THSTI Quality Assurance Associate Documentation Officer Project Research Scientist Recruitment 2026

Earn Rs. 56,000 to Rs. 60,000 per month working at one of India's leading biotech research institutes under the Department of Biotechnology (DBT), Government of India. BRIC-Translational Health Science and Technology Institute (THSTI) is hiring for 3 contract posts at its NCR Biotech Science Cluster campus in Faridabad, Haryana. These are project-based positions ideal for science graduates with laboratory or data management experience.

Available Posts

Key Highlights

• Contract posts under CEPI and GRASPP research projects — not permanent government positions
• QA Associate and Documentation Officer roles need GCP/GLP/NABL knowledge — lab compliance background is a strong advantage
• Project Research Scientist-I (Data Manager) is open to freshers — experience in R/Python/STATA is desirable, not mandatory
• All 3 posts are based at Faridabad, Haryana — no all-India posting
• Women candidates pay a reduced fee of Rs. 118 — regardless of category
• No hard copy submission needed — the entire process is online including fee payment

Selection Process

Applications go through an initial scrutiny and shortlisting round. THSTI then calls shortlisted candidates for a written test, skill test, or interview — or a combination of these — based on the number of eligible applications received. The institute's decision on which stages apply is final, so be prepared for any of these rounds.

Preparation Tips for THSTI Recruitment 2026

• For QA Associate and Documentation Officer: brush up on Quality Management Systems (QMS), GCP, GLP, and NABL/ISO accreditation processes — these are the core competencies being assessed
• Review SOPs, deviation handling, and CAPA procedures — these are directly listed in the job requirements
• For Project Research Scientist-I: revise clinical data management concepts and database administration basics
• Practise with R, Python, or STATA if you have exposure — the notification lists these as desirable skills
• Download the official notification PDF from thsti.res.in and review the detailed eligibility before your interview
• Check your email regularly — THSTI communicates all updates (shortlisting, interview calls) only via email

Documents You'll Need

Keep these ready before you start your online application:

• Passport-size photo and scanned signature in JPEG/JPG/PNG format
• Educational certificates (10th, 12th, graduation/post-graduation degree and mark sheets)
• Experience certificates relevant to the post you are applying for
• Caste or disability certificate in the Government of India format (if claiming reservation)

See the complete document list in the section below.

Frequently Asked Questions

Q. What is the last date to apply for THSTI Recruitment 2026?

A. The last date to apply for THSTI Quality Assurance Associate, Documentation Officer, and Project Research Scientist-I is 23 March 2026. You can apply online through recruitment.thsti.in.

Q. What qualification do I need for THSTI Quality Assurance Associate or Documentation Officer?

A. You need either a graduation in any branch of Science with at least 3 years of relevant experience, or a post-graduation in Science with at least 1 year of experience. GCP/GLP laboratory experience is preferred.

Q. Are THSTI posts permanent government jobs?

A. No — all 3 posts are contract-based project positions. They are not permanent government posts and are not under the 7th Central Pay Commission pay matrix.

Q. Can freshers apply for THSTI Project Research Scientist-I (Assistant Data Manager)?

A. Yes, freshers can apply. A post-graduation or B.E./B.Tech in Computer Science, Computer Application, or Data Science is the minimum requirement. Experience in clinical data management is desirable but not mandatory.

• Quality Assurance Associate
• Implement and maintain Quality Management Systems (QMS) in clinical trial sample testing and bioanalytical laboratories
• Review and control SOPs, laboratory documents, LIMS entries, deviations, and corrective and preventive actions (CAPAs)
• Ensure compliance during receipt, testing, storage, and disposal of clinical trial samples
• Support internal audits, sponsor audits, and regulatory inspections including audit preparation and follow-up
• Apply working knowledge of GCP, GLP, and NABL/ISO standards to day-to-day laboratory operations

• Documentation Officer
• Prepare, review, issue, and version-control SOPs, manuals, formats, and records as per QMS requirements
• Maintain archival and retrieval systems for laboratory and clinical trial documentation
• Apply working knowledge of GCP, GLP, GDP, and regulatory documentation practices
• Keep accurate and complete records in compliance with NABL or ISO accreditation requirements
• Support integration of document management systems (IMS) where applicable

• Project Research Scientist-I (Assistant Data Manager)
• Manage clinical research databases and assist in database administration
• Prepare Clinical Study and Data Management documents
• Perform software validation and maintain related documentation
• Develop and maintain clinical databases using standard tools
• Maintain server and hardware systems and provide IT support to the research team
• Work with programming tools such as R, Python, or STATA for data processing and analysis