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Veeda Lifesciences, a leading global Contract Research Organization (CRO), is conducting a walk-in interview for freshers to join its Bioanalytical Research & Quality teams at Ahmedabad. This is an excellent opportunity for candidates looking to start a career in bioanalysis, regulatory compliance, and scientific documentation.
About Company
Veeda Lifesciences is a global CRO offering comprehensive clinical, preclinical, and bioanalytical services to support the development of innovative, biosimilar, and generic drugs.
The organization has strong expertise in preclinical R&D, BA/BE studies, bioanalytical services, and Phase I–IV clinical trials. Known for its scientific excellence, regulatory compliance, and ethical practices, Veeda continuously invests in people, processes, and advanced technologies to deliver high-quality and globally compliant research solutions.
Job Details
- Company Name: Veeda Lifesciences
- Job Roles:
- Analyst
- Bioanalytical Quality Management (BQM)
- Report Writer
- Experience Required: 0 Years (Freshers)
- Total Vacancies: 15
- Salary Package: ₹2.5 – 3.5 LPA
- Job Location: Ahmedabad
Walk-In Interview Details
- Date: 21st December
- Time: 9:30 AM – 2:30 PM
- Venue:
Satyamev Corporate, Corporate Road,
Near Shalin Bungalows, Opp. Prahalad Nagar Fire Station,
Prahalad Nagar, Ahmedabad, Gujarat – 380015 - Contact Person: Vismay Vora
Job Responsibilities
Analyst
- Perform bioanalytical analysis of biological samples such as plasma, serum, urine, and tissue.
- Operate analytical instruments including LC-MS/MS and HPLC.
- Support method development, optimization, and validation as per US FDA, EMA, and GLP guidelines.
- Conduct sample preparation, extraction, and data acquisition.
- Maintain accurate analytical records, raw data, and laboratory notebooks.
BQM (Bioanalytical Quality Management)
- Review bioanalytical data including chromatograms, calibration curves, and QC samples.
- Review BMV, partial validation, and cross-validation reports.
- Ensure compliance with GLP, GCP, US FDA, EMA, and CDSCO requirements.
- Verify data integrity (ALCOA+) and traceability of data.
- Review study plans, SOPs, protocols, and amendments.
Report Writer
- Prepare bioanalytical study reports including method validation, sample analysis, and stability reports.
- Compile and interpret analytical data from LC-MS/MS and other platforms.
- Ensure reports comply with GLP, GCP, FDA, EMA, and ICH guidelines.
- Review raw data, calculations, chromatograms, and tables for accuracy.
- Maintain proper documentation, version control, and archival of reports.
- Coordinate with Analysts, QA, and Study Directors to resolve data queries.
Who Can Apply
- Freshers with interest in Bioanalytical Research, Quality Management, or Regulatory Documentation
- Candidates with basic knowledge of LC-MS/MS, HPLC, GLP, and GCP
- Good documentation and communication skills
📌 Interested candidates can attend the walk-in interview directly with updated CV and relevant documents.
