(HANDS ON) HPLC expertise - able to operate, process data, and report findings into electronic lab notebook. (1+ years of experience)
Good documentation practices - bonus would be GMP/QC experience (1+ years of experience)
experience with participle detection methods (1+ years of experience)
Good organizational skills - must be able to handle multiple tasks and communicate to different teams effectively and efficiently.
Day to Day Responsibilities:
Analyze samples from Drug product related studies and process the data output according to known SOPs and protocols. All data is then transcribed into a lab notebook for compliance.
To perform experiments, organize data and analyze results under minimal supervision. With minimal supervision, plans, conducts or monitors experiments, records and organizes data, analyses results, generates robust and reliable data and/or Ensures that contracted studies are conducted in compliance with the respective protocol and applicable guidelines and regulations.
Monitors or follows established experimental design and protocols and performs routine tasks and studies to obtain reproducible and reliable results with limited supervision
Plans, monitors or conducts, analyzes and records experiments, and provides interpretation of data
Effectively transfers experimental methods from literature to the lab and makes modifications as necessary
Develops and implements new protocols with moderate review
Engages coworkers in scientific discussions
Communicates data and interpretation to work group
Skilled at developing systems to ensure quality data
Skilled and/or knowledgeable in the use of standard laboratory equipment and with one or more major laboratory instruments/techniques
Effectively trouble-shoots equipment and experimental difficulties