QC Analyst - Assays, Deviations, CAPA (Max $39/hr W2)

Pharma

Associate’s Degree Microbiology, Biochemistry or Related Science Fields

• Running test samples for (but not limited to) investigations, transfers and validations.
• Reviewing assays
• Training others
• Writing- Quality Records (Deviations, CAPA, Change Control) and Test Methods
• Projects – such as method transfers, new instruments, method qualifications
• Use of Microsoft Suites (Word, Excel, PowerPoint)
• Use of Laboratory computer systems
• Potential previous use of GMP Quality Systems such as: TrackWise, LIMS
• Works on assignments that are semi-routine in nature where ability to recognize deviation from accepted practice is required.
• Works on problems of moderate scope in which analysis of situation or data requires a review of identifiable factors.

• Applies job skills and company's policies and procedures to complete a variety of tasks.
• Running test samples for In-Process, Lot Release and Stability studies.
• Apply Data Integrity principles in all aspects of work, in compliance with *** DI policies, guidelines and procedures.
• Perform other duties as assigned.

All your information will be kept confidential according to EEO guidelines.