cgmp jobs in Chicago

Katalyst CRO in Illinois is seeking a Change Control Specialist to support change management and documentation within a cGMP-regulated analytical environment. The role centers on coordinating, managing, and tracking change control workflows across analytical methods, validation, and instrumentation.The ideal candidate has strong experience in change...

Univar Solutions in the United States is seeking a Senior Regional Quality Manager to guide quality systems, regulatory compliance, and business quality plans across districts. You will support operations leadership for audits, drive improvements, and coordinate initiatives at a national level with emphasis on cGMP, FDA, ISO and other standards. The role...

Univar Solutions in the United States is seeking a Senior Regional Quality Manager to guide quality systems, regulatory compliance, and business quality plans across districts. You will support operations leadership for audits, drive improvements, and coordinate initiatives at a national level with emphasis on cGMP, FDA, ISO and other standards. The role...

Jubilant Radiopharmacies is seeking a Site Quality Lead to ensure radiopharmaceutical manufacturing meets FDA, cGMP, and internal quality standards. You will oversee quality systems, support sterile operations, and partner with operations, QC, and corporate quality teams to drive patient safety.The role emphasizes meticulous process improvement,...

Univar Solutions in the United States is seeking a Senior Regional Quality Manager to guide quality systems, regulatory compliance, and business quality plans across districts. You will support operations leadership for audits, drive improvements, and coordinate initiatives at a national level with emphasis on cGMP, FDA, ISO and other standards. The role...

cGMP Consulting Inc. is seeking a motivated technical writer to lead documentation activities for quality system records in a GMP environment. You will author deviations, change controls, and CAPAs, while coordinating with Manufacturing, Quality, and Engineering teams to ensure compliance and accuracy. The ideal candidate has strong writing skills, attention...

VantageSpecialtyChemicals in Chicago, IL is seeking a Production Technician/ Warehouse Operator for the Chicago Oleo Plant. You will perform material movements, load/unload, and operate pumps while adhering to cGMP and ISO procedures to ensure quality and safety throughout production. The role requires a High School Diploma or GED and at least six months in...

Vantage Oleochemicals, Inc in Chicago, IL seeks a Production Technician to move materials, operate pumps and valves, and ensure safe, compliant plant operation. You will document activities, maintain inventory, and support maintenance preparation while adhering to cGMP and safety rules. The role requires a High School Diploma or GED and forklift experience;...

The Validation Specialist II is responsible for developing, implementing, and maintaining validation programs that ensure manufacturing processes, equipment, software systems, controlled environments, and cleaning processes remain compliant with regulatory requirements and company standards. This role independently plans and executes validation activities,...

GForce Life Sciences is seeking a hands-on Laboratory Manager to oversee operations, staff, and equipment for drug-device combination-product testing. You will partner with Engineering, Quality and Operations to improve capacity, throughput, and client commitments.You will manage daily priorities, lead method development and testing for autoinjectors and...

Senior Environmental Health & Safety ManagerThe Senior Environmental Health & Safety (EHS) Manager is responsible for leading and overseeing comprehensive EHS programs across two sites in New Jersey and Chicago. This role drives the development, implementation, and continuous improvement of initiatives that promote a safe and compliant work environment...

At Jubilant Radiopharmacies, we support patient care by producing and delivering high-quality radiopharmaceutical products that help clinicians diagnose and treat disease. Our teams work with purpose, collaboration, and a strong commitment to safety and compliance. We value people, empower growth, and encourage a culture where individuals can do their best...

RoleSenior executive responsible for overseeing Xeris’s outsourced manufacturing, supply chain, and device engineering functions across a diverse portfolio including small molecules, peptides, and biologics.Objectivesensure seamless product lifecycle management from clinical development to commercialization and post-approval, maintaining high quality and...

Manufacturing Associate III (DP)The Manufacturing Associate III (DP) is a regular full-time non-exempt position at Kashiv BioSciences, LLC, in Chicago, IL. This employee will be responsible for the formulation, filtration, and aseptic filling of drug products for clinical and commercial human use. Employees employ aseptic techniques while working in...

At Ecolab, making the world a cleaner, safer place is our business. In the Life Sciences division, we are committed to providing complete solutions for the Personal Care industry. We achieve this by providing comprehensive solutions and technical know-how focused on ensuring product quality and safety in cleaning, sanitation and contamination control while...

Site Quality Lead Location: Chicago (Northbrook). IL About Jubilant Radiopharmacies At Jubilant Radiopharmacies, we support patient care by producing and delivering high‑quality radiopharmaceutical products that help clinicians diagnose and treat disease. Our teams work with purpose, collaboration, and a strong commitment to safety and compliance. We...

QMS Specialist - Biologics Manufacturing 📍 Chicago, IL 🏢 On-site | Full-time, Permanent Global Life Science Hub is supporting a growing commercial-stage biologics manufacturer looking to expand its Quality Systems team in Chicago. We are looking for a QMS Specialist with experience directly supporting GMP biologics manufacturing , ideally across...

About Us At cGMP Consulting, we specialize in providing expert validation, qualification, and compliance services to the life sciences industry. Our team works with clients to ensure their facilities, equipment, and processes meet regulatory standards, enabling the safe and efficient production of pharmaceuticals.cGMP Consulting is based in Lake Forest, IL....

Permanent, Technical Project Manager II, Combination ProductsDo not pass up this chance, apply quickly if your experience and skills match what is in the following description.SummaryOur client, a small medical device development company, has engaged GForce Life Sciences to provide a Project Manager II. This position will report to aDirector of Engineering....

cGMP Consulting is seeking a detail-oriented professional to lead technical evaluations and qualification of raw materials for medical devices. You will review testing specifications, assess supplier documentation, and establish acceptance criteria to ensure materials meet product and regulatory requirements.You will collaborate with R&D, analytical...