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You will be updated with latest job alerts via emailYour Key Responsibilities
Lead the Development and Implementation: Spearhead the creation and execution of a comprehensive computer system validation policy ensuring alignment with current regulatory standards (e.g. 21 CFR Part 11 OECD 17 OECD 17 supplement 1 EU-GMP Annex 11 GAMP 5) for Confidence Validation Services.
Drive Global Electronic Systems Initiatives: Lead the implementation of new global electronic systems such as an eQMS ensuring seamless integration and compliance.
Post-Implementation: Manage the ongoing maintenance and updates of electronic systems ensuring optimal performance and compliance.
Risk Assessment and Compliance: Conduct risk assessments compile compliance reports manage deviations and ensure all documentation meets quality and regulatory standards.
Create and oversee CSV protocols including IQ OQ and PQ ensuring thorough validation of electronic systems.
Oversee the document lifecycle from creation and revision to storage
Support administration of electronic systems ensuring efficient operation
Offer basic CSV training to enhance team capabilities and ensure compliance
Collaborate intimately with all stakeholders to guarantee systems comply with project and regulatory standards
Participate in regular project meetings to align with system owners and management ensuring project requirements are met and issues are resolved.
Supervise vendor interactions including reviewing and tracking vendor deliverables and system qualifications
Collaborate with global/regional site quality units and functions to ensure harmonized practices
Any ad hoc duties to collaborate and contribute to other activities as identified Confidence management
What will convince us
Advanced Educational Background: Masters degree or higher in a relevant field (e.g. Engineering Computer Science Life Sciences)
Industry Experience: Minimum of 5 years in a GMP and/or GLP-regulated environment with a proven track record in validating cloud solutions such as eQMS LIMS/ELN and stand-alone computer systems.
Regulatory Expertise: Extensive knowledge of CSV regulatory requirements (e.g. 21 CFR Part 11 OECD 17 OECD 17 supplement 1 EU-GMP Annex 11 GAMP 5).
Independent Deliverable Generation: Ability to independently generate CSV deliverables ensuring high-quality outputs.
Experience in working in a cross-cultural set up
Ability to develop realistic work plans set personal goals that align with company goals
Superior organizational communication and documentation skills
Self-driven and methodical way of working ensuring thoroughness and accuracy
Fluent in English with excellent communication skills
About Sartorius
Sartorius is part of the solution in the fight against cancer dementia and many other diseases. Our technologies help translate scientific discoveries into real-world medicine faster so that new therapeutics can reach patients worldwide.
We look for ambitious team players and creative minds who want to contribute to this goal and advance their careers in a dynamic global environment.
Join our global team and become part of the solution. We are looking forward to receiving your application.
Experience:
Unclear Seniority
Full-Time