- Full Time
- Bommasandra, Bengaluru,India
Website Aragen Lifesciences
Table of Contents
ToggleAbout Aragen Lifesciences
Aragen Lifesciences is a globally trusted R&D and manufacturing partner to the life sciences industry. With over two decades of experience, we specialize in contract research, development, and manufacturing services, focusing on early-stage discovery and development of New Molecular Entities (NMEs). From concept to commercial scale, we help transform ideas into impactful healthcare solutions.
Hiring For:
Executive / Sr. Executive / Deputy Manager / Manager
Departments:
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Upstream Manufacturing
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Downstream Manufacturing
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Analytical Development
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Upstream & Downstream Process Development
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Quality Control (QC)
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Quality Assurance (QA)
Educational Qualification:
Ph.D. / M.Pharm / B.Pharm
B.Tech / M.Tech – Biotechnology
M.Sc – Chemistry, Microbiology, Biotechnology
Experience: 2 to 12 Years
Job Location: Bommasandra, Bengaluru
Open Positions and Key Responsibilities
Analytical Development – Molecular Biology
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Hands-on experience in qPCR, RT-PCR, dPCR, DNA/RNA extraction, and gel electrophoresis.
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Method development and validation for molecular assays.
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Experience with mycoplasma detection, residual DNA testing, and viral safety assessment.
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Familiarity with regulatory standards and documentation practices.
Analytical Development – LC-MS
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Skilled in LC-MS/MS, UPLC-MS, Q-TOF, and Orbitrap systems.
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Method development and validation for biologics, biosimilars, and peptides.
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Proficiency in software like MassLynx, Skyline, OpenLab.
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Experience in intact mass analysis, glycan profiling, peptide mapping.
Downstream Manufacturing – Biologics
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Operate AKTA systems, chromatography columns, TFF units.
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Experience in depth filtration, column packing, and bioburden filtration.
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Responsible for documentation (BMRs, SOPs), safety compliance, and QMS.
Upstream Manufacturing – Biologics
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Execute mammalian cell culture in single-use bioreactors.
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Process optimization, equipment qualification, and troubleshooting.
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Maintain GMP compliance and in-process testing records.
Upstream Process Development & MSAT
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Design and execute scale-up/scale-down studies.
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Handle bioreactors (shake flask, Ambr, bench-top), media, and buffer prep.
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Collaborate with cross-functional teams for tech transfer and documentation.
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Ensure adherence to GXP, ALCOA, and EHSS standards.
Downstream Process Development & MSAT
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Plan DoE-based downstream studies using AKTA Pure, SDS-PAGE, Western Blotting.
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Perform tech transfer, equipment handling, and documentation.
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Maintain compliance with data integrity and regulatory expectations.
Downstream Process Development
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Manage and execute process development and tech transfer.
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Oversee equipment qualification (IQ/OQ/PQ), SOPs, and facility readiness.
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Coordinate consumable stock, team planning, and document verification.
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Handle change controls, troubleshooting, and regulatory inspections.
Quality Control – Digitalization & Bioassay
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Conduct biochemical and bioassay testing with real-time documentation.
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Maintain LIMS systems, manage calibration, CoA preparation, and equipment upkeep.
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Support method validations, deviation handling, and quality investigations.
In-Process Quality Assurance (IPQA)
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Perform real-time quality checks, line clearance, and batch record review.
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Approve protocols (e.g., process validation, gowning, cleaning).
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Lead investigations into non-conformances and ensure timely product release.
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Prepare APQR, handle audit responses, and maintain GMP compliance.
Walk-In Interview Details
📅 Date: 26th July 2025 (Saturday)
🕗 Time: 08:30 AM – 02:00 PM
📍 Venue: Aragen Lifesciences Ltd,
No. 12, Plot No. 28A, IDA, Nacharam – Mallapur Road,
Yacharam, Hyderabad, Telangana – 500076
Note to Candidates
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Bring updated CV, passport-sized photo, and last three months’ pay slips.
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Candidates unable to attend may send resumes to the HR contact at Aragen Lifesciences.
Shape the Future of Biologics with Aragen – Innovate, Develop, Deliver.
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