QC Analyst

The world's most revolutionary biopharma companies are partnering with the client Technologies to advance the next frontier of medicine. The client continues to invest in capacity and expansion of its Colorado operations. Join our team of professionals dedicated to the development and commercialization of nucleic acid therapeutics for life changing, lifesaving medicines.

• 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

• 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