Development Quality Assurance (DQA) – Biologics

Biopatrika; Hyderabad; On-site; INR 900,000 - 1,300,000; Full time

Job summary

Biopatrika in Hyderabad seeks a Development Quality Assurance (DQA) professional with Biologics Analytical Development expertise to support data review, method qualification, tech transfer, and stability studies.

The role requires a Master’s in Life Sciences and 3–7 years in biopharma, with hands-on work in HPLC/UPLC/LC-MS/UV-Vis, and strong GMP, data integrity, CAPA and audit management knowledge. Location: Bachupally, Hyderabad.

Qualifications

• Master’s in Life Sciences or related field is required.
• 3–7 years in the biopharmaceutical industry with focus on product development and quality management.
• Hands-on exposure to HPLC, UPLC, LC-MS, UV-Vis and related analytical techniques.

Responsibilities

• Support analytical data review, method qualification, technology transfer, stability studies and compliance activities.
• Ensure GMP, data integrity, CAPA, Change Controls and Audit Management are applied during development QA processes.

Skills

GMP knowledge

Data Integrity

CAPA

OOS

Change Controls

Audit Management

QMS

Education

Master’s in Life Sciences

Tools

HPLC

UPLC

LC-MS

UV-Vis

Job description

# Development Quality Assurance (DQA) – BiologicsJobHyderabad, IndiaOctober 5, 2026Full Time### Job Overview* Date Posted October 5, 2026* Location Hyderabad, India* Expiration date November 4, 2026* Click to apply: https://www.linkedin.com/posts/natasha-pillay-92677414a\\_hiring-dqa-developmentqualityassurance-share-7511345161281511424-6Dw2/### Job DescriptionHiring | Development Quality Assurance (DQA) – Biologics Were looking for a Development Quality Assurance (DQA) professional with expertise in Biologics Analytical Development, GMP, Data Integrity, and QMS to support analytical data review, method qualification, technology transfer, stability studies, and compliance activities. Location: Bachupally, Hyderabad Qualification: Master’s in (Life Sciences, Biotechnology, Biochemistry, Microbiology, or related disciplines) Experience: 3-7 Years experience in the Biopharmaceutical industry, with a focus on product development and quality management Experience in Analytical DQA / Development QA Hands-on exposure to HPLC, UPLC, LC-MS, UV-Vis, and related analytical techniques Knowledge of GMP, Data Integrity, CAPA, OOS, Change Controls amp; Audit Management Interested candidates can apply : https://smrtr.io/C6PCg