Biotechnician: Maintains production records, and physical inventory; maintains in-process checks and assists in developmental work pertaining to production methods when required. Documents all work according to proper cGMP documentation practices and performs review of manufacturing documentation. Performs all work duties via automated systems or manual operations in compliance with safe operating procedures, company and government regulations, and good manufacturing practices. Cleans, assembles, operates, disassembles, maintains and trouble shoots as required to meet production schedules. Dispose of Process waste material as per departmental SOP and regulatory guidelines. Upon reaching Biotechnician Level 2 additional responsibilities have included: input into the creation of a regimented training program including the design of a performance statistics worksheet in Microsoft Excel, working with management to improve areas of routine problems, involvement in streamlining production areas, assisting in updates to SOPs and SMFs with changes to ensure ease of use.

Lead technician for complex in-life studies with minimal supervision from management. Responsibilities included overseeing technicians working on studies and reviewing data obtained on daily and weekly basis. Responsible for compiling necessary equipment and supplies through warehouse storage and overseeing procurement of supplies not kept in stock. Ensured quality data entry with Good Laboratory Practices guidelines and ensured technicians on studies adhered to protocols and SOPs. Responsibilities included addressing deviations from protocol and presentation of statistical data to supervisors and study directors for determining study impact.

Lead technician for multiple basic and complex in-life studies with moderate supervision from management. Work responsibilities include measurement and statistical data collection by guidelines compliant with Good Laboratory Practices. Responsibilities included working with supervisors to compile and generate necessary record keeping materials for duration of studies. Other responsibilities included presentation of statistical data to supervisors, and study directors for assessment of study objectives and evaluation of measured and projected outcomes. As lead technician on studies I served as a mentor to new staff for laboratory procedures and protocols.

Generation and record keeping of data in the compliance with Good Laboratory Practice Regulations and Standard Operating Procedures. Responsible for handling and restraining animals, clinical observations, sample collection, monitoring food consumption, animal husbandry, and performing accurate data collection and reporting. Administer test substances by various basic methods Non-technical responsibilities included observation and assessment of study animals for general health.