Randstad USA
Job Summary
The research we do and the products we develop improve outcomes for patients around the world. As an Associate Scientist I at Company, your work contributes directly to making a significant impact on others. We collaborate cross-functionally and lead by influence. As a key part of projects, our research and development team is responsible for delivering results to drive decisions and ensure safety of our existing and new products. We work on products that make a meaningful difference in others' lives. When you join Company, you'll use your analytical approach to identify risks and opportunities for innovation. Agile and willing to take action, you stay calm under pressure!
Location: Round Lake, Illinois
Job type: Contract
Salary: $25.00 - 29.60 per hour
Work hours: 9 to 5
Education: Bachelors
Responsibilities
Conduct critical chemical and physical analyses on finished product R&D stability samples. May also support testing of raw materials, initial, in-process, and final product samples from manufacturing facilities or other R&D initiatives. Work under minimum supervision.
Perform chemical assays requiring precise analytical skills and understanding of chemistry principles.
Complete all testing, including special project / protocol testing in a timely and appropriate manner to meet project schedules.
Maintain data integrity and ensure compliance with company SOPs and specifications, FDA, cGxP, and QSR regulations.
Collaborate with other functions/departments to solve problems, increase efficiency, improve quality and provide product support.
Use sophisticated laboratory instrumentation (HPLC, pH, UV, titrations, Particle, TOC, Flame photometry, etc) and computer systems to collect and record data.
Follow, understand and comply with Company SOPs and policies on cGMPs and safety. Maintain a clean, safe and organized lab area, and potentially assume responsibility to ensure that others maintain their lab areas.
Maintain laboratory safety requirements, perform equipment maintenance/calibration, and troubleshoot instrumentation.
Qualifications
Bachelors degree in relevant scientific discipline (e.g. chemistry, pharmaceutical sciences, biology) 6 months or more of experience
Analytical chemistry instrumentation experience with pH, UV, titrations, Particle, TOC is preferred but not required.
Must have experience in a regulated environment and strong technical problem-solving skills.
Must have good oral and written communication skills, strong analytical skills and be detail oriented.
Electronic Lab Notebook experience is preferred but not required.
Pharmaceutical GMP laboratory experience is desired.
Empower experience is preferred
Must be able to handle multiple tasks concurrently and in a timely fashion.
Possess relevant laboratory/technical, writing, and computer skills.
Ability to organize and communicate complex information effectively with managers and peers
This is an on-site position.
Physical Activities and Requirements
Must be able to hand write and use computers for the majority of the work day
Must be able to transfer materials, mix solutions/product(s), open products, and perform laboratory testing
May require standing for extended periods
Must be able to lift up to 10 pounds routinely
Must not be color blind
Skills
SOP, GCP (Good Clinical Practice), GMP (Good Manufacturing Practice), High Pressure Liquid Chromatography (HPLC), Good Laboratory Practices (GLP), Food and Drug Administration (FDA)
Equal Opportunity Employer Race, Color, Religion, Sex, Sexual Orientation, Gender Identity, National Origin, Age, Genetic Information, Disability, Protected Veteran Status, or any other legally protected group status.
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Location: Round Lake, Illinois
Job type: Contract
Salary: $25.00 - 29.60 per hour
Work hours: 9 to 5
Education: Bachelors
Responsibilities
Conduct critical chemical and physical analyses on finished product R&D stability samples. May also support testing of raw materials, initial, in-process, and final product samples from manufacturing facilities or other R&D initiatives. Work under minimum supervision.
Perform chemical assays requiring precise analytical skills and understanding of chemistry principles.
Complete all testing, including special project / protocol testing in a timely and appropriate manner to meet project schedules.
Maintain data integrity and ensure compliance with company SOPs and specifications, FDA, cGxP, and QSR regulations.
Collaborate with other functions/departments to solve problems, increase efficiency, improve quality and provide product support.
Use sophisticated laboratory instrumentation (HPLC, pH, UV, titrations, Particle, TOC, Flame photometry, etc) and computer systems to collect and record data.
Follow, understand and comply with Company SOPs and policies on cGMPs and safety. Maintain a clean, safe and organized lab area, and potentially assume responsibility to ensure that others maintain their lab areas.
Maintain laboratory safety requirements, perform equipment maintenance/calibration, and troubleshoot instrumentation.
Qualifications
Bachelors degree in relevant scientific discipline (e.g. chemistry, pharmaceutical sciences, biology) 6 months or more of experience
Analytical chemistry instrumentation experience with pH, UV, titrations, Particle, TOC is preferred but not required.
Must have experience in a regulated environment and strong technical problem-solving skills.
Must have good oral and written communication skills, strong analytical skills and be detail oriented.
Electronic Lab Notebook experience is preferred but not required.
Pharmaceutical GMP laboratory experience is desired.
Empower experience is preferred
Must be able to handle multiple tasks concurrently and in a timely fashion.
Possess relevant laboratory/technical, writing, and computer skills.
Ability to organize and communicate complex information effectively with managers and peers
This is an on-site position.
Physical Activities and Requirements
Must be able to hand write and use computers for the majority of the work day
Must be able to transfer materials, mix solutions/product(s), open products, and perform laboratory testing
May require standing for extended periods
Must be able to lift up to 10 pounds routinely
Must not be color blind
Skills
SOP, GCP (Good Clinical Practice), GMP (Good Manufacturing Practice), High Pressure Liquid Chromatography (HPLC), Good Laboratory Practices (GLP), Food and Drug Administration (FDA)
Equal Opportunity Employer Race, Color, Religion, Sex, Sexual Orientation, Gender Identity, National Origin, Age, Genetic Information, Disability, Protected Veteran Status, or any other legally protected group status.
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