Veeda CR is conducting a walk-in interview in Ahmedabad for multiple positions across Bioanalytical Research, Clinical Operations, Information Communication Technology (ICT), Enterprise Digital Transformation, and Quality Assurance. The recruitment drive includes opportunities for freshers and experienced candidates, with qualifications ranging from B.Pharm, M.Pharm, B.Sc. and M.Sc. to Pharm.D, B.Tech, B.E., BCA, MCA and M.Sc. IT.
Veeda CR Walk-In Interview 2026: Job Details
| Particulars | Details |
|---|---|
| Company | Veeda CR |
| Recruitment Type | Walk-In Interview |
| Total Openings | 20 |
| Job Location | Ahmedabad, Gujarat |
| Experience | Freshers to 6 years, depending on the role |
| Employment Type | Full-time, Permanent |
| Walk-In Date | 1 November 2026 |
| Interview Time | 10:00 AM – 3:00 PM |
| Contact Person | Vismay Vora |
Walk-In Interview Date, Time and Venue
Date: 1 November 2026
Time: 10:00 AM to 3:00 PM
Venue: Satyamev Corporate, Opp. Prahalad Nagar Fire Station, near Shalin Bungalows, Corporate Road, Prahalad Nagar, Ahmedabad, Gujarat – 380015.
Location: View Venue on Google Maps
Positions Available at Veeda CR
1. Bioanalytical Research Department
| Position | Experience | Qualification |
|---|---|---|
| Analyst | Freshers | B.Pharm, M.Pharm, M.Sc. |
| Senior Analyst | 1–3 years | B.Pharm, M.Pharm, M.Sc. |
| Junior Group Leader | 3–6 years | B.Pharm, M.Pharm, M.Sc. |
| Instrumentation Engineer | 2–5 years | B.Pharm, M.Pharm, M.Sc. |
| Custodian | Freshers | B.Pharm, M.Pharm, B.Sc., M.Sc. |
Key Responsibilities:
- Senior Analyst: Sample processing, LC-MS and ICP-MS.
- Junior Group Leader: Sample processing, LC-MS, ICP-MS and instrument operation.
- Instrumentation Engineer: Routine inspections, calibration and preventive maintenance of laboratory instruments and equipment.
- Custodian: Handling, storage, documentation and disposal of biological samples, chemicals and laboratory materials in compliance with GLP, GCP and regulatory guidelines.
2. Clinical Operations Department
| Position | Experience | Qualification |
|---|---|---|
| Clinical Trial Assistant (CTA) | 0–2 years | B.Pharm, M.Pharm, Pharm.D |
| Clinical Research Associate (CRA) | 3–5 years | B.Pharm, M.Pharm, Pharm.D, M.Sc. in Clinical Research |
Key Responsibilities:
Clinical Trial Assistant (CTA)
- Manage clinical trial documentation and study archives.
- Prepare site initiation visit (SIV) kits.
- Coordinate investigational medicinal product (IMP) and sample logistics.
- Handle site payments, phlebotomist coordination and MIS trackers.
Clinical Research Coordinators are also suitable for the CTA role.
Clinical Research Associate (CRA)
- Conduct site feasibility, initiation, monitoring and closeout visits.
- Train site personnel.
- Maintain study documentation.
- Ensure compliance with study protocols, GCP, SOPs and regulatory requirements.
3. Information Communication Technology (ICT) Department
| Position | Experience | Qualification |
|---|---|---|
| IT Administrator | 2–6 years | B.Tech, M.Tech, B.E., M.E., BCA, MCA |
Key Requirements:
- IT infrastructure and server administration.
- Backup and recovery.
- Team management.
- Experience with regulated systems in the pharmaceutical or life sciences industry.
4. Enterprise Digital Transformation Department
| Position | Experience | Qualification |
|---|---|---|
| Software Developer | 3–6 years | B.Tech, M.Tech, B.E., M.E., BCA, MCA |
Key Responsibilities:
- Develop, fine-tune and deploy Generative AI models.
- Work with Python, large language models (LLMs), retrieval-augmented generation (RAG) and AI frameworks.
- Build, integrate and optimise AI-powered applications.
5. Quality Assurance Department
| Position | Experience | Qualification |
|---|---|---|
| Bioanalytical Research QA | 4–6 years | B.Pharm, M.Pharm, M.Sc. |
| Clinical Research QA | 1–2 years | B.Pharm, M.Pharm, M.Sc. |
| Quality Management System QA (CRQA) | 2–4 years | B.Pharm, M.Pharm, M.Sc. |
| Quality Management System QA (CSV IT) | 4–6 years | M.Sc. IT or relevant fields |
Key Requirements by Role:
Bioanalytical Research QA
- GLP/GCP regulations and regulatory guidelines.
- QA auditing and CAPA management.
- QMS processes, SOP review and deviation investigation.
- Bioanalytical and analytical study audits.
Clinical Research QA
- ICH-GCP, Indian GCP and BA/BE studies.
- Clinical trial and Trial Master File (TMF) audits.
- Essential document review.
- CAPA, deviation and change control management.
- QMS and regulatory compliance.
Quality Management System QA (CRQA)
- QMS, CAPA, change control and deviation management.
- System and vendor audits.
- Computerized System Validation (CSV).
- Data integrity, GCP/GLP/CDSCO compliance and SOP management.
- Inspection readiness.
Quality Management System QA (CSV IT)
- QMS processes, CAPA, change control and deviation management.
- System and vendor audits.
- Computerized System Validation (CSV) and data integrity.
- Regulatory compliance, SOP management and inspection readiness.
Eligibility and Qualifications
Candidates can apply according to the educational requirements and experience specified for each position.
- Pharmacy: B.Pharm, M.Pharm, Pharm.D.
- Life Sciences: B.Sc., M.Sc.
- Clinical Research: M.Sc. in Clinical Research.
- Information Technology: BCA, MCA, M.Sc. IT or relevant fields.
- Engineering: B.E., B.Tech, M.E., M.Tech.
Freshers can apply for the Analyst and Custodian positions. Other roles require relevant experience ranging from 1 to 6 years, depending on the position.
Required Skills
The recruitment drive covers the following technical and professional skills:
- LC-MS and ICP-MS.
- Sample processing and instrument calibration.
- Clinical trial documentation and clinical operations.
- Clinical research and GCP compliance.
- IT infrastructure and server administration.
- Python, LLMs, RAG and Generative AI development.
- Quality assurance, QMS and CAPA management.
- GLP, GCP, CDSCO compliance and regulatory documentation.
- Computerized System Validation and data integrity.
How to Attend the Veeda CR Walk-In Interview
Eligible candidates should attend the walk-in interview at the venue and during the time mentioned above, selecting a position that matches their qualifications and experience.
Contact Person: Vismay Vora.
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Location: View Venue on Google Maps
