Applies GMP/GLP in all areas of responsibility, as appropriate
Organizes and conducts routine analyses independently and in compliance with applicable methods, protocols, SOPs and regulatory agency guidelines
Documents work and maintains study documentation and laboratory records
Independently able to use and perform basic troubleshooting of laboratory equipment and software appropriate for assigned tasks, while learning to perform routine and non-routine maintenance
Provides input and participates in project meetings
Performs peer review and QC review of data
Performs assigned workload on a daily basis and effectively completes multiple assignments.
Contributes to a cohesive team environment and maintains a positive attitude. Plans individual workload in coordination with team members.
Maintains a clean and safe laboratory work environment
Understands data generated, and history of methods.
Recognizes deviations from normal results and inform Study Director, Principal Investigator, and/or management of any problems and/or deviations that may affect the integrity of the data and participates in corrective action of problems.
Identifies problems, determines appropriate actions, and implements solutions with support or independently as appropriate.
Able to adapt to new procedures or particular needs as directed.
Able to identify critical steps in an assay.
Leads process improvement initiatives.
Completes all required training courses.
Trains and assists less experienced staff
May assist in optimizing and validating methods for a variety of matrices
Participates in client visits or calls as needed
Learns to write text for reports, methods and, or protocols
Knowledge of departmental procedures and policies
Viewed as a resource within their team
Conducts all activities in a safe and efficient manner