Job Description
**Job Description Summary**
Professional Summary
Candidate must have Experienced and detail-oriented Senior Analyst with over 10 years in Quality Control within the pharmaceutical and chemical industries.
Proven expertise in analytical instrumentation including HPLC, GC, and LCMS, method development and validation, and regulatory compliance. Adept at troubleshooting, data interpretation, and ensuring product quality in alignment with GMP standards.
________________________________________
Core Competencies
• High-Performance Liquid Chromatography (HPLC)
• Gas Chromatography (GC)
• Liquid Chromatography–Mass Spectrometry (LCMS)
• Analytical Method Development & Validation
• Stability Studies & Impurity Profiling
• GMP, GLP & Regulatory Compliance
• Instrument Calibration & Maintenance
• Data Analysis & Documentation (LIMS, Empower, Chromeleon)
• Team Collaboration & Training
________________________________________
Professional Experience
Senior Analyst – Quality Control
Lead analytical testing using HPLC, GC, and LCMS for raw materials, intermediates, and finished products.
• Develop and validate analytical methods in compliance with ICH guidelines.
• Perform routine and non-routine analysis, stability studies, and impurity profiling.
• Maintain and calibrate analytical instruments ensuring minimal downtime.
• Prepare and review technical documents including SOPs, STPs, and validation protocols.
• Collaborate with cross-functional teams for investigations and CAPA implementation.
• Train junior analysts on instrument handling and analytical techniques.
• Conducted routine QC testing using HPLC and GC.
• Supported method transfer and troubleshooting activities.
• Ensured compliance with GMP and maintained accurate documentation.
• Participated in internal audits and regulatory inspections
**Job Description**
**Professional Summary**
Candidate must have Experienced and detail-oriented Senior Analyst with over 10 years in Quality Control within the pharmaceutical and chemical industries.
Proven expertise in analytical instrumentation including **HPLC, GC, and LCMS** , method development and validation, and regulatory compliance. Adept at troubleshooting, data interpretation, and ensuring product quality in alignment with GMP standards.
**Core Competencies**
+ High-Performance Liquid Chromatography (HPLC)
+ Gas Chromatography (GC)
+ Liquid Chromatography–Mass Spectrometry (LCMS)
+ Analytical Method Development & Validation
+ Stability Studies & Impurity Profiling
+ GMP, GLP & Regulatory Compliance
+ Instrument Calibration & Maintenance
+ Data Analysis & Documentation (LIMS, Empower, Chromeleon)
+ Team Collaboration & Training
**Professional Experience**
**Senior Analyst – Quality Control**
Lead analytical testing using HPLC, GC, and LCMS for raw materials, intermediates, and finished products.
+ Develop and validate analytical methods in compliance with ICH guidelines.
+ Perform routine and non-routine analysis, stability studies, and impurity profiling.
+ Maintain and calibrate analytical instruments ensuring minimal downtime.
+ Prepare and review technical documents including SOPs, STPs, and validation protocols.
+ Collaborate with cross-functional teams for investigations and CAPA implementation.
+ Train junior analysts on instrument handling and analytical techniques.
+ Conducted routine QC testing using HPLC and GC.
+ Supported method transfer and troubleshooting activities.
+ Ensured compliance with GMP and maintained accurate documentation.
+ Participated in internal audits and regulatory inspections
All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, or status as a protected veteran.
Professional Summary
Candidate must have Experienced and detail-oriented Senior Analyst with over 10 years in Quality Control within the pharmaceutical and chemical industries.
Proven expertise in analytical instrumentation including HPLC, GC, and LCMS, method development and validation, and regulatory compliance. Adept at troubleshooting, data interpretation, and ensuring product quality in alignment with GMP standards.
________________________________________
Core Competencies
• High-Performance Liquid Chromatography (HPLC)
• Gas Chromatography (GC)
• Liquid Chromatography–Mass Spectrometry (LCMS)
• Analytical Method Development & Validation
• Stability Studies & Impurity Profiling
• GMP, GLP & Regulatory Compliance
• Instrument Calibration & Maintenance
• Data Analysis & Documentation (LIMS, Empower, Chromeleon)
• Team Collaboration & Training
________________________________________
Professional Experience
Senior Analyst – Quality Control
Lead analytical testing using HPLC, GC, and LCMS for raw materials, intermediates, and finished products.
• Develop and validate analytical methods in compliance with ICH guidelines.
• Perform routine and non-routine analysis, stability studies, and impurity profiling.
• Maintain and calibrate analytical instruments ensuring minimal downtime.
• Prepare and review technical documents including SOPs, STPs, and validation protocols.
• Collaborate with cross-functional teams for investigations and CAPA implementation.
• Train junior analysts on instrument handling and analytical techniques.
• Conducted routine QC testing using HPLC and GC.
• Supported method transfer and troubleshooting activities.
• Ensured compliance with GMP and maintained accurate documentation.
• Participated in internal audits and regulatory inspections
**Job Description**
**Professional Summary**
Candidate must have Experienced and detail-oriented Senior Analyst with over 10 years in Quality Control within the pharmaceutical and chemical industries.
Proven expertise in analytical instrumentation including **HPLC, GC, and LCMS** , method development and validation, and regulatory compliance. Adept at troubleshooting, data interpretation, and ensuring product quality in alignment with GMP standards.
**Core Competencies**
+ High-Performance Liquid Chromatography (HPLC)
+ Gas Chromatography (GC)
+ Liquid Chromatography–Mass Spectrometry (LCMS)
+ Analytical Method Development & Validation
+ Stability Studies & Impurity Profiling
+ GMP, GLP & Regulatory Compliance
+ Instrument Calibration & Maintenance
+ Data Analysis & Documentation (LIMS, Empower, Chromeleon)
+ Team Collaboration & Training
**Professional Experience**
**Senior Analyst – Quality Control**
Lead analytical testing using HPLC, GC, and LCMS for raw materials, intermediates, and finished products.
+ Develop and validate analytical methods in compliance with ICH guidelines.
+ Perform routine and non-routine analysis, stability studies, and impurity profiling.
+ Maintain and calibrate analytical instruments ensuring minimal downtime.
+ Prepare and review technical documents including SOPs, STPs, and validation protocols.
+ Collaborate with cross-functional teams for investigations and CAPA implementation.
+ Train junior analysts on instrument handling and analytical techniques.
+ Conducted routine QC testing using HPLC and GC.
+ Supported method transfer and troubleshooting activities.
+ Ensured compliance with GMP and maintained accurate documentation.
+ Participated in internal audits and regulatory inspections
All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, or status as a protected veteran.
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