Project Manager

Should know GxP, Validation and possibly MES

GxP Documentation is must

Seeking a Project Manager with experience in Pharma/ Biotech/ Life Sciences/ Medical Device/ Healthcare or Manufacturing a must (Okay with either industry)

Responsibility:

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• 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.
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• Leads the effort to manage, and/or maintains validation of SAP S/4 HANA system.
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• Perform GxP and 21 CFR part 11 assessments and develop validation plan.
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• Develop functional risk strategy and perform functional risk assessment.
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• Review user business process documents and user requirements specification.
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• Review functional, technical and configuration design documents.
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• Prepare and/or review Configuration Qualification (CQ), Data Qualification (DQ), Installation Qualification (IQ), Operational Qualification (OQ) and performance Qualification (PQ) protocols.
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• Review the test scripts for the requirements and test scenario coverage.
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• Lead overall protocol executions, log and track defects.
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• Review the executed test reports for the proper documentation of test results and evidence.
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• Review the defects for proper documentation per the checklist.
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• Prepare and maintain the traceability matrix to ensure all the requirements are covered in design documents and tested.
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• Prepare and approve qualification summary report.
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• Participates in Corrective and Preventive Action (CAPA), Maintains quality metrics.
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• Maintain overall project and issue tracker and report routinely.
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• Support release management activities by reviewing and ensuring the pre-requisites are completed prior to the release.
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• Review Quality System support documentation including Standard Operating Procedures (SOP), Work Instructions (WI) and training materials.
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• Maintain day to day activities status tracker and report routinely.
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• Lead the team of validation engineers located in different time zones.
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Skills:

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• Excellent communication (oral and written) and attention to detail.
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• 8+ years in Computer System Validation in Life Science domain with minimum 3+ years of experience in managing large global SAP validation projects.
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• Ability to work independently and as part of a team, self-motivation, adaptability, and a positive attitude.
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• Excellent knowledge of GxP regulations, FDA and EMEA (European Medicines Evaluation Agency ) guidelines including 21 CFR Part 11.
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• Excellent knowledge of computer system validation and GAMP -5 standards.
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