Chemist
Job Title: Chemist
Location: Los Angeles, CA
Duration: 06+ Months
Duties And Responsibilities
Location: Los Angeles, CA
Duration: 06+ Months
Duties And Responsibilities
- Generate, review and execute phrase appropriate method validation/verification/transfer protocols
- Translate technical information and requirements into experimental design
- Prepare documentation in support of the sampling, analysis, and reporting of method validation results
- Perform troubleshooting during method validation and transfer
- Perform data analysis, interpretation and review using statistical methods
- Prepare summaries and reports
- Author, compile and track deviations or issues encountered during analytical method validations or transfers
- Write, review and assist in the evaluation of the effectiveness of SOPs and identify necessary changes following validation activities. Ensure that SOPs are current
- Assist in the maintenance of validation/verification/transfer documents
- Assist in writing risk analysis (or statistical analysis) as part of validation activities
- Monitor and track of validation/verification/transfer activities
- Investigate deviations in validation protocols, identify the root cause of the deviation, issue corrective and preventive actions, and carry out follow-up once the actions are implemented to ensure their effectiveness
- BS or MS in Analytical Chemistry or equivalent
- 3+ years’ experience in a cGMP pharmaceutical/biotechnology laboratory
- Strong technical knowledge KF titrators, HPLC, and protein analysis (Coomassie Stain, Western Blots), etc.
- Strong working knowledge of analytical instruments/software and analytical validation and method transfer principles
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Seniority level
Mid-Senior level -
Employment type
Contract -
Job function
Research, Analyst, and Information Technology -
Industries
Staffing and Recruiting
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