Conduct routine preparations for stability, raw materials, in-process, microbiology/ cleaning validation program and other requested testing according to Standard Operating Procedures (SOP) and Analytical Methods in accordance with current Good Manufacturing Practices (cGMPs) and regulatory requirements
Complete projects with supervision and have a clear understanding of Good Laboratory Practices (GLPs), cGMPS, and other regulatory requirements
Ability to exercise judgment and appropriately raises issues to QC management
Key focus will be preparing solutions (mobile phase, diluent, etc) and standard/sample preparations
Outstanding interpersonal skills, both written and oral, and will be encouraged to collaborate with other analysts and management
Ensures equipment is performing well and communicates and takes appropriate action as necessary
Required to follow good documentation practices
Works cross-functionally to complete projects and testing
Job Posting Qualifications
Job Posting Qualifications
Bachelor’s or equivalent
Generally, requires minimal to no prior relevant work experience
Demonstrated knowledge of analytical equipment and instrumentation and working in a GMP environment is helpful
Proven skills in coordinating and leading day to day tasks and working in collaboration to accomplish deadlines and objectives
