What are the responsibilities and job description for the USA - Research Scientist II position at eTeam Inc.?
Research Scientist : Medication Delivery Analytical Strategies and Laboratories.
Round Lake , IL
12 Months Extendable Contract
Description
Perform analytical method development, validation, and chemical analysis associated with drug products and impurities including LC or GC with MS detection. Perform validation of analytical methods for quantitative analysis. Specifically, this position is expected to:
• Independently execute analytical testing following written test procedures and study protocols, document results per GXP regulations, and review data for accuracy and completeness.
• Apply analytical separation and detection techniques for complex impurity identification/quantification.
• Design and execute method validation and transfer studies.
• Assess the technical feasibility of complex research and design concepts.
• Contribute to the analytical problem-solving efforts to meet urgent business needs.
• Collaborate with other functions such as project management, regulatory, formulation, engineering, manufacturing, and quality control in project teams.
• Collaborate with organizations external partners to ensure successful execution of analytical testing and study designs.
• Maintain knowledge of relevant QSR and other regulatory requirements related to R&D (product development, design, and safety) to ensure compliance in all research, data collection and reporting activities.
• Develop an in-depth knowledge and understanding of cGxP and related regulations and guidance, and participate in the generation, review, adoption, and interpretation of them.
• Maintain focus on meeting both external and internal customer expectations.
Qualifications
• Bachelor’s degree in relevant scientific discipline (chemistry, pharmaceutical sciences) with 5-7 years’ experience or Masters’ degree with 3-5 years’ experience or PhD with 0-3 years’ experience.
• Proficient at GC/MS and/or LC/MS analysis.
• Experienced with analytical method development, validation,- and transfer in pharmaceutical regulated laboratories.
• A good understanding of ICH, USP guidelines and cGxP practice.
• Familiarity and hands-on experience with HPLC, GC, UV, MassHunter and other analytical instruments and software.
• Ability to learn quickly and to solve problems in a timely manner using analytical chemistry skills.
• Possess relevant writing and computer skills.
• Ability to design experiments and draw meaningful conclusions from lab data.
• Quality oriented.
• Ability to adapt to changes and to work in a team environment.
Round Lake , IL
12 Months Extendable Contract
Description
Perform analytical method development, validation, and chemical analysis associated with drug products and impurities including LC or GC with MS detection. Perform validation of analytical methods for quantitative analysis. Specifically, this position is expected to:
• Independently execute analytical testing following written test procedures and study protocols, document results per GXP regulations, and review data for accuracy and completeness.
• Apply analytical separation and detection techniques for complex impurity identification/quantification.
• Design and execute method validation and transfer studies.
• Assess the technical feasibility of complex research and design concepts.
• Contribute to the analytical problem-solving efforts to meet urgent business needs.
• Collaborate with other functions such as project management, regulatory, formulation, engineering, manufacturing, and quality control in project teams.
• Collaborate with organizations external partners to ensure successful execution of analytical testing and study designs.
• Maintain knowledge of relevant QSR and other regulatory requirements related to R&D (product development, design, and safety) to ensure compliance in all research, data collection and reporting activities.
• Develop an in-depth knowledge and understanding of cGxP and related regulations and guidance, and participate in the generation, review, adoption, and interpretation of them.
• Maintain focus on meeting both external and internal customer expectations.
Qualifications
• Bachelor’s degree in relevant scientific discipline (chemistry, pharmaceutical sciences) with 5-7 years’ experience or Masters’ degree with 3-5 years’ experience or PhD with 0-3 years’ experience.
• Proficient at GC/MS and/or LC/MS analysis.
• Experienced with analytical method development, validation,- and transfer in pharmaceutical regulated laboratories.
• A good understanding of ICH, USP guidelines and cGxP practice.
• Familiarity and hands-on experience with HPLC, GC, UV, MassHunter and other analytical instruments and software.
• Ability to learn quickly and to solve problems in a timely manner using analytical chemistry skills.
• Possess relevant writing and computer skills.
• Ability to design experiments and draw meaningful conclusions from lab data.
• Quality oriented.
• Ability to adapt to changes and to work in a team environment.
USA - Project Manager Scientific II
Cube Hub Inc. -
Round Lake, IL
Scientist II (Bioanalytical)
US Tech Solutions -
North Chicago, IL
Research Associate Scientific II
KYYBA, Inc -
Round Lake, IL
