Analytical Compliance Specialist II

Now Hiring: Analytical Compliance Specialist Lake County, IL - Hybrid We are seeking an experienced Analytical Compliance Specialist to support laboratory operations, analytical coordination, and quality system activities within a pharmaceutical environment. This is an excellent opportunity for a detail-oriented scientific professional with experience in analytical chemistry and GMP compliance to join a collaborative and fast-paced team. Location: Lake County, IL (1401 Sheridan Road) Contract Duration: 1 Year

JP34079

Position Overview The Analytical Compliance Specialist will support a variety of laboratory and quality-related activities to help ensure efficient operations, compliance with GMP requirements, and effective coordination of analytical workflows across internal teams and external partners. The ideal candidate will bring strong organizational skills, attention to detail, and the ability to manage multiple priorities in a regulated pharmaceutical environment. Key Responsibilities Support quality control coordination activities for drug substance and drug product stability programs, including study management within LIMS Coordinate shipment logistics for laboratory samples and materials as needed Support laboratory instrument documentation activities including calibration, qualification, maintenance, and repair records Assist with outsourced analytical testing coordination and vendor communication Partner with subject matter experts to coordinate routine and non-routine analytical activities Support troubleshooting, issue tracking, and follow-up related to laboratory and quality operations Ensure compliance with GMP standards and applicable quality system requirements Maintain accurate documentation, reports, and laboratory records in accordance with compliance expectations Required Qualifications Bachelor’s or Master’s degree in Chemistry, Biochemistry, Pharmaceutical Sciences, or related scientific discipline Experience working within pharmaceutical quality systems and GMP-regulated environments Experience supporting analytical development or pharmaceutical laboratory operations preferred Strong organizational, communication, and coordination skills Ability to manage multiple priorities and collaborate cross-functionally High attention to detail with strong commitment to data integrity and compliance Why Join This Opportunity? Work within a highly collaborative pharmaceutical laboratory environment Gain exposure to analytical operations, quality systems, and compliance activities Opportunity to support impactful drug substance and drug product programs Hybrid work schedule offering flexibility and team collaboration #J-18808-Ljbffr K3-Innovations, Inc.