CDSCO Scientific Officer Recruitment 2026
Looking for a prestigious Govt Life Science Job in India? The CDSCO Recruitment notification invites eligible candidates to apply for the post of Scientific Officer at the Regional Drugs Testing Laboratory (RDTL), Guwahati. If you have a postgraduate degree in Life Sciences, Pharmacy, Biotechnology, Microbiology, or related disciplines along with relevant experience, this Scientific Officer Job offers an excellent opportunity to contribute to India’s national drug quality and safety system while advancing your government research career.
About CDSCO
The Central Drugs Standard Control Organization (CDSCO) is India’s national regulatory authority for pharmaceuticals and medical devices functioning under the Directorate General of Health Services (DGHS), Ministry of Health & Family Welfare, Government of India. CDSCO is responsible for ensuring the safety, efficacy, and quality of drugs through regulatory approvals, inspections, laboratory testing, and scientific evaluation. Working with CDSCO provides professionals an opportunity to contribute to India’s healthcare and pharmaceutical regulatory ecosystem through meaningful scientific and regulatory work.
Job Details
| Company | Central Drugs Standard Control Organization (CDSCO) |
| Job Title | Scientific Officer (Group A) |
| Location | Regional Drugs Testing Laboratory (RDTL), Guwahati, Assam |
| Mode of Recruitment | Deputation (including Short-Term Contract) |
| Pay Level | Level 10 (₹56,100–1,77,500) |
| Maximum Age Limit | 56 years as on the closing date of application |
Role Overview
The Scientific Officer (Group A) will be responsible for scientific testing, drug analysis, and pharmaceutical standardization activities at RDTL Guwahati. Under the CDSCO Scientific Officer Recruitment framework, the selected candidate will contribute to laboratory-based drug testing, validation of analytical methods, regulatory compliance, and scientific documentation aligned with national quality standards. The role supports India’s regulatory system by ensuring pharmaceutical products meet safety, efficacy, and quality requirements.
Key Responsibilities
- Perform scientific testing, evaluation, and standardization of pharmaceutical products and drug samples.
- Support research activities related to drug quality, analytical methodologies, and pharmaceutical sciences.
- Ensure compliance with national regulatory standards, laboratory quality systems, and applicable government guidelines.
- Analyze laboratory data and prepare technical reports with scientific recommendations.
- Contribute to the development, validation, and implementation of analytical methods for drug testing.
- Maintain accurate scientific documentation and laboratory records as per regulatory requirements.
- Collaborate with regulatory authorities, research organizations, and stakeholders to support public health initiatives.
Eligibility Criteria
Service Requirements
- Holding an analogous post on a regular basis in the parent cadre or department; or
- Having two years of regular service in Pay Level 9 (₹53,100–1,67,800); or
- Having four years of regular service in Pay Level 8 (₹47,600–1,51,100).
Essential Qualifications
Master’s degree in any of the following disciplines from a recognized university or institute:
- Biochemistry
- Bacteriology
- Microbiology
- Biotechnology
Experience
- Minimum six years of experience in drug testing, pharmaceutical standardization, or scientific research related to pharmaceuticals.
Preferred Qualification
- Doctoral degree (Ph.D.) in Chemistry, Biochemistry, Pharmacy, Pharmaceutical Chemistry, Pharmacology, Bacteriology, Medicine, Microbiology, or Biotechnology from a recognized university or institute.
Key Competencies
- Strong expertise in pharmaceutical analysis and drug quality evaluation.
- Knowledge of drug testing methodologies, laboratory quality systems, and regulatory standards.
- Scientific research and analytical problem-solving skills.
- Technical report writing and scientific documentation.
- Effective communication and collaboration within multidisciplinary teams.
Application Process
Interested and eligible candidates should submit the prescribed application form along with supporting documents, including APAR/ACRs, Integrity Certificate, Vigilance Clearance Certificate, Cadre Clearance Certificate, and other required service records, within 60 days from the date of publication of the advertisement in Employment News.
Applications should be addressed to:
Deputy Director (Administration)
Central Drugs Standard Control Organization (CDSCO)
FDA Bhawan, Kotla Road
New Delhi – 110002
Why Join CDSCO?
Through the CDSCO Scientific Officer Recruitment, professionals gain the opportunity to work within India’s central drug regulatory authority. The role at RDTL Guwahati enables direct involvement in drug quality testing, regulatory compliance, and pharmaceutical standardization that support national public health objectives. This Govt Life Science Job provides exposure to regulatory science, laboratory systems, and pharmaceutical analysis within a structured government framework.
Conclusion
The CDSCO Scientific Officer Recruitment presents a valuable Govt Life Science Job opportunity for experienced professionals in pharmaceutical and life sciences disciplines. Eligible candidates should review the official notification and submit their applications within the prescribed timeline.
CLICK HERE FOR OFFICIAL NOTIFICATION
