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Sii Sp. z o.o.

Senior Validator (f/m/x)

Sii Sp. z o.o. Show all offers
B2B
Hybrid
Senior
Bydgoszcz
Warszawa
Rzeszów
Lublin
+10
Expires Nov 22, 2026
1 day ago

In short

Senior Validator needed for IAM platform in regulated (GxP) environments. Responsibilities include validation strategy, documentation, risk assessment, change control, and audits. Requires 5+ years of GxP experience, knowledge of GAMP 5, EU GMP Annex 11, FDA 21 CFR Part 11, and advanced English. Optional Spanish, cloud IAM, or automation tools experience.

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
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