QC Analytical Associate

Job Title: QC Analytical Associate

Location: North Chicago, IL, 60064

Duration: 11 Months

Job 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.

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 of client requirements to meet method validation criteria is a must
• Ability to record data in notebooks according to client criteria
• Ability to flow to the work to meet business and team timelines
• Gas Chromatography Titration/Wet Chemistry USP Raw Material Methods (Various)
• ICP Analyst

Nice To Have:
• Communication
• Excellent communication and coordination skills
• An analytical mindset
• Proactive problem-solving skills and attention to detail
• Analytical Laboratory