Title - Study Director - Toxicology

Roles & Responsibilities:

- Plan| Perform | Record | Report | Archive the scientific tests

- Acute studies (AOT, ADT, ADI, AEI and skin sensitization)

- Repeated toxicology studies (14/28/90 day)

- Reproduction toxicology studies (Segment I, II, III)

- Teratology Studies

- Toxicokinetic Studies

- Manage all the procedures that contribute to a GLP study. Assure Scientific | Administrative | Regulatory aspects of study are controlled.

- Review and prepare draft study plan/amendment for toxicity studies.

- Review raw data for accuracy and completeness by following ALCOA+ principles.

- Superior study report writing abilities

- Coordinate and establish clear communication links with supporting departments

- Participate in the review and revision of SOP's.

- Literature support and review for research work.

- Usage, validation, calibration and maintenance of apparatus

- To be a proactive on procuring the chemicals and requirements as per the studies.

Desired Candidate Profile:-

- Minimum of Master's degree, ideally 3-5 years of experience with relevance to Toxicology.

- Proficient in English with good communication and writing skills.

- Knowledgeable pertaining to GLP principles and global regulatory guidelines.

- Efficient utilisation of time with appropriate scheduling of given tasks.

- Active involvement, work ownership and accomplishment of organisation goals.

- Professional stability is mandatory during job switch over.

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