Title: Analytical Associate (QC Chemist)

Location: North Chicago, IL

Duration: 12+ Months

Must Have:

• Experience/background in analytical sciences, e.g., sample preparation, liquid chromatography developing and validating various methods (Wet, GC, HPLC, GC-MS, LC-MS).
• Familiarity with Chromeleon CDS.
• Understanding client requirements to meet method validation criteria is a must.
• Ability to record data in notebooks according to the client criteria.
• Ability to flow to work to meet business and team timelines.
• Gas Chromatography Titration/Wet Chemistry USP Raw Material Methods (Various).
• ICP Analyst.

Job Description:

• The Analytical Chemist Associate performs physical, chemical or bioanalytical characterization of finished product or raw material test samples.
• Associate applies various chemistry techniques and scientific methods to characterize test materials to enable experimental objectives.
• Technical deliverables include but are not limited to: basic bench chemistry techniques (including pH, viscosity and particle size), sample preparation, chromatography, gravimetric analysis).
• Receives and follows instructions on assignment objectives with accuracy and great attention to detail. Spends the largest percentage of time in the laboratory.
• Associate analysts must use their analytical skills to understand how the collected data can affect business decisions, then prepare reports that detail findings and recommend solutions.
• Instrumentation operation, sample analysis, Notebook documentation, reviewing reports, quality systems compliance.
• Bachelor’s Degree in Chemistry or related field. Relevant experience in an academic or industrial lab setting with emphasis on notebook documentation.
• Ability to analyze and document various different types of data. Ability to operate basic lab equipment including pH meters, pipettes, spectrophotometer, etc. Strong math skills, attention to detail and ability to work in a fast-paced environment.

Project Description:

• We are seeking a degreed QC Chemist to support our organization in routine QC Laboratory testing. The contractor will be responsible for executing lab tests, reporting OOS and entering results in the QC Laboratory systems.
• Laboratory Testing: Perform a wide range of laboratory tests and analyses following established protocols and procedures. This includes but is not limited to raw material testing, in-process testing, finished product testing, stability testing, and environmental monitoring.
• Instrumentation and Equipment: Operate and maintain laboratory instruments and equipment necessary for testing, such as HPLC, GC, UV-Vis spectrophotometers, titration equipment, pH meters, and other relevant analytical instruments. Ensure instruments are calibrated and maintained according to established schedules.
• Method Development and Validation: Support method development and validation activities for new or modified test methods. Collaborate with the technical team to optimize and validate analytical methods for accuracy, precision, specificity, and sensitivity.
• Sample Preparation: Prepare samples for testing, which may involve weighing, diluting, extracting, or other sample preparation techniques. Adhere to proper sample handling and storage procedures to maintain sample integrity.
• Data Analysis and Reporting: Analyze test results, interpret data, and generate accurate and concise reports for review. Ensure that all results and observations are accurately documented and recorded according to established procedures.
• Quality Control and Assurance: Adhere to quality control procedures to ensure accuracy and reliability of test results. Participate in quality assurance activities, including proficiency testing, inter-laboratory comparisons, and equipment qualification.
• Compliance and Documentation: Follow Good Laboratory Practices (GLP) and applicable regulatory requirements to maintain compliance. Document all laboratory activities, including test methods, standard operating procedures (SOPs), deviations, and any changes made during testing.
• Troubleshooting and Problem Solving: Identify and resolve technical issues or challenges encountered during testing. Collaborate with cross-functional teams to investigate and troubleshoot any out-of-specification or non-conforming test results.
• Health and Safety: Comply with all laboratory safety protocols and procedures, including proper handling and disposal of hazardous materials. Adhere to personal protective equipment (PPE) requirements and maintain a safe working environment.
• Training and Development: Stay updated with relevant industry standards, regulations, and advances in analytical techniques. Engage in continuous learning and professional development to enhance technical knowledge and skills.
• Collaboration and Communication: Work collaboratively with internal stakeholders, including the Quality Control team, R&D, and Manufacturing, to support overall quality objectives. Communicate effectively to provide project updates, discuss testing requirements, and address any issues or concerns.
• Documentation Review: Participate in the review of laboratory documentation, including test records, protocols, and reports, to ensure accuracy, completeness, and compliance with applicable standards and procedures.
• Project Management: Manage workload and prioritize tasks to meet project deadlines and deliverables. Provide regular progress updates to the project lead or supervisor and escalate any issues or challenges as necessary.
• Confidentiality and Intellectual Property: Maintain strict confidentiality of all proprietary information, trade secrets, and intellectual property encountered during the engagement. Adhere to any non-disclosure agreements or confidentiality requirements.