Aragen Lifesciences Walk-In Manufacturing, Process Development, QC, QA

Join Aragen Lifesciences: Biologics Manufacturing, QC, QA, and Development Roles in Bengaluru & Hyderabad

Apply now for Executive to Manager-level positions in biologics at Aragen Lifesciences in Bengaluru. Openings in QA, QC, Manufacturing & Process Development for PhD, M.Pharm, B.Pharm, M.Sc, B.Tech & M.Tech candidates.

Exciting Career Opportunities at Aragen Lifesciences – Biologics Division

Aragen Lifesciences, a globally recognized contract research and manufacturing services organization, invites talented professionals to be part of its expanding Biologics Division. Certified as a Great Place to Work (Feb 2025–Feb 2026), Aragen offers an exceptional work environment focused on innovation, growth, and employee wellbeing.

Walk-in interviews are scheduled for candidates looking to make a significant impact in biologics manufacturing and quality functions. Positions span across Downstream Manufacturing, Upstream Manufacturing, Analytical Development, Process Development, Quality Control, and Quality Assurance at their Bengaluru facility.

Departments & Open Positions

Departments Hiring:

• Downstream Manufacturing
• Upstream Manufacturing
• Downstream Process Development
• Upstream Process Development
• Analytical Development
• Quality Control (QC)
• Quality Assurance (QA)

Open Roles:

• Executive
• Senior Executive
• Deputy Manager
• Manager

Required Qualifications

Candidates must hold degrees in:

• Ph.D. in Biotechnology or related fields
• M.Pharm / B.Pharm
• M.Sc in Chemistry, Microbiology, or Biotechnology
• B.Tech / M.Tech in Biotechnology

Experience: 2 to 12 years in Biologics, GMP environments, or regulated bio-manufacturing operations.

Work & Interview Locations

Work Location:
Bommasandra, Bengaluru

Walk-In Interview Details:

• Date: 26th July 2025 (Saturday)
•  Time: 08:30 AM – 02:00 PM
•  Interview Address: Aragen Lifesciences Ltd, No. 12, Plot No. 28A, IDA, Nacharam – Mallapur Road, Yacharam, Hyderabad, Telangana 500076

Key Skills & Responsibilities

H3: Core Responsibilities Based on Department

H4: For Manufacturing Roles (Upstream/Downstream)

• Execution of production batches under cGMP compliance
• Equipment handling, process monitoring, and deviation control
• Buffer/media preparation and fermentation
• Aseptic techniques and cleanroom operations

H4: For Process Development (Upstream/Downstream)

• Development and scale-up of biologics processes
• Statistical process optimization and design of experiments (DoE)
• Collaboration with analytical and manufacturing teams

H4: For Quality Control & Assurance

• Analytical method development, transfer, and validation
• QA documentation, audit readiness, deviation and CAPA handling
• Microbiological and analytical testing of biologics products
• Ensuring regulatory compliance with USFDA, EMEA, and CDSCO

How to Apply

Walk-in candidates must register beforehand by scanning the QR code provided in the official job invitation. For more detailed job descriptions, candidates can visit Aragen’s careers page or scan the code for department-specific responsibilities.

For queries, reach out via official Aragen career channels.

Why Choose Aragen Lifesciences?

• Certified Great Place to Work
• Exposure to global projects in Biopharma
• Cutting-edge R&D and manufacturing infrastructure
• Career advancement and professional development programs

Apply Now – Step Into the Future of Biologics

Whether you’re a seasoned bio-manufacturing expert or a quality-focused scientist, Aragen Lifesciences offers the platform to grow, innovate, and lead.

Be part of a team that’s reshaping global healthcare—Join Aragen Lifesciences today!

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