Associate – Quality Control Analytical/ In Process – HPLC / Instrumentation (Biosimilars)

Biopatrika; Hyderabad; On-site; INR 500,000 - 800,000; Full time

Job summary

DrReddy’s Laboratories Limited in Hyderabad, India is seeking an Associate for Quality Control Analytical/In Process with HPLC instrumentation expertise. The role requires 2–6 years of experience in biosimilars analytics and a Master’s degree in Life Sciences.

You will perform analytical testing, validate chromatographic methods, and ensure cGMP/GDP/GAP compliance while supporting audits and regulatory inspections.

Qualifications

• Master’s degree in Life Sciences required.
• 2–6 years of QC Analytical experience in biosimilars/biologics.
• Experience with RP-HPLC, SEC, IEX, glycan analysis, and peptide mapping.
• Method validation for biosimilar products.
• QC analytical testing of drug substances and drug products.
• Knowledge of cGMP, GDP, GAP and regulatory compliance.
• Audit readiness and quality systems documentation.

Responsibilities

• Perform analytical testing of Biosimilar/Biologics drug substances, drug products, in-process, and stability samples.
• Execute chromatography-based analyses and analytical method validation activities.
• Ensure compliance with cGMP, Good Documentation Practices, Good Analytical Practices, and internal SOPs.
• Support regulatory inspections, audit readiness activities, and quality compliance initiatives.
• Maintain laboratory safety standards and adhere to established safety procedures.

Education

Master’s degree in Life Sciences

Tools

HPLC Instrumentation

Job description

# Associate – Quality Control Analytical/ In Process – HPLC / Instrumentation (Biosimilars)JobHyderabad, IndiaOctober 1, 2026Full Time### Job Overview* Date Posted October 1, 2026* Location Hyderabad, India* Expiration date October 31, 2026* Click to apply: https://jobs.smartrecruiters.com/ni/DrReddysLaboratoriesLimited/f2718db8-8a46-4ed0-b16d-3281ed902d86-quality-control-associate### Job DescriptionWere Hiring | Associate – Quality Control Analytical/ In Process – HPLC / Instrumentation (Biosimilars) Are you passionate about analytical sciences and quality excellence in biologics? Join our Quality Control Analytical team and contribute to ensuring the quality, safety, and compliance of Biosimilar products through advanced analytical testing and regulatory adherence. Location: Hyderabad Experience: 2-6 Years Qualification: Master’s in any Life Sciences Key Skills & Expertise RP-HPLC, SEC, IEX, Glycan Analysis amp; Peptide Mapping Method Validation for Biosimilar Products QC Analytical Testing of Drug Substance amp; Drug Product Samples cGMP, GDP, GAP amp; Regulatory Compliance Audit Readiness, Documentation amp; Quality Systems Key Responsibilities • Perform analytical testing of Biosimilar/Biologics drug substances, drug products, in-process, and stability samples. • Execute chromatography-based analyses and analytical method validation activities. • Ensure compliance with cGMP, Good Documentation Practices, Good Analytical Practices, and internal SOPs. • Support regulatory inspections, audit readiness activities, and quality compliance initiatives. • Maintain laboratory safety standards and adhere to established safety procedures. If you have hands-on experience in Biosimilar analytical testing and are looking to advance your career in a dynamic biologics environment, wed love to connect with you. Apply now or share your profile with your network. https://smrtr.io/C6KKV