Overview
On Site
Accepts corp to corp applications
Contract - W2
Contract - to 01/01/2027
Skills
Profit And Loss
Research
Innovation
Agile
Manufacturing
Research and Development
Supervision
Assays
Data Integrity
Regulatory Compliance
Collaboration
Product Support
HPLC
SOP
Good Manufacturing Practice
SAFE
Organized
Equipment Maintenance
Chemistry
Science
Biology
Analytical Chemistry
Instrumentation
UV
Theory Of Constraints
TOC
Conflict Resolution
Problem Solving
Communication
Analytical Skill
Attention To Detail
Pharmaceutics
GMP
Technical Writing
Testing
Job Details
Description:
12 months contract; May extend
Onsite
Location Round Lake IL
Your role at client:
The research we do and the products we develop improve outcomes for patients around the world. As an Associate Scientist I at client, 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 client, you'll use your analytical approach to identify risks and opportunities for innovation. Agile and willing to take action, you stay calm under pressure!
What you'll be doing:
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 client SOP's and policies on cGMP's 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.
What you'll bring:
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
This work is subject to hazards including exposure to chemicals and drug products. Penicillin and Cephalosporin containing products and/or materials may be present in the laboratory.
Your role at client:
The research we do and the products we develop improve outcomes for patients around the world. As an Associate Scientist I at client, 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 client, you'll use your analytical approach to identify risks and opportunities for innovation. Agile and willing to take action, you stay calm under pressure!
What you'll be doing:
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 client SOP's and policies on cGMP's 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.
What you'll bring:
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
This work is subject to hazards including exposure to chemicals and drug products. Penicillin and Cephalosporin containing products and/or materials may be present in the laboratory.
Employers have access to artificial intelligence language tools (“AI”) that help generate and enhance job descriptions and AI may have been used to create this description. The position description has been reviewed for accuracy and Dice believes it to correctly reflect the job opportunity.