Job Description: Bioanalyst II
Work with some supervision, and apply established knowledge of laboratory techniques such as HPLC, dissolution, moisture by KF, GC, TLC, and others to perform pharmaceutical product stability testing.
Responsible for understanding and performing routine analytical testing for stability samples, evaluating and documenting results in a timely manner.
Understand and follow all SOPs and written test procedures.
Perform testing within established standard test times and maintains quality and productivity at acceptable levels as communicated by the supervisor.
Execute troubleshooting of instrumentation and will be expected to maintain laboratory equipment in good working condition.
Perform laboratory investigation steps with appropriate approvals and with guidance from supervisor.
Understand the investigation process and begin to assist in preparation of laboratory investigation documents.
Keep supervisor fully informed of all results and project status on a daily basis and reports critical information in a timely manner.
Perform other tasks as assigned by the supervisor (e.g. assist other colleagues with laboratory investigations, training of other analysts as assigned.
3-5 years' relevant experience with Bachelor's Degree - Chemistry, 5+ years' with Associate's Degree.
Good working knowledge of dissolution and chromatographic techniques, especially HPLC, is necessary and a requirement.
Working knowledge of both computer and/or data handling acquisition systems is necessary and required.
cGMP experience is required.
Previous pharmaceutical, quality control / stability experience preferred.