Senior Validator (f/m/x)
Sii Sp. z o.o.
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B2B
Hybrid
Senior
Toruń
Kraków
Lublin
Warszawa
+10
Expires Nov 22, 2026
1 day ago
In short
Senior Validator role focusing on IAM platform validation for GxP processes. Responsibilities include strategy definition, documentation, risk assessment, change control, and audit representation. Requires 5+ years in GxP validation, GAMP 5, EU GMP Annex 11, and FDA 21 CFR Part 11 knowledge. Offers stability, profit sharing, and benefits.
AI-written summary based on the listing content.
Technologies we use
About the project
Your responsibilities
- Defining and maintaining the validation strategy, intended use, scope, system boundaries, and lifecycle controls for the IAM platform supporting GxP processes
- Planning, preparing, reviewing, and approving complete and traceable validation documentation, ensuring adequate evidence is available before release and during operation
- Defining a testing approach based on risk and reviewing evidence for key IAM processes such as identity and account management, roles and access rights, and security controls
- Assessing changes, software releases, and configuration changes for GxP impact, and defining the required validation and regression testing
- Managing validation-related deviations and CAPAs in accordance with applicable procedures, including investigation support and verification of evidence before closure
- Keeping the platform in a validated state through effective change management, periodic reviews, and supplier oversight
- Clarifying responsibilities and data ownership across IAM and connected applications
- Working with Quality, System, and Process Owners, and service providers to resolve risks and deliver compliant solutions
- Representing IAM validation in audits and inspections, clearly explaining the validation scope, controls, risks, and evidence
- Identifying compliance gaps and leading improvements to simplify or automate assurance activities
Our requirements
- Minimum 5 years of experience in validation within regulated environments, specifically GxP processes
- Deep expertise in GxP, GAMP 5, and EU GMP Annex 11 regulations
- Strong understanding of FDA 21 CFR Part 11 and its implications for system validation
- Practical experience in creating and maintaining validation documentation, including requirements, risk assessments, and validation reports
- Proven ability to collaborate effectively with cross-functional teams, including Quality, IT, and Security
- Advanced level of English
Optional
- Experience with cloud-based IAM solutions
- Familiarity with automated validation tools
- Intermediate level of Spanish
What we offer
- Great Place to Work since 2015 - it’s thanks to feedback from our workers that we get this special title and constantly implement new ideas
- Employment stability - revenue of PLN 2.1BN, no debts, since 2006 on the market
- We share the profit with Workers - over PLN 76M has already been allocated for this aim since 2022
- Attractive benefits package - private healthcare, benefits cafeteria platform, car discounts and more
- Comfortable workplace – class A offices or remote work
- Dozens of fascinating projects for prestigious brands from all over the world – you can change them thanks to Job Changer application
- PLN 1 000 000 per year for your ideas - with this amount, we support the passions and voluntary actions of our workers
- Investment in your growth – meetups, webinars, training platform and technology blog – you choose
- Fantastic atmosphere created by all Sii Power People
| Published | 2026-10-23 |
| Source |
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29 days left
11/22/2026
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