Officer - Quality Control

Job Description:

Intas Pharmaceuticals is seeking a professional responsible for performing quality control analysis of in-process, finished product (FP), and process validation samples. The involves accurate testing, timely reporting, and adherence to regulatory and internal quality standards. The candidate will play a key in maintaining product quality,entifying deviations, and ensuring all observations are communicated promptly to the concerned authority.

Roles and Responsibilities:

• Perform analysis of in-process, finished product, and process validation samples as per assigned work and standard procedures
• Ensure accurate documentation of analytical results and preparation of reports along with raw data within defined timelines
• Submit test reports to the section in charge/designee with complete and compliant documentation
• Immediately report any abnormal observations, incidents, Out of Trend (OOT), and Out of Specification (OOS) results during analysis
• Follow all quality control procedures, SOPs, and regulatory guidelines during testing activities
• Maintain proper records, logs, and documentation for audit and compliance purposes
• Ensure cleanliness and proper upkeep of laboratory instruments and work areas
• Coordinate with team members and seniors to ensure smooth workflow and timely completion of analysis

Intas Pharmaceuticals Ltd. is a leading vertically integrated global pharmaceutical company engaged in formulation development, manufacturing, and marketing. The company is committed to addressing unmet medical and societal needs through a strong and comprehensive pharmaceutical value chain.

It operates globally through its subsidiaries under the brand
Accord Healthcare, enabling a strong presence in international markets.

Global Presence & Growth

• Present in 85+ countries worldwide
• Strong presence in North America, Europe, Latin America, Asia-Pacific, CIS & MENA regions
• Over 70% revenue from global markets
• Achieved ~19% CAGR growth
• Crossed $2.5 billion revenue milestone
• Ranked 6th in the Indian pharmaceutical market
• Among the top 10 generic players in regulated markets like the EU, US & UK

Infrastructure & Workforce

• 17 advanced facilities (manufacturing, R&D, distribution)
  • 10 in India
  • Others in the UK, Mexico & Greece
• Facilities approved by global regulators such as:
  • USFDA, EMA, MHRA, TGA, etc.
• Strong workforce of 23,000+ employees

Research & Development (R&D)

• Invests 6–7% of revenue in R&D
• 10,000+ product registrations worldwide
• Pipeline of 300+ high-value products including:
  • Biosimilars
  • New Drug Delivery Systems (NDDS)
  • First-to-File / First-to-Market products

Key Therapeutic Areas

• CNS (Central Nervous System)
• Cardiology
• Diabetology
• Gastroenterology
• Urology
• Oncology
• Animal Health

Specialized Capabilities

• Advanced Biopharma division focused on “Biosimilars for Billions”
• Expertise in niche therapies:
  • Oncology
  • Auto-immune diseases
  • Ophthalmology
  • Nephrology
  • Rheumatology
  • Hormone therapies
• Plasma Fractionation Unit for plasma-derived therapeutics with WHO-GMP certification

Quality & Compliance

• Manufacturing facilities approved by major global regulatory agencies
• Adherence to highest international quality standards
• Strong in-house development and quality control systems

Core Values

• Innovation – Driving continuous improvement
• Quality – Maintaining global standards
• Added Value – Delivering beyond expectations
• Growth – Continuous progress and expansion
• Commitment – Dedication to excellence
• Customer Delight & Collaboration
• Performance Focus & Care for Society

People & Culture

• Focus on attracting and retaining top talent
• Emphasis on diversity and global workforce
• Commitment to empowering employees and fostering growth