Quality Control Chemist II

At Talent Splendor, a trusted partner in pharmaceutical and chemical talent acquisition, we're seeking a dedicated Quality Control Chemist II to join our team in Arlington Heights, Illinois. This full-time, on-site position offers an exciting opportunity to advance your career in a cGMP-regulated environment within GE HealthCare’s Pharmaceutical Diagnostics division—a global leader in imaging agents for radiology. If you have strong hands-on experience with HPLC, GC, and Empower software, and a passion for maintaining the highest standards of product quality and regulatory compliance, we want to hear from you. Join us to contribute to cutting-edge pharmaceutical diagnostics while enjoying competitive pay, health insurance, paid time off, and a retirement plan. As a Quality Control Chemist II, you will play a critical role in ensuring the integrity and safety of pharmaceutical products that impact patient care worldwide. This role offers excellent career development and advancement opportunities within a global healthcare leader. Key Responsibilities Conduct routine and non-routine analytical testing of raw materials, in-process samples, and finished goods using HPLC, GC, UV-Vis, FTIR, and other advanced analytical instruments. Review , interpret, and document analytical results ensuring compliance with cGMP, USP, and ICH regulatory standards. Execute chromatographic data acquisition and processing using Empower software to support product release and stability testing. Participate in method development, validation, and troubleshooting to optimize laboratory processes and enhance testing accuracy. Maintain precise laboratory documentation including electronic records, notebooks, and logbooks to support audit readiness and regulatory inspections. Lead or support investigations related to out-of-specification (OOS) results, deviations, and laboratory discrepancies to ensure timely resolution. Contribute to continuous improvement initiatives, SOP updates, and provide training to junior staff to foster a culture of quality and compliance. Adhere strictly to laboratory safety protocols and maintain an organized, compliant work environment. What We're Looking For Required: Proven analytical laboratory experience in a regulated pharmaceutical or chemical environment, preferably within cGMP settings. Strong hands-on expertise with HPLC and GC instrumentation and proficiency in Empower software. Solid understanding of cGMP, USP, and ICH guidelines and their application in quality control testing. Excellent documentation skills and attention to detail to maintain compliance and data integrity. Ability to troubleshoot analytical methods and laboratory equipment effectively. Strong communication skills and ability to work collaboratively within cross-functional teams. Preferred: Bachelor’s degree in Chemistry, Biochemistry, or related scientific discipline. Experience with method development and validation in pharmaceutical diagnostics. Familiarity with stability testing protocols and regulatory submissions. Demonstrated commitment to continuous learning and professional growth. What We Offer Competitive salary aligned with industry benchmarks in Arlington Heights, IL. Health insurance including medical, dental, and vision coverage. Paid time off to support work-life balance and personal wellness. Retirement plan with company matching to help secure your financial future. Career development programs and training opportunities within a global healthcare leader. Supportive, safety-focused laboratory environment fostering innovation and quality excellence. Frequently Asked Questions What are the typical work hours for this position? This is a full-time, on-site role with standard laboratory hours, typically Monday through Friday. Is prior experience with Empower software mandatory? Yes, proficiency with Empower software for chromatographic data processing is essential for this role. Does this position offer opportunities for career advancemen