Greetings !! Currently we are looking for *Senior Business Analyst *for one of our client, kindly advise me on your availability, I can be reached at *408-709-1760 ext 9662.* *Title: Senior Business Analyst * *Location: Waco, Texas * *Duration: 6+ Months* *Job Decription:* *Must have 6+ yrs in Pharma* - Project management experience, including strong organizational and time management skills. - Demonstrated and workable knowledge of cleanroom monitoring including but not limited to viable air sampling, total particulate sampling, viable surface sampling, pressure differential monitoring, and temperature & humidity monitoring. - Demonstrated knowledge of aseptic cleanroom environments. - Facility monitoring system design preferred. - Experience of Risk Assessments, Functional Specifications and System Validation procedures. - Current Good Manufacturing Practices (cGMP), Food and Drug Administration (FDA), and other regulatory requirements. Experience in a pharmaceutical manufacturing environment preferred, including GMP, Facilities and Manufacturing equipment Support Allergan Waco’s Facility Monitoring System upgrade project by providing Environmental Monitoring expertise in regards to cleanroom and pharmaceutical manufacturing environments. Additionally, Business Analyst will participate in the design, implementation, maintenance and support of the new facility monitoring system. This position will be responsible for: - Being a contributing member of the Facility Monitoring System upgrade team. - Gathering both technical and non-technical requirements, developing business process analysis, user/systems requirement analysis and specifications. - Participate in internal and external meetings relating to projects; provides summaries of meeting to appropriate person(s) and makes recommendations as appropriate. - Support processes to meet 21CFR Part 11 and Annex 11 standards to effectively manage information flow, data collection, and review activities. - Create, modify, and manage Standard Operating Procedures (SOPs), Work Instructions, and Risk Assessments, related to GMP systems. - Lead validation effort to perform validation/qualification activities to ensure data integrity and GMP system compliance. Incumbent has full authority to make decisions and/or take action that is required to carry out job duties. Thanks & Regards, Kumar Babul | Sr. Recruiter *ba...@tresourceinc.com* <ba...@tresourceinc.com> Technology Resource Group Inc. 1700 Park St, Unit 212, Naperville IL, 60563 Office : 408-709-1760 Ext: 9662 Fax: 408-213-8316 Gtalk :- babul...@gmail.com Yahoo :- babullad...@yahoo.com *www.tresourceinc.com* <http://www.tresourceinc.com/> -- -- To unsubscribe from this group, send email to cbe-software-engineer-unsubscr...@googlegroups.com For more options, visit this group at http://groups.google.com/group/CBE-Software-Engineer?hl=en --- You received this message because you are subscribed to the Google Groups "CBE Software Engineer" group. To unsubscribe from this group and stop receiving emails from it, send an email to cbe-software-engineer+unsubscr...@googlegroups.com. For more options, visit https://groups.google.com/d/optout.