QC Associate Scientist I Analytical Chemistry (Pharmaceutical)

25212 W. Illinois Route 120, IL, US • Posted 14 hours ago • Updated 48 minutes ago
Contract W2
Contract Corp To Corp
On-site
Fitment

Dice Job Match Score™

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Job Details

Skills

  • Preventive Maintenance
  • Project Management
  • Performance Management
  • Health Care
  • 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
  • TOC
  • Theory Of Constraints
  • Conflict Resolution
  • Problem Solving
  • Communication
  • Analytical Skill
  • Attention To Detail
  • Pharmaceutics
  • GMP
  • Technical Writing
  • Testing

Summary

1st Shift - 8AM to 5PM

Position will be onsite.

12 months contract ; May extend

This is where you save and sustain lives

We are deeply connected by our mission. No matter your role , your work makes a positive impact on people around the world. You'll feel a sense of purpose throughout the organization, as we know our work improves outcomes for millions of patients.

Client's products and therapies are found in almost every hospital worldwide, in clinics, and in the home. For over 90 years, we have pioneered significant medical innovations that transform healthcare. Together, we create a place where we are happy, successful, and inspire each other. This is where you can do your best work.

Join us at the intersection of saving and sustaining lives- where your purpose accelerates our mission.

The research we do and the products we develop improve outcomes for patients around the world. As an Associate Scientist I , 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, 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 Baxter 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.
  • Dice Id: 91082005
  • Position Id: 2026-26325
  • Posted 14 hours ago
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