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Computer System Validation Professional

Computer System Validation Professional

Sartorius

5 - 10 years

7 - 12 Lacs

bengaluru

Posted:2 hours ago| Platform:

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Skills Required

computer science computer system validation manager quality assurance compliance risk assessment cloud glp life sciences gmp management

Work Mode

Work from Office

Job Type

Full Time

Job Description

Computer System Validation (CSV) Professional
Join Sartorius as a Senior Computer System Validation (CSV) Professional and become a key player in driving harmonization, compliance, and quality assurance within our Confidence Validation Services Quality team. In this impactful role, you will lead the establishment of a harmonized validation policy, ensuring our computer systems are compliant with the latest regulatory standards (e.g., 21 CFR Part 11, OECD 17, OECD 17 supplement 1, EU-GMP Annex 11). Your expertise will be instrumental in implementing state-of-the-art tools such as an eQMS and ELN/LIMS, enhancing our service departments efficiency and quality. Additionally, you will have a chance to elevate our quality assurance processes by driving the implementation of an eQMS as well as to contribute to the global harmonization across all Confidence Validation Services sites. This full-time hybrid position offers the flexibility of remote work while requiring some on-site presence to foster collaboration and innovation.

Your 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

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Biotechnology, Laboratory Equipment

Göttingen

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Computer System Validation Professional