Kemin combines sound molecular science with the human qualities of creativity, curiosity and collaboration to improve the lives of humans and animals around the world. Using superior science, Kemin manufactures more than 500 specialty ingredients that deliver important nutrition and health benefits through products consumed by people and animals.
Job Title : Associate Scientist I - Ecotoxicology
Job ID : 2014-3144
Position Objective :
- To design,establish, maintain and up keep the Eco Toxicology Facility as per standard requirements
- To implement and perform eco toxicology practices in compliance with international/national guidelines
- Planning, performing , monitoring and maintaining of various activities
- To prepare and implement SOPs and formats required for the best practices and maintenance of the facility
Responsibilities :
- Overall responsibility for the eco toxicology program and maintenance
- Well versed with various aspects of eco toxicology program and experimentation with different species
- Complying with international/national ethics, regulations and other requirements
- Comply with international /national guidelines
- Implement and comply with GLP requirements for the facility
- Communicate with outside vendors/suppliers for purchase of materials
- To supervise and set guidelines with respect to different species used
- To ensure that all the procedures followed in eco toxicology program/facility are approved
- To ensure the highest standards of Quality and compliance are maintained in the facility and in Experimentation
- To maintain and upgrade the facility as per the standard norms
- To co-ordinate with maintenance department, stores, accounts and administration for routine activities
- To ensure appropriate training of the staffs handling different species and carrying tests for skill update and enhancement
- Budget plan for maintenance and upgradation of facility
- To Co-ordinate with the external agencies for the procurement of materials and other related aspects
- Preparation of protocols/study plan and reports for approval
Qualification : Post Graduate in life sciences with any specialization
Experience: With 2 to 6 years of working experience in a GLP certified pharma R& D or a preclinical CRO is required
Apply Below :
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