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*Position: Business Analyst*

*Location: Waco, TX*

*Duration: 6+ Months*



Job Details:

·         7 -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.



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 & Best Regards

SUPRIYA PATHAK

Resource Logistics Inc.

505 Thornall Street, Edison, NJ 08837

Phone: (732) 553-0566 Ext 41

 Email- [email protected]

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