, and issue QA documents as per requirements
• Reconcile and archive completed documents
• Review and approve SOPs to ensure compliance
• Support documentation for regulatory audits

3. OSD Packing – Primary Packing (Officer/Executive)

• Experience: 2-8 years
• Qualification: B.Pharm

Key Skills:

• Expertise in operating primary packing machines (blister, strip, bottle packing)
• Proficiency in performing in-process checks (weight variation, visual inspection, seal integrity)
• Knowledge of GMP and packing line operations

What You’ll Do:

• Operate and monitor primary packing machines
• Conduct in-process checks for quality assurance
• Ensure compliance with GMP and regulatory standards
• Maintain accurate packing records

4. OSD Packing – Vendor Management & Artwork (Sr. Executive/Assistant Manager/Manager)

• Experience: 2-16 years
• Qualification: B.Pharm, M.Pharm, M.Sc.

Key Skills:

• Expertise in vendor management for APIs, excipients, and packaging materials
• Proficiency in SAP and QMS software for documentation
• Experience in preparing and reviewing software qualification documents
• Conducting vendor audits for contract labs and suppliers

What You’ll Do:

• Manage vendor documentation and audits for raw materials and packaging
• Handle SAP and QMS software for vendor management
• Prepare and review artwork and qualification documents
• Ensure compliance with regulatory standards

5. Corporate Quality Assurance (CQA) – Documentation Team (Officer/Sr. Executive)

• Experience: 2-16 years
• Qualification: B.Pharm, M.Pharm, M.Sc.

Key Skills:

• Expertise in reviewing and approving site SOPs, master documents (e.g., MPCR, BPCR)
• Knowledge of corporate documentation and centralized record systems
• Familiarity with regulatory and corporate standards

What You’ll Do:

• Review and approve site SOPs and master documents
• Maintain centralized corporate documentation systems
• Ensure compliance with regulatory and corporate standards
• Support audits and documentation processes

6. Corporate Quality Assurance (CQA) – Loan License/Third Party (Executive/Sr. Executive/Assistant Manager/Manager)

• Experience: 2-16 years
• Qualification: B.Pharm, M.Pharm, M.Sc.

Key Skills:

• Expertise in vendor and third-party management
• Experience in conducting qualification audits for raw materials, packaging, and contract manufacturers
• Knowledge of maintaining approved vendor lists and monitoring compliance

What You’ll Do:

• Perform vendor qualification audits for raw materials and contract manufacturers
• Maintain and monitor approved vendor lists
• Ensure third-party compliance with regulatory standards
• Coordinate with vendors to support manufacturing operations

7. Quality Assurance – Regulatory (Senior Executive)

• Experience: 2-10 years
• Qualification: M.Sc., B.Pharm, M.Pharm

Key Skills:

• Expertise in submitting quality documents to regulatory affairs
• Knowledge of end-to-end regulatory compliance processes
• Proficiency in data entry for regulatory submissions and QMS (OOS, OOT, Deviations)
• Familiarity with GMP and regulatory audits

What You’ll Do:

• Submit quality documents to regulatory affairs
• Review and implement regulatory compliance activities
• Perform data entries for regulatory submissions
• Ensure GMP compliance in daily operations

8. Corporate Quality Assurance (CQA) – Compliance & Documentation Cell (Manager/Sr. Executive)

• Experience: 2-16 years
• Qualification: B.Pharm, M.Pharm, M.Sc.

Key Skills:

• Expertise in conducting internal audits across manufacturing units
• Proficiency in reviewing and approving SOPs, MPCR, and other master documents
• Knowledge of corporate documentation and centralized record systems
• Familiarity with GMP and regulatory compliance

What You’ll Do:

• Conduct and coordinate internal audits for manufacturing units
• Review and approve site SOPs and master documents
• Maintain centralized corporate documentation systems
• Ensure compliance with regulatory and corporate standards

Why Join Intas Pharmaceuticals Limited?

• Global Leadership:
  • Work with a top-tier pharmaceutical company present in over 85 countries
  • Contribute to high-quality formulations for chronic and acute therapies
• Career Growth:
  • Access opportunities to work with cutting-edge technologies and biologics
  • Grow in a company with a 20% CAGR and global expansion
• Innovation-Driven:
  • Be part of a team with 13 commercialized biosimilars and 15 in development
  • Support regulatory approvals from USFDA, MHRA, and EMA
• Supportive Culture:
  • Join a purpose-driven workplace focused on health, happiness, and hope
  • Work in a facility with a 3.8/5 employee rating for work culture

How to Apply

• Email your CV to hr_matoda@intaspharma.com
• Include details of your formulation experience in regulated plants, current salary, and notice period

Note:

• Candidates with experience in USFDA, MHRA, or EU-regulated plants are preferred
• Those interviewed in the last 6 months are not eligible
• Intas does not charge any fees for job applications or processes

For more information about Intas Pharmaceuticals Limited, visit our website.

Frequently Asked Questions (FAQs)

Join Intas Pharmaceuticals Limited in Ahmedabad and be part of a globally recognized leader in pharmaceutical innovation. Attend our walk-in interview on May 24, 2025, or apply online to take the next step in your career!