Weil Group, Inc
Position Overview
Our Medical Device client is seeking an experienced Laboratory Chemist for a contingent position at our Dorado facility. This is for a skilled professional to support our analytical chemistry operations.
Required Qualifications
Bachelor of Science in Chemistry** (Required)
3-5 years of professional laboratory experience** in analytical chemistry
Licenses & Certifications
Puerto Rico Chemist License** (Highly Preferred)
Technical Skills
knowledge Laboratory Equipment Proficiency
High-Performance Liquid Chromatography (**HPLC**)
Ultraviolet-Visible Spectroscopy (**UV/UV-Vis**)
Infrared Spectroscopy (**IR/FTIR**)
Other analytical instrumentation as required
Technical Knowledge
Chromatography techniques** with expertise in Empower software system
United States Pharmacopeia (USP) standards and methods
European Pharmacopoeia (EP) standards and methods
GMP/GLP laboratory practices
Method validation and qualification
Data analysis and reporting
Key Responsibilities
Perform analytical testing using HPLC, UV, IR, and other instrumentation
Execute test methods in accordance with USP, EP, and internal specifications
Operate and maintain Empower chromatography data system
Document results and maintain accurate laboratory records
Follow GMP/GLP requirements and quality standards
Support method validation and transfer activities
Troubleshoot analytical issues and contribute to investigations
#J-18808-Ljbffr
Required Qualifications
Bachelor of Science in Chemistry** (Required)
3-5 years of professional laboratory experience** in analytical chemistry
Licenses & Certifications
Puerto Rico Chemist License** (Highly Preferred)
Technical Skills
knowledge Laboratory Equipment Proficiency
High-Performance Liquid Chromatography (**HPLC**)
Ultraviolet-Visible Spectroscopy (**UV/UV-Vis**)
Infrared Spectroscopy (**IR/FTIR**)
Other analytical instrumentation as required
Technical Knowledge
Chromatography techniques** with expertise in Empower software system
United States Pharmacopeia (USP) standards and methods
European Pharmacopoeia (EP) standards and methods
GMP/GLP laboratory practices
Method validation and qualification
Data analysis and reporting
Key Responsibilities
Perform analytical testing using HPLC, UV, IR, and other instrumentation
Execute test methods in accordance with USP, EP, and internal specifications
Operate and maintain Empower chromatography data system
Document results and maintain accurate laboratory records
Follow GMP/GLP requirements and quality standards
Support method validation and transfer activities
Troubleshoot analytical issues and contribute to investigations
#J-18808-Ljbffr