Process Validation Coordinator

Job description

The primary focus of this position is to provide sample management and associated logistical support during a drug substance process validation campaign. Key responsibilities include the following. 1. Create and maintain master sample plan by assembling sampling requirements from all applicable activities, laboratories, and stakeholders associated with the process validation campaign 2. Maintain and enforce sample management workflow and processes 3. Provide data verification and documentation support to ensure alignment of the master sample plan with GMP documentation such as protocols and batch records, and laboratory information system 4. Support ad-hoc, supplemental sample requests utilizing a paper-based or electronic sample request workflow; coordinate with sample requestor and manufacturing on ad-hoc/supplemental sample requests 5. Daily coordination with manufacturing to confirm that sampling plan and requirements are understood and followed 6. Daily check-in with laboratories and sample requestor on the receipt of samples 7. Escalation and coordinate resolution of sampling related issue including but not limited to missed sample, production plan changes, sample plan changes 8. Query and collate laboratory results from submitted samples; provide data verification and documentation support to summarize laboratory results in validation and technical reports. 9. Provide supplemental logistical, administrative, and documentation support for the preparation of, and the duration of the process validation campaign Required Skills: Proficiency in Microsoft Word and Excel; prior working experience with electronic laboratory information management system (LIMS) • A B.S or M.S degree in any science related discipline is preferred • Should possess 4-7 years of experience in Biopharmaceutical manufacturing experience. • Should possess 4-7 years of experience in Documentum • Experience in sample management and electronic laboratory information management system is a plus • Working experience with documentum system • Prior experience with biologics drug substance manufacturing, quality control, and/or validation A Few Words About Us Integrated Resources, Inc is a premier staffing firm recognized as one of the tri-states most well-respected professional specialty firms. IRI has built its reputation on excellent service and integrity since its inception in 1996. Our mission centers on delivering only the best quality talent, the first time and every time. We provide quality resources in four specialty areas: Information Technology (IT), Clinical Research, Rehabilitation Therapy and Nursing. This is Contract position with my direct client