Project Manager at The Remas Company, LLC in La Verne, California, United States

Job description

• 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)

Responsibilities

• 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.

Requirements

• 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.

Skills

Required

• GxP
• Validation
• MES (possibly)
• GxP Documentation
• Computer System Validation (CSV)
• GAMP-5 standards
• FDA and EMEA guidelines
• 21 CFR Part 11
• SAP S/4 HANA
• Attention to detail
• Self-motivation
• Adaptability