Remotely
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Job Description
📋 Description
- Review GMP laboratory data and documentation to ensure compliance with established procedures, data
- Verify logbook and documentation entries for accuracy, completeness, and adherence to GDP standards.
- Confirm the sample chain of custody throughout the testing lifecycle.
- Review audit trails to ensure actions align with procedural requirements and timelines.
- May be required to participate in cross-training opportunities across laboratory testing functions
- Develop and maintain proficiency in applicable analytical testing techniques and laboratory
🎯 Requirements
- Bachelor's degree in Chemistry, Life Sciences, or a related scientific field.
- 2+ years of cGMP experience in a regulated laboratory environment.
- Direct experience reviewing GMP data in an industrial setting.
- Hands-on experience with HPLC/UPLC and UV-Vis spectrophotometry.
- Experience with ELISA, MCE, and/or iCIEF preferred.
- Proven ability to process and review quantitative liquid chromatography data.
🎁 Benefits
- Comprehensive medical insurance options
- Full dental and vision coverage available
- Employer-sponsored life and disability insurance
- 401(k) plan with company match
- Vacation days, paid holidays, and additional PTO options
- Hourly compensation: $26.25 - $30.00 per hour
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