Vivo Bio Tech Ltd, a leading GLP-certified Preclinical Contract Research Organization (CRO), is hiring experienced professionals across multiple departments. This is an excellent opportunity for candidates with strong exposure to analytical chemistry, ADME studies, quality assurance, and business development to join a reputed CRO known for regulatory compliance and global research standards.
Open Positions & Requirements
1️⃣ Study Director – Analytical Chemistry
Department: Analytical Chemistry
Qualification: MSc Life Sciences / M.Pharm
Experience: 3 – 7 years
Key Skills:
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GLP analytical studies
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Method validation & data review
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Regulatory documentation
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CRO study management experience
2️⃣ Study Director – ADME
Department: ADME
Qualification: MSc Life Sciences / M.Pharm
Experience: 3 – 7 years
Key Skills:
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ADME study design & execution
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Pharmacokinetics & bioanalysis
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GLP compliance & regulatory submissions
3️⃣ Quality Auditor
Department: Quality Assurance
Qualification: MSc Life Sciences / M.Pharm
Experience: 3 – 5 years
Key Skills:
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GLP audits & inspections
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SOP review & compliance
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Internal & external audit handling
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CRO quality systems
4️⃣ Business Development Executive (BDE)
Department: Business Development
Qualification: MSc Life Sciences / M.Pharm / MBA
Experience: 1 – 2 years
Key Skills:
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CRO business development
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Client coordination & proposals
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Scientific sales & marketing exposure
Eligibility Criteria
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Relevant experience in GLP-certified CRO companies
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Exposure as Study Director / Study Personnel / QA / Veterinarian preferred
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Strong documentation and regulatory knowledge
