Possible locations
  • Warsaw
  • Bialystok
  • Bydgoszcz
  • Czestochowa
  • Gliwice
  • Gdansk
  • Katowice
  • Cracow
  • Lublin
  • Lodz
  • Pila
  • Poznan
  • Rzeszow
  • Wroclaw
  • Remote work
Technologies & tools
  • CSV
  • GAMP

Referring to the recommendations related to coronavirus on limiting meetings, we are open to conducting online recruitment interviews through video conferences.

Join our team working on projects of one of the largest pharmaceutical companies in the world and have a real impact on the lives and health of more than 15 million patients! By implementing the projects of Sii's key, long-standing client, you will get the chance to develop in the field of R&D, clinical trials and global services. You will work based on Agile methodologies, using modern tools and technologies.

We will ensure the continuity of your employment, at the same time giving you the opportunity to change your project or project team at any time. You will be also offered regular in-house training and specialist workshops. Remote work, work at the office or flexible working hours – the choice is 100% yours.

Your role

  • Determine validation approach, identify deliverables needed or impacted by a project / enhancement / or change for GXP computerised systems
  • Responsible for the review of software documentation according to CSV corporate SOP's, and regulatory guidance
  • Provide estimates and forecast validation activities for a project
  • Author validation plans/reports, reviews test plans/reports (and other deliverables) to asses and notify that system is ready to go life
  • Verification of testing plans, activities, deliverables and records, provide consultancy on test related deviations and corrective actions

Your skills
  • 3+ years experience in IT & Software Validation (CSV, GAMP), preferably in pharma environment
  • Experience in leading validation for projects and systems maintenance, as well as in authoring validation plans, reports and deliverable registries
  • Experience in software development lifecycle processes (SDLC), models, standards in pharmaceutical industry (or other regulated)
  • Experience in maintenance and support of applications under global inspection agencies, CFR 21 FDA Part 11, Annex 11
  • Fluent (written and spoken) English – we work in international teams and set ups

Why Sii

Great Place to Work since 2015

it’s thanks to our workers’ opinions that we get the title and implement new ideas

Dozens of fascinating projects

for prestigious brands from all over the world, based on a variety of technologies

Employment stability

Is your project coming to an end? Do you want to change it? We’ll find you a new one! We have an app for this – Job Changer

Financial stability

revenue of 225 EUR M, no debts, preferred supplier status for many clients

PLN 500 000 per year for your ideas

with this amount, we support the passions and voluntary actions of our workers

5 000+ experts

to learn from and share your experience with

Investment in your growth

meetups, webinars, training platform and technology blog – you choose

Comfortable workplace

class A offices or remote work

Friendly management

quick decision-making, we’re all on a first-name basis

True values

these are not empty words – we’re guided by them every day

Fantastic atmosphere

created by all Sii Power People

Attractive benefits package

private healthcare, MyBenefit platform, car discounts and more

Join us

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