Cube Hub Inc.
Associate Scientist (Analytical Chemistry / Drug Research)
Cube Hub Inc., Round Lake, Illinois, United States, 60073
Associate Scientist (Analytical Chemistry / Drug Research)
As an Associate Scientist I, you will conduct critical chemical and physical analyses supporting R&D and manufacturing operations. Your work ensures the safety, quality, and innovation of life‑sustaining products. This role involves hands‑on laboratory testing, operating advanced analytical instruments, cross‑functional collaboration, and maintaining compliance with regulated environments (GMP, FDA, cGxP).
Key Responsibilities
Conduct chemical and physical analyses on finished products, raw materials, and R&D stability samples.
Perform analytical assays using techniques such as HPLC, UPLC, pH, UV, titration, TOC, particle analysis, and flame photometry.
Conduct infusion and kinetic studies to support drug delivery and release research.
Operate, troubleshoot, and maintain laboratory instrumentation, including HPLC/UPLC and other chromatography systems.
Ensure compliance with GMP guidelines, laboratory safety protocols, and data integrity standards.
Document experimental results, prepare reports, and communicate findings effectively to cross‑functional teams.
Collaborate with R&D, quality, and manufacturing teams to improve processes, product quality, and operational efficiency.
Maintain an organized and safe laboratory environment in accordance with SOPs and safety policies.
Required Technical Skills
Hands‑on experience with UPLC, HPLC, and chromatography techniques (operation, troubleshooting, and maintenance).
Proficiency in Empower software for data acquisition and analysis.
Strong background in analytical chemistry.
Experience in infusion and kinetic studies related to drug delivery.
Knowledge of GMP laboratory practices and regulatory documentation requirements.
Soft Skills
Ability to work independently and manage experiments with minimal supervision.
Strong teamwork and collaboration skills within a laboratory environment.
Excellent attention to detail, organizational, and communication skills.
Preferred Qualifications
Previous experience in pharmaceutical or cardiac drug research.
Familiarity with experimental design and data analysis for drug release studies.
Experience with Electronic Lab Notebooks (ELN) is an advantage.
Education & Experience
Bachelor’s degree in chemistry, Pharmaceutical Sciences, Biology, or related discipline.
1+ years experience in a regulated (GMP) laboratory environment preferred.
Physical Requirements
Ability to perform laboratory testing and stand for extended periods.
Regularly lift up to 10 lbs.
Must not be color blind.
Work may involve potential exposure to chemicals, penicillin, and cephalosporin‑containing materials.
Senior Level Mid‑Senior level
Employment Type Full‑time
Industries Medical Practices and Pharmaceutical Manufacturing
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Key Responsibilities
Conduct chemical and physical analyses on finished products, raw materials, and R&D stability samples.
Perform analytical assays using techniques such as HPLC, UPLC, pH, UV, titration, TOC, particle analysis, and flame photometry.
Conduct infusion and kinetic studies to support drug delivery and release research.
Operate, troubleshoot, and maintain laboratory instrumentation, including HPLC/UPLC and other chromatography systems.
Ensure compliance with GMP guidelines, laboratory safety protocols, and data integrity standards.
Document experimental results, prepare reports, and communicate findings effectively to cross‑functional teams.
Collaborate with R&D, quality, and manufacturing teams to improve processes, product quality, and operational efficiency.
Maintain an organized and safe laboratory environment in accordance with SOPs and safety policies.
Required Technical Skills
Hands‑on experience with UPLC, HPLC, and chromatography techniques (operation, troubleshooting, and maintenance).
Proficiency in Empower software for data acquisition and analysis.
Strong background in analytical chemistry.
Experience in infusion and kinetic studies related to drug delivery.
Knowledge of GMP laboratory practices and regulatory documentation requirements.
Soft Skills
Ability to work independently and manage experiments with minimal supervision.
Strong teamwork and collaboration skills within a laboratory environment.
Excellent attention to detail, organizational, and communication skills.
Preferred Qualifications
Previous experience in pharmaceutical or cardiac drug research.
Familiarity with experimental design and data analysis for drug release studies.
Experience with Electronic Lab Notebooks (ELN) is an advantage.
Education & Experience
Bachelor’s degree in chemistry, Pharmaceutical Sciences, Biology, or related discipline.
1+ years experience in a regulated (GMP) laboratory environment preferred.
Physical Requirements
Ability to perform laboratory testing and stand for extended periods.
Regularly lift up to 10 lbs.
Must not be color blind.
Work may involve potential exposure to chemicals, penicillin, and cephalosporin‑containing materials.
Senior Level Mid‑Senior level
Employment Type Full‑time
Industries Medical Practices and Pharmaceutical Manufacturing
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