Vivo Bio Tech Walk-in Research, Toxicology, Bioanalytical, and QA
- Company Overview
- Walk-in Drive Details
- Job Role & Responsibilities
- Research Associate (Freshers)
- Study Director – Toxicology / Bioanalysis / ADME
- Veterinarian / Animal House Veterinarian
- Quality Assurance Auditor
- Eligibility / Qualifications
- Location & Salary
- Application Process
- Why Join Vivo Bio Tech
- FAQs
MSc, M.Pharm Openings – Vivo Bio Tech Walk-in Drive Hyderabad 2025
Vivo Bio Tech hiring MSc, M.Pharm, BVSc candidates for Research, Toxicology, Bioanalytical, and QA roles. Walk-in Hyderabad, 14th Nov 2025.
Vivo Bio Tech Ltd, a leading CRO and preclinical research organization, is conducting a Walk-in Drive on 14th November 2025 (Friday) for multiple positions across departments at its Pregnapur facility, Hyderabad. This is an excellent opportunity for Life Sciences, Pharmacy, and Veterinary Science graduates to build their careers with an OECD GLP-certified, CPCSEA-accredited preclinical research company.
Company Overview
Vivo Bio Tech Ltd. is a reputed Contract Research Organization (CRO) providing comprehensive preclinical research, toxicology, and bioanalytical services to global pharmaceutical and biotechnology companies. With OECD GLP, CPCSEA, ISO 9001:2015, and CIBRC certifications, Vivo Bio Tech upholds international standards of quality, ethics, and scientific excellence.
Established as a trusted partner for drug discovery and safety evaluation, the company operates world-class facilities equipped for toxicology, pharmacology, ADME, and bioanalysis studies. Vivo Bio Tech’s scientific expertise supports innovation in life sciences while ensuring regulatory compliance and data integrity.
Walk-in Drive Details
Date: Friday, 14th November 2025
Time: 10:00 AM to 3:00 PM
Venue: Vivo Bio Tech Ltd, 3rd Floor, Ilyas Mohammed Khan Estate, Beside Bajaj Electronics, Road No. 01, Banjara Hills, Hyderabad – 500034, Telangana
Work Location: Pregnapur Village, Gajwel Mandal, Siddipet District, Telangana
Website: www.vivobio.com
Job Role & Responsibilities
Research Associate (Freshers)
- Conduct laboratory-based preclinical research and experimental studies.
- Support ongoing toxicology and pharmacology projects.
- Assist study directors and QA teams with documentation and reporting.
Study Director – Toxicology / Bioanalysis / ADME
- Design and conduct GLP-compliant studies in respective areas.
- Prepare study plans, reports, and regulatory documentation.
- Ensure scientific accuracy, data integrity, and adherence to SOPs.
- Coordinate with clients, technical staff, and QA auditors.
Veterinarian / Animal House Veterinarian
- Oversee animal welfare and preclinical study compliance under CPCSEA.
- Conduct clinical observations, health assessments, and necropsy procedures.
- Maintain records of animal husbandry and study-related activities.
Quality Assurance Auditor
- Audit study documentation, data, and reports for GLP compliance.
- Participate in internal and external quality audits.
- Review protocols, raw data, and final reports.
- Provide QA oversight for all study phases.
Eligibility / Qualifications
Educational Requirements:
- M.Sc (Life Sciences, Biotechnology, Microbiology, Biochemistry, Zoology, Pharmacology)
- M.Pharm (Pharmaceutics, Pharmacology, Pharmaceutical Analysis)
- B.V.Sc / M.V.Sc (Veterinary Science, Toxicology, Animal Science)
Experience Range:
- Freshers to 7 years (varies by position)
Relevant Courses (comma-separated):
M.Sc Life Sciences, M.Pharm Pharmacology, B.V.Sc, M.V.Sc, Diploma in Toxicology, Certificate in GLP, Regulatory Compliance Training, Bioanalytical Method Development.
Key Skills:
- GLP/GCP Compliance
- Preclinical Study Design & Execution
- Toxicology & Pharmacokinetics
- Data Documentation & Quality Assurance
- Animal Welfare & CPCSEA Guidelines
Location & Salary
Work Location: Pregnapur, Siddipet District, Telangana
Interview Venue: Hyderabad, Telangana
Employment Type: Full-time, On-site
Compensation: Competitive salary based on experience and role.
Benefits: Health insurance, transport, subsidized canteen, and growth opportunities in a GLP-certified environment.
Application Process
Interested candidates can attend the walk-in interview with the following documents:
- Updated Resume
- Educational Certificates
- Experience Letters (if applicable)
- Passport-size Photograph
- Government ID Proof
Email: hr@vivobio.com
Contact: +91 40 2340 1234
Website: www.vivobio.com
Candidates with prior experience in GLP, CRO, or preclinical research environments will be given preference.
Why Join Vivo Bio Tech
- Work with one of India’s leading OECD GLP-certified CROs.
- Contribute to global preclinical and toxicology studies supporting pharmaceutical innovation.
- Opportunity to learn from experienced scientists and veterinarians.
- Strong focus on ethical animal research and regulatory compliance.
- A culture that fosters learning, innovation, and scientific integrity.
FAQs
Q1. What qualifications are required to apply?
A1. M.Sc, M.Pharm, B.V.Sc, or M.V.Sc in relevant fields such as Life Sciences, Toxicology, or Pharmacy.
Q2. Is prior experience mandatory?
A2. Freshers are eligible for Research Associate roles; other roles require 2–7 years of experience.
Q3. Where is the work location?
A3. The facility is located at Pregnapur, Siddipet District, Telangana.
Q4. Are the positions full-time?
A4. Yes, all positions are full-time, on-site roles.
Q5. What certifications does Vivo Bio Tech hold?
A5. Vivo Bio Tech is OECD GLP Certified, CPCSEA Accredited, CIBRC/DCA Approved, and ISO 9001:2015 Certified.
| Company | Vivo Bio Tech Ltd. |
|---|---|
| Vacancies | 48 (Across 7 Departments) |
| Required Education | M.Sc, M.Pharm, B.V.Sc, M.V.Sc |
| Experience | Freshers – 7 Years |
| Location | Pregnapur, Siddipet District, Telangana |
