Associate Scientist - UPD

Job Description:

Intas Pharmaceuticals is seeking a professional to work in Upstream Process Development (UPD), focusing on the development and optimization of biologics manufacturing processes. The involves designing and executing experiments to improve cell culture performance, supporting scale-up activities, and ensuring smooth technology transfer to manufacturing. The candidate will collaborate closely with multiple functions to resolve process challenges and ensure robust and scalable upstream processes.

Roles and Responsibilities:

• Design and independently execute experiments for development and optimization of cell culture and fermentation processes, including batch, fed-batch, and perfusion systems
• Develop upstream processes for monoclonal antibodies (MAbs) and non-MAb biologics with minimal supervision
• Support technology transfer activities to ensure seamless transition from development to commercial manufacturing
• Collaborate with cross-functional teams including Cell Line Development, Downstream Processing, Quality, and Analytical teams to address process-related challenges
• Analyze data, interpret results, and recommend improvements or alternative approaches for process optimization
• Prepare technical reports, documentation, and presentations to communicate findings effectively
• Ensure adherence to quality, regulatory, and documentation standards within the laboratory environment

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