Document Control Specialist I

Job Title: Document Control Specialist I Job Location: Round Lake, IL, 60073 Job Duration: 09 Months+ (Possible Extension) Pay Range: $21.00 to $22.00/hr on W2 Note: The candidate must not be allergic to penicillin or cephalosporin drugs. Job Summary: The Quality Document Technician plays a crucial role in supporting quality systems by ensuring that essential documents are created, organized, and available for use in manufacturing and product release. Responsibilities: Makes detailed observations, analyzes data, and interprets results. Create, verify, and distribute quality documentation required for manufacturing. Support Document Center Technicians with standard office work and for batch release. Maintains department equipment and inventory levels for controlled materials. Identifies process improvements and escalates to Quality Supervision and/or Management. Ability to work independently and as part of a team in a fast-paced environment. Requirements: Basic science, math, and computer skills (including Microsoft Word and Excel) are required. Good writing, verbal communication, and problem-solving skills are required. Ability to work in a team environment and make independent decisions based on procedural and regulatory requirements. It is desirable for the candidate to have experience with the requirements of current Good Manufacturing & Documentation Practices in pharma manufacturing facilities. The candidate must be able to work flexible hours in a dynamic environment with minimal direct supervision. Will work in both Drug Delivery and Penicillin facilities as needed. Overtime may be required to meet the production schedule. 6 months of experience in manufacturing/quality preferred HS Diploma or equivalent is required Basic science, math, and digital literacy (including Microsoft Word and Excel) are required. Strong writing and verbal communication abilities, as well as problem solving capabilities are needed. Attention to detail and organization are highly desired It is desirable for the candidate to have experience with the requirements of current Good Manufacturing & Documentation Practices in medical devices/pharma manufacturing facilities. Be able to work flexible hours in a dynamic environment with minimal direct supervision. Ability to work some Saturdays is required. The ability to work on some weekends is required. Desirable Skills & Experience: Strong attention to detail and organizational skills. Experience in GMP and Documentation Practices in medical devices or pharma manufacturing.