What are the responsibilities and job description for the Validation Engineer II - CSV and Compliance Support position at Planet Pharma?
Responsibilities
- Work to support the ITOT System owners in tasks associated with the lifecycle of computer system, ie. maintenance, validation, documentation, testing.
- Create/update Computer System validation and lifecycle support documentation, as the need arises, for ITOT computer systems (DeltaV, PI, MES, SCADA, LyoPLus, FIT, BAS, WAGIT). Systems will fall between Level 2 and 3 of the ISA-95 model.
- Help perform MILE (annual system maintenance) activities for ITOT Systems. For example, create, update, execute, or review installation protocols, test protocols, etc.
- Own Quality Management System records (CAPA, Planned Events, Deviations) and orchestrate completion of activities needed.
- Perform system periodic reviews- This entails performing data collection from the deviations database on the past 3 years worth of planned and unplanned events, review impact on systems validated state and draft reports.
- Support System Owner squad in the overall procurement, development, integration, modification, operation, maintenance, and retirement of ITOT systems.
- Support validation activities, generation, approval and execution of validation protocols
- Assist System Owners in system maintenance activities such as Periodic System Audit Trail Review, account audits, etc.
- Creating reports for various systems on demand
- Work with the System Owners and Business Process Owners for the upgrade/patching and changes to the system to ensure GMP compliance.
- Support on documents management systems (Veeva, Condor, eVal)
- Support the team with administrative tasks, such as document formatting, document routing.
- Collaborate with local and global stakeholders in defining and completing validation and compliance activities.
- Attend Quality Huddle Meetings
- Provide Quality Metrics
- Align with global Validation protocols and policies
- Bachelor of Science or equivalent in computer science, engineering, life sciences, or related field.
- Minimum 5 years experience in Computer systems Validation frameworks (CSV/CSA, GAMP), preferably in the Pharma industry.
- Knowledge of or experience with the following technical areas is preferred: SCADA, OSI-PI, Siemens Desigo, Rockwell Factory Talk Pharmasuite, DeltaV, Manufacturing Execution Systems (MES) Systems administration and EBR recipe authoring, software development,
- Good understanding of the ISA-95 model. Experience working with Level 2 and Level 3 systems is required. Experience working with Level 1 systems is a plus.
- Knowledge of Food and Drug Administration regulations/guidance (i.e. CFR 21 FDA Part 11, Annex 11, EU GMP Annex 1, GxP practices) and Data Integrity principles.
- Good understanding of system and data integrity risk assessment concepts.
Salary : $60 - $75