In Vivo Pharma Laboratory Manager - Toxikon corporation

Location: Bedford , MA
Categories: Scientist
Website: www.toxikon.com

Position Description

Candidate should have a Bachelor Degree and at least 3-5 years of managerial experience. Should have experience conducting testing of routine and non-routine In Vivo Pharma studies. Responsible for all technical aspects of In Vivo tests. Support In Vivo Toxicology studies leading to product registration (FIFRA, TSCA, FDA, ISO,ICH,OECD, and others). Investigate and conduct programs according to GLP, GMA and Non-GLP guidelines. Research and develop new test procedures and associated validations and services for the InVivo Pharma Department. Pursue and implement alternative testing programs, including lab alternatives. Responsible for the accuracy and timeliness of In Vivo reports, SOP and protocol development. Assist and manage technical site visits of the department related to assigned projects and assisting QAU and Regulatory Affairs with all vendor/regulatory audits. Manage studies, maintaining and monitoring schedule of performance, flow of information and reporting of studies. Ensure that reports are reported timely and all special tests are properly handled. Manage work assignments of the lab technicians, including their work schedules, reporting schedules, technical content and annual reviews. Assist in the budgeting and financial goals for the In Vivo Pharma department in collaboration with the Associate Director and Senior Study Directors.

How to Apply

send resumes to hr@toxikon.com or www.toxikon.com/careers

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