Job Description

Job Title: Quality Control Analyst-III

Duration: 6+ Months

Location: Camarillo CA 93012

Qualifications:

• - Bachelor's Degree in Chemistry or related field
• - Minimum 5 years of relevant pharmaceutical experience

Responsibilities:

• - Perform complex testing and data evaluation
• - Perform complex Liquid/Gas Chromatography, UPLC, and other testing, and, as needed, troubleshoot issues
• - Participate in or assist with test method validations
• - Evaluate data for trends
• - Support supervisors in OOS Investigations and complete CAPA requirements
• - Interact with outside departments including attending meetings, providing updates, etc.
• - Coordinate testing performed at outside testing labs, raw materials, etc.
• - Maintain a detailed and accurate recording of activities and results on paperwork
• - Execute, author, and review SOPs, reports, protocols, investigations, change controls, and data summaries. Understand and use basic risk assessment and root cause tools
• - Train upon and understand methods, equipment and standard operating procedures
• - Provide training to others as needed. Attend internal and external training on related subjects, including both intra- and inter-departmental cross-training on new techniques and procedures
• - Support equipment upkeep
• - Prepare and order supplies, as necessary
• - Enter data into relevant data management systems. Perform tracking and trending of data as requested. Compile data and provide data summaries to management
• - Utilize a thorough understanding of regulatory and compliance guidelines for the pharmaceutical industry
• - Interact with other departments within the company for testing needs and scheduling
• - May lead departmental projects with the opportunity to participate in or lead cross-functional teams, including continuous improvement projects and new customer teams
• - May lead stability program including management of test points, reporting of data, and investigations of out of specification or aberrant stability results

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