Government Pharma Jobs at Department of Pharmaceuticals | Pharmacy Graduates Eligible
Are you looking for high-paying government pharma jobs? The Department of Pharmaceuticals Recruitment 2026 invites eligible professionals to apply for the Technical Expert (Pharma) position under the PRIP Scheme. Selected candidates will receive ₹80,000 to ₹1,45,000 per month, and applications must be submitted by 11 August 2026.
Job Details
- Advertisement No: 02/2026
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Job Positions:
- Programme Lead – Senior Consultant
- Technical Expert Grade 2 (Pharma)
- Technical Expert (Pharma)
- Maximum Age Limit: 50 years as on 31 March 2026
- Last Date for Receipt of Application: 11 August 2026
- Remuneration: ₹80,000 – ₹1,45,000 per month
About the Department of Pharmaceuticals
The Department of Pharmaceuticals (DoP) operates under the Ministry of Chemicals and Fertilizers, Government of India. It plays a pivotal role in the development and regulation of the pharmaceutical sector, aiming to enhance innovation and research in the Pharma MedTech space. The DoP is committed to promoting research initiatives that align with national health objectives, making it a significant player in the government pharma jobs landscape.
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Positions Available
1. Programme Lead – Senior Consultant
- Division: Academia and Research Division
- Number of Positions: One (Whole Time)
- Maximum Age Limit: Not more than 62 years as on 31.03.2026.
- Remuneration: ₹ 2,65,000 – ₹ 3,30,000 per month (Fixed).
Key Responsibilities
- Overall Management: Act as overall manager of the PMU which may include other resources.
- Governance & Secretariat: Plan and run meetings of TC/PAAC/EC: Agendas/briefs, minutes, decision registers, and action tracking to closure. Secretariat interface with PMA; ensure timely circulation of notes and consolidated reviews.
- Programme Management: Steer the workflow application using the portal: PMA Screening → DoP approval → technical review → PAAC approval → agreement → milestone/disbursal → monitoring → closure, with clear SOPs. Oversee evaluation logistics (expert empanelment, relevant disclosure compliance, assignment of reviews). Manage extension/variance and over/under-utilisation cases; recommend site/virtual reviews as needed.
- Financial & Legal Interfaces: Coordinate milestone-linked fund disbursals with checks per GFR/DFPR; align with PFMS/BharatKosh processes; Liaise with Finance/Legal on agreements, breach/termination, recovery/clawback, and contracting issues.
- Coordination & Stakeholder Engagement: Act as a single point between DoP, PMA, TC, PAAC, expert panels, and applicants; convene consultations/outreach as required.
- Digital, MIS & Reporting: Own dashboards and data quality on the portal/MIS; publish monthly/quarterly KPI reports and narrative updates; maintain audit-ready records.
- Risk & Compliance: Implement confidentiality/disclosures controls; ensure documentation for internal/external audits; maintain decision trails.
Qualifications & Experience
- Qualification: Graduate degree in Management/Engineering/Pharma/Health/Public Policy or a related field. (Desirable: Post-graduate degree).
- Experience: 15+ years of experience leading a PMU/program delivery (public or private sector) in R&D/innovation, health, or drug/medical device development.
- Core Knowledge: Governance & secretariat, Digital & MIS, Financial & legal interfaces, and MS Office Suite (Advanced Excel/PowerPoint).
2. Technical Expert Grade 2 (Pharma)
- Division: Academia and Research Division
- Number of Positions: One (Full-Time)
- Maximum Age Limit: Not more than 50 years as of 31.03.2026.
- Remuneration: ₹ 1,45,000 – ₹ 2,65,000 per month (Fixed).
Key Responsibilities
- Technical Appraisal & Recommendations: Conduct desk reviews of applications; review screening and parameter-based scoring; prepare technical appraisal notes and recommendations for TC/PAAC. Assess scientific merit, novelty/FTO (basic), feasibility, team capability, development risks, and alignment to PRIP priority/SPI areas.
- Milestone Design & Regulatory Alignment: Ensure alignment with applicable regulatory and quality frameworks (ND&CT Rules 2019, Drugs & Cosmetics Act, Medical Devices Rules) governing clinical and ethical practices. Confirm supporting documentation is complete and sufficient for evaluation.
- Budget & Plan Due Diligence: Review project plans for cost rationality, resource realism, co-funding evidence, and adherence to scheme expenditure guardrails; suggest re-phasing where required.
- Monitoring & Disbursals: Review progress reports; examine extension/variance and over/under-utilisation requests; recommend milestone disbursals/withholds. Undertake site/virtual visits and third-party validations.
- Coordination & Quality: Work with PMA, NIPERs, TC and empanelled experts for assignments, relevant disclosure checks, and consolidation of reviews. Contribute to SOPs/templates, reviewer manuals, and MIS field refinements.
- Capacity Building & Queries: Support onboarding/orientation of reviewers; provide clarifications on technical queries from DoP/TC/PMA.
Qualifications & Experience
- Qualification: Graduate degree (B.Pharm/BSc/BTech) in Pharmaceutical Sciences / Medicinal Chemistry / Pharmacology / Biotech or related field; or equivalent qualification with strong relevant experience. (Desirable: Post-graduate degree M.Pharm/MSc/MTech/MS/MD/PhD).
- Experience: 8- 15 years post-qualification experience across drug R&D (discovery, pre-clinical, clinical and/or CMC) in industry/CRO/academia or government programmes. Demonstrated capability to appraise R&D proposals and define TRL-based milestones.
- Core Knowledge: Proposal appraisal, Regulatory fluency (Indian pathways – CDSCO / New Drugs & CT Rules), basics of GMP/QMS, and MS Office Suite.
3. Technical Expert (Pharma)
- Division: Academia and Research Division
- Number of Positions: One (Full-Time)
- Maximum Age Limit: Not more than 50 years as of 31.03.2026.
- Remuneration: ₹ 80,000 – ₹ 1,45,000 per month (Fixed).
Key Responsibilities
- Technical Appraisal & Recommendations: Conduct desk reviews of applications; review screening and parameter-based scoring; prepare technical appraisal notes and recommendations. Assess scientific merit, novelty/FTO (basic), feasibility, team capability, development risks, and alignment to PRIP priority.
- Milestone Design & Regulatory Alignment: Ensure alignment with applicable regulatory frameworks (ND&CT Rules 2019, Drugs & Cosmetics Act, etc.).
- Budget & Plan Due Diligence: Review project plans for cost rationality, resource realism, and adherence to scheme expenditure guardrails.
- Monitoring & Disbursals: Review progress reports; examine extension/variance requests; recommend milestone disbursals. Undertake site/virtual visits as advised.
- Coordination & Quality: Work with PMA, NIPERs, TC, and empanelled experts. Contribute to SOPs/templates, reviewer manuals, and MIS refinements.
- Capacity Building & Queries: Support onboarding/orientation of reviewers; provide clarifications on technical queries.
Qualifications & Experience
- Qualification: Graduate degree (B.Pharm/BSc/BTech) in Pharmaceutical Sciences / Medicinal Chemistry / Pharmacology / Biotech or related field; or equivalent. (Desirable: Post-graduate degree).
- Experience: 3- 8 years post-qualification experience across drug R&D (discovery, pre-clinical, clinical and/or CMC) in industry/CRO/academia or government programmes.
- Core Knowledge: Proposal appraisal, Regulatory fluency, basics of GMP/QMS, and MS Office Suite.
Documents Required
- Completed application form.
- Relevant educational and experience certificates.
- Any other documents as specified in the application guidelines.
How to Apply
Applications must be submitted using the prescribed form available online. Completed applications should be sent via:
- Hard Copy: To the Office of the Under Secretary (E&A), Department of Pharmaceuticals, G-19, Shastri Bhawan, New Delhi.
- Email: SO-Establishment@pharma-dept.gov.in
For more details, visit the official website: LINK
CLICK HERE FOR THE ORIGINAL NOTIFICATION
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In summary, the Department of Pharmaceuticals is offering government pharma jobs that provide a substantial salary and a chance to make a significant impact in the healthcare sector. Eligible candidates are encouraged to apply for this role before the deadline of 11 August 2026. This position not only promises a rewarding career but also an opportunity to contribute to the advancement of pharmaceutical research and innovation.
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