Quality Control Analyst II, Release & Stability Testing (3rd Shift - Contract)

Duties And Responsibilities

• Perform analytical testing using HPLC/UPLC/cGE/icIEF instruments following GMP documents
• Create/revise SOPs, Protocols and Reports
• Practice safe work habits and adhere to safety procedures and guidelines
• Perform maintenance and cleaning of laboratory equipment
• SME to support or lead activities related to OOS/OOT investigations, deviations, change controls, corrective actions, and preventive actions to correct and eliminate the potential for non-conformances
• Update and track metrics for trending and reporting; stability and QC analytical data
• Task and team-oriented, analytical, organized, detail-oriented, self-motivated and ability to multitask

Qualifications

• Bachelor's Degree in Life Sciences discipline
• Minimum 3+ years’ experience in a cGMP analytical lab environment
• Must have the ability and skill to perform the detailed job requirements competently, safely, accurately, and proficiently
• Self-starting motivated person who possesses excellent time management, the ability to adapt to change and organizational skills
• Able to communicate, receive, and understand information and ideas with diverse groups of people in a collaborative, comprehensible and reasonable manner
• Able to use and learn standard office equipment and technology with proficiency
• Experience in Empower chromatography software