Vivo Biotech Ltd., a leading Contract Research Organization (CRO), is seeking experienced professionals in Toxicology, Bio Analytical, and Analytical Chemistry for various positions at their Pregnapur facility near Hyderabad. If you have experience in a GLP (Good Laboratory Practice) environment apply now
Vivo Bio Tech Hiring for Business Development (Freshers Also Welcome)[/caption]
About Vivo Biotech
Vivo Biotech Ltd. is a renowned name in the CRO industry, providing comprehensive drug discovery and development solutions to global clients. The company is known for its focus on innovation, compliance with international standards (OECD, CPCSEA, DSIR), and state-of-the-art infrastructure. Located in Pregnapur, Siddipet District, Telangana, the organization continues to grow and seeks talented professionals to contribute to its mission.Current Openings – Vivo Biotech Hyderabad
Vivo Biotech is hiring for the following positions in its Toxicology, Bio Analytical, and Analytical Chemistry departments:1. Study Director - Analytical Chemistry
- Qualification: MSc Life Sciences / M Pharm
- Experience: 4-16 years
- Job Description: Responsible for overseeing analytical chemistry studies and ensuring compliance with GLP guidelines. You will lead and execute critical experiments for drug discovery and development.
2. Study Director - Toxicology (General & Inhalation)
- Qualification: MSc Life Sciences / M Pharm
- Experience: 4-7 years
- Job Description: In this role, you will manage toxicology studies, including both general toxicology and inhalation toxicology. You will ensure that all studies are performed in accordance with regulatory guidelines and produce high-quality data for submission.
Vivo Bio Tech Hiring for Business Development (Freshers Also Welcome)[/caption]
3. Study Director - Bio Analytical
- Qualification: MSc Life Sciences / M Pharm
- Experience: 5-12 years
- Job Description: As the Study Director for Bio Analytical, you will focus on bioanalytical testing, particularly bioanalysis of drugs in biological matrices. You will oversee assay development and validation in compliance with GLP standards.
