India's DMPLOI - Jobs & Networking AppIntas Pharmaceuticals Ltd., one of India’s leading pharmaceutical and biopharmaceutical organizations, has announced a Walk-In Drive at Thane for experienced professionals in the Upstream Processing (USP) and Downstream Processing (DSP) departments. This recruitment initiative offers an excellent opportunity for candidates looking to build their careers in the rapidly growing biosimilars manufacturing sector.
The company is expanding its biopharmaceutical capabilities and is seeking talented professionals with experience in microbial and cell culture operations. Selected candidates will work at Intas’ state-of-the-art Biopharma Plant in Ahmedabad, known for its advanced manufacturing technologies and global quality standards.
About Intas Biopharma
Intas Biopharma is recognized for its strong presence in the global pharmaceutical industry and its commitment to innovation, quality, and compliance. Employees gain exposure to:
Large-scale single-use bioreactor technologies
Global regulatory audits (FDA, EMA, and ROW markets)
Advanced data analytics platforms such as JMP and SIMCA
End-to-end USP and DSP manufacturing operations
A collaborative and employee-friendly work culture
Open Positions
Upstream Processing (USP) – Microbial & Cell Culture
Designation: Executive / Sr. Executive / Assistant Manager
Educational Qualification:
M.Sc.
B.Tech
M.Tech in Bioprocess, Biotechnology, Microbiology, or Biochemistry
Experience Required: 1–10 Years
Key Skills:
Biosimilar manufacturing processes
Large-scale bioreactor operations
Single-use systems and perfusion technologies
Continuous and batch centrifugation
High-pressure homogenization
Aseptic processing techniques
GMP compliance and data analysis
Downstream Processing (DSP) – Microbial & Cell Culture
Designation: Executive / Sr. Executive
Educational Qualification:
M.Sc.
B.Tech
M.Tech in Bioprocess, Biotechnology, Microbiology, or Biochemistry
Experience Required: 1–10 Years
Key Skills:
Chromatography operations
AKTA platform handling
Column packing and qualification
TFF (Tangential Flow Filtration)
Nanofiltration and aseptic filtration
Buffer preparation
GMP knowledge and compliance
Walk-In Interview Details
Date: 28th June 2026 (Sunday)
Time: 09:30 AM to 05:00 PM
Venue:
Ibis Hotel Thane
Plot No. 02, Pokharan Road No. 1
Tulsi Dham, Samata Nagar
Thane West, Mumbai, Maharashtra – 400606
Job Location: Ahmedabad Biopharma Plant
Why Professionals Should Consider This Opportunity
The biopharmaceutical industry is experiencing significant growth globally, creating strong demand for skilled USP and DSP professionals. Intas offers exposure to advanced manufacturing technologies, international regulatory standards, and large-scale biosimilar production facilities. Candidates with relevant experience can benefit from professional growth, technical learning, and opportunities to work on cutting-edge bioprocess technologies.
Technical FAQs
1. What is the difference between Upstream Processing (USP) and Downstream Processing (DSP)?
USP focuses on cultivating cells or microorganisms to produce the desired biological product, while DSP involves purification, filtration, and recovery of the product to achieve the required quality and purity standards.
2. Why are single-use bioreactors widely used in biosimilar manufacturing?
Single-use bioreactors reduce contamination risks, minimize cleaning validation requirements, improve operational flexibility, and shorten production turnaround times compared to traditional stainless-steel systems.
3. What is the role of Tangential Flow Filtration (TFF) in DSP?
TFF is used for concentration, diafiltration, and buffer exchange of biological products. It helps maintain product integrity while efficiently removing impurities and unwanted components.
4. How does chromatography contribute to biopharmaceutical purification?
Chromatography separates target proteins from impurities based on properties such as charge, size, or affinity, helping achieve high product purity and regulatory compliance.
5. Why is GMP compliance critical in biopharmaceutical manufacturing?
Good Manufacturing Practices (GMP) ensure product quality, safety, consistency, and traceability. Regulatory agencies such as the FDA and EMA require strict GMP adherence for product approval and market distribution.
Disclaimer: Intas Pharmaceuticals does not charge any fee for recruitment, application processing, training, or employment opportunities. Candidates should be cautious of fraudulent job offers and recruitment scams.
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