VIMTA Labs Hiring for Group Leader, Research Scientist & Trainee Roles in Preclinical Division

Join VIMTA Labs Preclinical Division for exciting preclinical jobs in bioanalysis, toxicology, and DART studies. Opportunities for freshers and experienced professionals in India’s leading CRO. Apply now!

About the Company

VIMTA Labs, established in 1984, is a leading contract research and testing organization headquartered in Hyderabad, India. Driven by the motto “Driven by Quality. Inspired by Science,” the company offers comprehensive preclinical, clinical, and analytical services.

With GLP-certified facilities since 2011, multiple international accreditations (including WHO prequalification), and a global client base, VIMTA specializes in high-quality preclinical research for pharmaceutical and biotech industries.

Job Details

• Company Name: VIMTA Labs
• Experience: Fresher to 10–15 years (varies by role)
• Qualification: M.Sc (Zoology), M.Pharm (Pharmacology/Toxicology); advanced degrees implied for senior roles
• Work Type: On-site

Job Description

VIMTA Labs is expanding its Preclinical Division and inviting applications for key roles in bioanalytical and toxicology research.

These positions offer exposure to cutting-edge GLP/GCP-compliant studies in a world-class facility. Ideal for passionate scientists committed to advancing drug discovery and development.

Group Leader – Preclinical Division

• Department: Preclinical Division
• Role: Lead bioanalytical and in-vitro studies as Study Director
• Experience: 10–15 years
• Education/Qualification: Relevant advanced degree in life sciences/pharma (implied)

Research Scientist – Preclinical Division

• Department: Preclinical Division
• Role: Conduct DART studies with team management
• Experience: 4–6 years
• Education/Qualification: Relevant degree in life sciences/pharma (implied)

Trainee Research Scientist – Preclinical Division

• Department: Preclinical Division
• Role: Entry-level support in preclinical toxicology/pharmacology studies
• Experience: Fresher
• Education/Qualification: M.Sc Zoology or M.Pharm (Pharmacology/Toxicology)

Skills/Qualifications

• Expertise in LC-MS/MS bioanalysis
• Proficiency in in-vitro studies (IVPT, Caco-2 permeability)
• Bioanalytical method development under GLP/GCP
• Proven leadership as Study Director
• Experience conducting DART studies per ICH/OECD guidelines
• Strong team management and communication skills
• Educational background in Zoology, Pharmacology, or Toxicology

Key Responsibilities

• Lead LC-MS/MS bioanalytical projects
• Conduct in-vitro permeability studies
• Develop and validate bioanalytical methods
• Serve as Study Director for GLP studies
• Execute DART studies per regulatory guidelines
• Manage preclinical research teams
• Ensure compliance with ICH/OECD standards
• Support toxicology and pharmacology research

Benefits/Perks

• Competitive salary and incentives
• Career progression in preclinical research
• Exposure to global regulatory standards
• Continuous learning and training programs
• Innovative and scientific work environment
• Opportunity to contribute to drug development

How to Apply

Interested candidates should email their updated resume.

Email: careers@vimta.com

Subject Line: PCD Hiring – [Designation] (e.g., PCD Hiring – Group Leader)

For more preclinical and pharma opportunities, visit Pharma Recruiter.

Take the next step in your scientific career — apply today!

Why You Should Join

VIMTA Labs provides a stimulating environment driven by scientific excellence and quality commitment. Employees benefit from long-term career stability, hands-on experience in advanced preclinical research, and opportunities to work on global projects.

Join a trusted CRO recognized for innovation, regulatory compliance, and impactful contributions to healthcare advancements.

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