QC Analyst, 2nd Shift Representative
Core
Conduct routine and non-routine analysis of in-process samples, raw materials, and other requested testing to support in-process testing per SOPs and Analytical Methods in accordance with cGMPs and regulatory requirements.
Role type
Quality Control Analyst
Builds
Nucleic acid therapeutics for life-changing, lifesaving medicines
Domain
Biopharma / Analytical Chemistry
Required skills
HPLC, UV, wet chemistry, data review for compliance, troubleshooting abnormalities, equipment maintenance, Good Laboratory Practices (GLPs), Good Manufacturing Practices (cGMPs), Standard Operating Procedures (SOPs)
Preferred skills
None stated
Technologies
HPLC, UV
Responsibilities
Conduct analysis on in-process samples, raw materials, and other requested testing; Review data for compliance to specifications and troubleshoot abnormalities; Ensure equipment is performing well and take appropriate action; Follow good documentation practices; Exercise judgment in selecting methods and techniques for obtaining results
Seniority
Mid-level, hands-on IC
