* This position is responsible for leading and performing activities in support of creating and maintaining GxP (GMP, GCP, and GLP) quality and compliance environment for SAP S/4 HANA.
This position is also responsible for monitoring Computer System validation (CSV) as well as compliance with GxP regulations and 21 CFR Part 11.
* Leads the effort to manage, and/or maintains validation of SAP S/4 HANA system.
* Perform GxP and 21 CFR part 11 assessments and develop validation plan.
* Develop functional risk strategy and perform functional risk assessment.
* Review user business process documents and user requirements specification.
* Review functional, technical and configuration design documents.
* Prepare and/or review Configuration Qualification (CQ), Data Qualification (DQ), Installation Qualification (IQ), Operational Qualification (OQ) and performance Qualification (PQ) protocols.
* Review the test scripts for the requirements and test scenario coverage.
* Lead overall protocol executions, log and track defects.
* Review the executed test reports for the proper documentation of test results and evidence.
* Review the defects for proper documentation per the checklist.
* Prepare and maintain the traceability matrix to ensure all the requirements are covered in design documents and tested.
* Prepare and approve qualification summary report.
* Participates in Corrective and Preventive Action (CAPA), Maintains quality metrics.
* Maintain overall project and issue tracker and report routinely.
* Support release management activities by reviewing and ensuring the pre-requisites are completed prior to the release.
* Review Quality System support documentation including Standard Operating Procedures (SOP), Work Instructions (WI) and training materials.
* Maintain day to day activities status tracker and report routinely.
* Lead the team of validation engineers located in different time zones.
Skills:
* Excellent communication (oral and written) and attention to detail.
* 8+ years in Computer System Validation in Life Science domain with minimum 3+ years of experience in managing large global SAP validation projects.
* Ability to work independently and as part of a team, self-motivation, adaptability, and a positive attitude.
* Excellent knowledge of GxP regulations, FDA and EMEA (European Medicines Evaluation Agency ) guidelines including 21 CFR Part 11.
* Excellent knowledge of computer system validation and GAMP -5 standards.
Job Type: Contract
Pay: $40.
00 - $55.
00 per hour
Expected hours: 40 per week
Experience level:
* 10 years
Schedule:
* 8 hour shift
License/Certification:
* PMP (Preferred)
Work Location: On the road
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