Are you a seasoned Microbiology professional with a passion for quality and leadership? Autocal Solutions Pvt Ltd is looking for an experienced Technical Manager - Microbiology to join their team. Details are Provided below 1. Key Requirements: -Minimum of 8+ years of experience in a testing laboratory environment. -Proven background in testing related to Food, Air, and Water. -The ideal candidate will have strong technical expertise, a deep understanding of laboratory operations, and the ability to lead and mentor a team to ensure the highest standards of quality and accuracy. Qualifications : A Master's Degree in Microbiology Minimum- Exp. 8 Years Excellent communication and collaboration skills. Ability to multitask and work on multiple projects simultaneously. Ability to work in a fast-paced environment and meet tight deadlines. If you have a knack for problem-solving and a commitment to excellence, company want to hear from you! Join ...
Required Senior Toxicologist- M.sc/Ph.D. in Toxicology, Pharmacology, or related life sciences field
VIPRAGEN BIOSCIENCES PVT LIMITED IS HIRING FOR SENIOR TOXICOLOGIST
About Vipragen Biosciences Pvt. Ltd : Vipragen Biosciences Pvt ltd is a leading organization specializing in drug discovery and development services. They are committed to advancing scientific research and innovation through cutting-edge technology and a collaborative work environment. At present company is looking for Senior Toxicologist
Details are Provided below
1. Position: Senior Taxicologist
2. Location: Mysore, Karnataka
3. Experience: 8-15 years
4. Industry: Preclinical CRO (GLP-OECD certified)
5. About the Role:
Vipragen Bioscience Pvt Ltd is seeking an experienced and highly skilled Toxicologist to join their growing team at OECD GLP-certified preclinical CRO in Mysore. The ideal candidate will be responsible for conducting and overseeing in vivo repeated dose toxicity studies for global regulatory submissions. Candidates with a DABT certification will be preferred.
6. Key Responsibilities:
-Independently design, conduct, and interpret in vivo repeated dose toxicity studies for regulatory submissions across the globe (FDA, OECD, EU, REACH, etc.)
-Select appropriate doses and determine PODs (NOEL, NOAEL, STD10) based on preclinical toxicology
results
-Ensure all preclinical research and reports comply with GLP, OECD, ICH, Indian Schedule Y, and other global regulatory guidelines
-Contribute to pre-clinical/non-clinical development plans, including study design, data interpretation, and strategy support for pharmaceuticals, agrochemicals, biotechnology products, and medical devices.
-Provide risk assessment and regulatory support to ongoing R&D projects
-Lead and mentor a team of 5-10 toxicology professionals, providing guidance and support throughout the study lifecycle
-Resolve study-related, regulatory, and client-related issues in a timely and compliant manner
-Collaborate effectively with cross-functional teams including Sponsors/Clients, Business Development,
-Project Management, and Technical Teams
-Participate in on-site and telecon meetings to support client interactions and study updates
7. Preferred Qualifications:
M.sc/Ph.D. in Toxicology, Pharmacology, or related life sciences field
DABT Certification (preferred)
Proven expertise in preclinical toxicology, risk assessment, and regulatory submissions
Strong knowledge of GLP, OECD, FDA, EU, REACH, and IND requirements
Excellent communication, leadership, and problem-solving skills
Willingness to relocate to Mysore
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