QA Document Specialist
$20 - $24.5 per hourRandstad USA
Advance your career with a top-tier global pharmaceutical leader in Melrose Park, IL! We are seeking a reliable, detail-oriented QA Documentation Specialist for an immediate, full-time on-site role (Monday-Friday, 8:00 AM-5:00 PM). This 3-month contract position offers strong potential for extension or conversion based on performance and ongoing business needs. location: Melrose Park, Illinois job type: Contract salary: $20.00 - 24.50 per hour work hours: 9 to 5 education: Bachelors Responsibilities Issue 8 to 12 batch production records weekly to active packaging and manufacturing lines. Coordinate and review weekly production schedules to identify and issue required product records. Navigate and maintain cloud-based Electronic Document Management Systems (EDMS). Perform document editing, updates, and formatting in Microsoft Word for batch record revisions. Self-manage daily and weekly workflows independently to support continuous production output. Qualifications Required Hands-on experience managing regulated documentation within GMP-compliant environments. High proficiency in Microsoft Word for document editing, formatting, and template updates. Preferred Prior pharmaceutical, biotech, or medical device industry background. Direct experience operating EDMS, Documentum, TrackWise, or similar cloud documentation tools. Bachelor's degree (Associate's degree or High School Diploma with relevant experience accepted). Solid computer systems software navigation skills. Proven reliability, accountability, and strong self-management skills. Skills Good Manufacturing Practices (GMP) Quality Assurance (QA) Batch Record Equal Opportunity Employer: Race, Color, Religion, Sex, Sexual Orientation, Gender Identity, National Origin, Age, Genetic Information, Disability, Protected Veteran Status, or any other legally protected group status. At Randstad, we welcome people of all abilities and want to ensure that our hiring and interview process meets the needs of all applicants. If you require a reasonable accommodation to make your application or interview experience a great one, please contact View email address on click.appcast.io. Pay offered to a successful candidate will be based on several factors including the candidate's education, work experience, work location, specific job duties, certifications, etc. In addition, Randstad offers a comprehensive benefits package, including: medical prescription dental vision AD&D life insurance offerings short-term disability 401K plan (all benefits are based on eligibility) This posting is open for thirty (30) days. Required Hands-on experience managing regulated documentation within GMP-compliant environments. High proficiency in Microsoft Word for document editing, formatting, and template updates. Preferred Prior pharmaceutical, biotech, or medical device industry background. Direct experience operating EDMS, Documentum, TrackWise, or similar cloud documentation tools. Bachelor’s degree (Associate's degree or High School Diploma with relevant experience accepted). Solid computer systems software navigation skills. Proven reliability, accountability, and strong self-management skills. #J-18808-Ljbffr Randstad USA
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