Label Quality Associate
The Fountain Group · Lake County, IL · Yesterday
HybridOTHR$31–$34/hrContract
The Fountain Group is a national staffing firm and we are currently seeking a --------Label Quality Associate for a prominent client of ours. This position is in North Chicago, IL 60064 Details for the position are as follows: Clinical Label Quality Associate 📍 Location: Hybrid (Onsite Tuesday/Wednesday/Thursday after training) 💲 Pay: $31-34/hr Top Requirements Bachelor's degree preferred (Science, Engineering, English, Business or related preferred)Bachelor's + 1 year experience, Master's + internship, or High School + 4 years relevant experienceExceptional attention to detail and accuracyStrong computer skills with the ability to quickly learn new systemsData entry, document review, or quality review experienceExcellent organizational, communication, and time management skills Preferred Experience GMP or other regulated industry experience (pharma, biotech, medical device, food, etc.)Quality review/QA experienceExperience proofreading or reviewing controlled documentsLabel creation or labeling experience is a plus but not required Day-to-Day Responsibilities Transfer clinical labels into a new labeling systemCreate and edit clinical labels based on source documentationProofread labels for accuracy, consistency, and regulatory complianceCoordinate label approvals and documentationWork closely with label designers, project managers, and global stakeholdersEventually manage assigned studies and labels independently Ideal Backgrounds Quality Assurance AssociateDocumentation SpecialistGMP Documentation CoordinatorClinical Labeling AssociateRegulatory Documentation AssociateManufacturing QA SpecialistQuality Control Documentation SpecialistTechnical Writer (regulated industry)Packaging Documentation CoordinatorMedical Device or Pharmaceutical QA Associate Manager Insights This team supports clinical supply labeling for packaging operations. Labeling experience is not required—the manager is more interested in candidates with quality review experience, especially in a GMP or other regulated environment. Candidates must be highly detail-oriented, able to follow established processes, and comfortable handling documentation with a high degree of accuracy. Strong potential for growth into independently managing labeling projects and collaborating with global teams once trained. By applying for this job, you agree to receive calls, AI-generated calls, text messages, or emails from and its affiliates, and contracted partners. Frequency varies for text messages. Message and data rates may apply. Carriers are not liable for delayed or undelivered messages. You can reply STOP to cancel and HELP for help. You can access our privacy policy at Privacy Policy