IT Quality CSV Expert

Boost your career with us

Polpharma Biologics is a state-of-the-art biological R&D and manufacturing facility, one of the most modern in Europe. We have a fantastic, international team of experienced experts and dynamic young scientists with common goals and values. Biotechnology is our passion.

Together we develop medicines, offering a new hope to patients suffering from serious diseases. We create a passionate and friendly workplace environment. Join us!

Your responsibilities

  • Shape IT QMS processes in Polpharma Biologics Gdansk and cooperate within global organization for processes harmonization
  • Prepare, review and consult IT systems Validation Documentation through entire systems lifecycle in Polpharma Biologics
  • Drive initial Validation approach and key activities for projects in Digitalization program
  • Support GxP IT systems’ design and modifications within investment projects; plan & execute appropriate actions to keep GxP compliance in control
  • Authoring, reviewing and approving validation and qualification documentation and providing guidance to site staff on cGxP requirements for CSV
  • Initiating and performing the GxP risk and impact assessments
  • Taking part in IT related Deviation, CAPA and change control management
  • Conducting activities in accordance with the applicable cGMP, FDA CFR 21 Part 11, Annex 11 and internal procedures
  • Collaborating with QA, Engineering, other business units, contractors and vendor resources to ensure successful planning, execution and delivery of validation projects and documentation deliverables

If you have

  • Experience in designing and managing computerized systems in regulated environment
  • Experience in automation and IT projects management)
  • Higher directional education (Computer Science, Engineering or technical related fields)
  • Possess working knowledge of global GxP regulations (21 CFR Part 11, Data Integrity, Annex 11 & GAMP5)
  • Knowledge and understanding of latest industry data integrity trends, lifecycle management of computerized systems (e.g.incident- and error management , periodic reviews)
  • Minimum 2+ years of experience in computerized system validation within a regulated environment including performing a risk based end to end systems validation
  • Ability to recognize and solve problems independently, good organization and presentation skills, ability to work efficiently under time pressure
  • Strong change control, gap, root cause analysis experience
  • Experience in creation/maintenance & implementation of SOPs
  • Must be well-organized and a team player
  • Fluent English
  • Flexibility, communication skills, teamwork spirit

We offer

  • Private healthcare;
  • Life insurance;
  • Pension plan above national standards;
  • Relocation package;
  • Additional free day;
  • and more…
Join our Team!

Why you should work with us

Contact us
[email protected]