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*Please Share Resumes at               dil...@tresourceinc.com
<dil...@tresourceinc.com>*

*Job Title: Business Analyst with Strong Pharma Experience*

*Duration: 6 + Months*

*Location: Waco, Texas *







*Position Details*

Job Title/Role

Senior Business Analyst

Mandatory Skills

10 Yrs of exp which includes 7-8 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.

Desired Skills

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.



Dileep Pali | Sr. Recruiter |

Technology Resource Group Inc.

1700 Park St, Unit 212, Naperville IL, 60563
Office: 408-709-1760 Ext : 9957

G talk: <http://www.tresourceinc.com/> palidileep |Yahoo id : palidileep

dil...@tresourceinc.com

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