- Conduct and support GLP-compliant biocompatibility and toxicity studies.
- Work as Study Personnel (SP) or Study Director (SD) for assigned studies.
- Prepare and review study plans, protocols, and study reports.
- Ensure compliance with OECD GLP, ISO 10993, and CCSEA guidelines.
- Maintain study documentation and coordinate with QAU, veterinarians, and sponsors.
Qualification & Experience
- Qualification: M.V.Sc./M.Pharm./M.Sc. in Toxicology, Pharmacology, Veterinary Sciences, or related Life Sciences.
- Experience: Minimum 01 - 02 years of experience in the relevant field.
- Domain Expertise GLP Experience is Preferable. Knowledge of ISO 10993 biocompatibility and toxicity studies, Good scientific writing and communication skills.
- Computer literacy includes advanced proficiency with Microsoft Office (Excel,
word and
PPT).
- Excellent communication and presentation skills, analytical, problem-solving skills and interpersonal abilities, decision making, excellent oral and written communication skills in English.
- Must have team spirit, agility, leadership, initiative, time management, prioritizing and the ability to handle a complex and wide-ranging workload.
- Must maintain confidentiality and discretion in all aspects and be comfortable with aflexible working schedule to meet the needs of the Company.
- Ability to handle urgent matters, multiple tasks simultaneously and quickly complete the assigned tasks.
- Willingnessto travel
📌 Veterinary Doctor (Visakhapatnam)
🏢 Kalam Institute Of Health Technology
📍 Visakhapatnam
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