Job Title: Scientist 1, Analytical Chemistry
Rate of pay ***
On site 5 days
Segment/Department Name: Infection Prevention, Analytical Chemistry
This position provides analytical chemistry support and/or remediation to all chemistry-related projects for Client products currently on the market as well as new product development. This position will also participate in the conduct of the stability testing program to support the approval of process and/or product design changes. As needed, this position also supports the development and validation of analytical methodologies for incoming raw materials, in-process, and finished product release testing.
Chemistry & performance testing, data review and entry, protocol/report generation, laboratory maintenance and support.
BS/MS in Chemistry / Pharmaceutics with related science experience
o Demonstrates developed knowledge of respective scientific discipline and standard scientific method and techniques.
o Excellent scientific writing skills.
o Ability to multi-task various activities.
o Troubleshoot issues that arise and solve problems.
o Ability to interpret a variety of instructions furnished in written, oral, diagram, or schedule form.
o 2-4 years experience in pharmaceutical analytical chemistry is essential.
o Hands-on experience with wet-chemistry and instrumental techniques (i.e. pH, tritration, UV-Vis, GC, HPLC).
o Experience in working within an FDA regulated environment and GMP documentation requirements.
o Ability to discuss scientific strategies/results and interact with other functional areas, including Regulatory, Manufacturing, and Quality.
o Previous experience with writing scientific protocols and reports.
Job Title: Scientist 1, Analytical Chemistry
Rate of pay ***
On site 5 days
Segment/Department Name: Infection Prevention, Analytical Chemistry
This position provides analytical chemistry support and/or remediation to all chemistry-related projects for Client products currently on the market as well as new product development. This position will also participate in the conduct of the stability testing program to support the approval of process and/or product design changes. As needed, this position also supports the development and validation of analytical methodologies for incoming raw materials, in-process, and finished product release testing.
Chemistry & performance testing, data review and entry, protocol/report generation, laboratory maintenance and support.
BS/MS in Chemistry / Pharmaceutics with related science experience
o Demonstrates developed knowledge of respective scientific discipline and standard scientific method and techniques.
o Excellent scientific writing skills.
o Ability to multi-task various activities.
o Troubleshoot issues that arise and solve problems.
o Ability to interpret a variety of instructions furnished in written, oral, diagram, or schedule form.
o 2-4 years experience in pharmaceutical analytical chemistry is essential.
o Hands-on experience with wet-chemistry and instrumental techniques (i.e. pH, tritration, UV-Vis, GC, HPLC).
o Experience in working within an FDA regulated environment and GMP documentation requirements.
o Ability to discuss scientific strategies/results and interact with other functional areas, including Regulatory, Manufacturing, and Quality.
o Previous experience with writing scientific protocols and reports.
['" Basic knowledge of quality systems regulations, ISO Quality System and Medical Device standards. " Ability to effectively communicate both verbally and in writing to all levels within the organization and external to the organization. " Ability to work in teams, including large multifunctional teams, and independently obtain results as required with minimal supervision. Proven ability to use initiative and drive to achieve results. " Excellent attention to detail with a high degree of accuracy and the ability to work independently and in team situations. " Ability to identify, analyze, develop, and present solutions for problems of moderate scope and complexity. " Ability to collect, analyze data and present results to others orally or in writing. " Must be able to comprehend and summarize data and document into reports. " Must be Self-motivated, organized and detail oriented. " Ability to handle multiple task assignments and effectively manage time and priorities to meet deadlines. " Ability to develop work plans and manage them to meet agreed upon goals. " Skilled in Microsoft software; excellent Excel data extraction and analysis skills; SAP proficiency strongly preferred; ability to learn and master other software programs'] Shift: ['" Basic knowledge of quality systems regulations, ISO Quality System and Medical Device standards. " Ability to effectively communicate both verbally and in writing to all levels within the organization and external to the organization. " Ability to work in teams, including large multifunctional teams, and independently obtain results as required with minimal supervision. Proven ability to use initiative and drive to achieve results. " Excellent attention to detail with a high degree of accuracy and the ability to work independently and in team situations. " Ability to identify, analyze, develop, and present solutions for problems of moderate scope and complexity. " Ability to collect, analyze data and present results to others orally or in writing. " Must be able to comprehend and summarize data and document into reports. " Must be Self-motivated, organized and detail oriented. " Ability to handle multiple task assignments and effectively manage time and priorities to meet deadlines. " Ability to develop work plans and manage them to meet agreed upon goals. " Skilled in Microsoft software; excellent Excel data extraction and analysis skills; SAP proficiency strongly preferred; ability to learn and master other software programs']| Location | Vernon Hills, IL |
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