job summary: As the largest staffing and recruitment agency in the world, we can commit to finding you the perfect role that gives you the opportunity to learn and grow in the life sciences arena. Utilizing a recruiter for your job search gives you access to a large network of top employers as well as detailed information about hundreds of positions. We supply prestigious life sciences and biopharma companies with job seekers like you to achieve their business goals. If you're looking for a position where you can serve as an asset to your company while making a difference in others' lives, we have the ideal position for you! location: Melrose Park, Illinois job type: Contract salary: $24 - 25 per hour work hours: 8 to 4 education: High School responsibilities: Classifies a wide range of technical documents received by Central File including Production Batch Records, Validation/Qualification protocols, CWOs (Critical Work Orders), testing and release records for incoming chemical raw materials, Stability test records, Laboratory Notebooks and reports for numerous facility systems, equipment and instruments, facility log books documenting manufacturing process, operation and maintenance of equipment, etc. Other documents include FDA historical records of contracts, inspections, responses to observations, all of which are critical to substantiate and demonstrate positive compliance status of the manufacturing facility.Performs subject technical indexing function by assigning appropriate document identification using database for storage and retrieval.Indexes and archives documents received at the Central File for secure storage.Provides input on preparation and writing of SOPs for the Central File and assists in ongoing revision/update of such procedures.Assigns priorities for and provides timely retrieval of records requested.Establishes and manages the retention schedule for older, inactive files, determines when documents are transferred for off-site archival storage.Accurately maintains Central File Database Index of validations and STAD reports.Assures proper organization and housekeeping of Central File areas at all times.Ensures the integrity and security of all Central File documents and filing areas.Coordinates the receipt of all manufacturing documents and product testing reports. qualifications: High school graduate with some college preferred.3-5 years' experience in the pharmaceutical industry.Knowledge of computerized record tracking systems.Good knowledge of validation and manufacturing processes with experience in handling associated controlled documents.Excellent organizational skills required. skills: SOP, FDA, Quality Assurance 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 HRsupport@randstadusa.com. 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 health, an incentive and recognition program, and 401K contribution (all benefits are based on eligibility). Applications accepted on ongoing basis until filled.