CSV Specialist
Duchnice
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:
  • 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 CSV related Deviation, CAPA and change control management;
  • Managing CSV status of technical systems, equipment and production installations;
  • Conducting activities in accordance with the applicable cGMP, FDA CFR 21 Part 11, Annex 11 and internal procedures;
  • Collaborating with QA, IT, Engineering, other business units, contractors and vendor resources to ensure successful planning, execution and delivery of validation projects and documentation deliverables.
If you have:
  • 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. alarm management, incident- and error management , periodic reviews);
  • Minimum 3+ 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;
  • Must be detail oriented, with strong analytical and problem solving skills, and to effectively research, troubleshoot, and solve challenging problems involving integrated systems;
  • Fluent English;
  • Flexibility, communication skills, teamwork spirit.
Join our Team!
Why you should work with us
Contact us
career@polpharmabiologics.com

Podobne oferty

inzynier-jakosci oferta pracy

LOT Aircraft Maintenance Services Sp. z o.o.

mazowieckie / Warszawa

wczoraj

Inspektor Techniczny w Obszarze Badań Nieniszczących

Wymagania: Wykształcenie średnie techniczne lub wyższe (preferowane kierunki: Lotnictwo, Mechanika i Budowa Maszyn, Mechatronika) Uprawnienia NDT w metodzie...

Szczegóły
inzynier-jakosci oferta pracy

TPV Displays Polska Sp. z o.o.

lubuskie / Gorzów Wielkopolski

2022-01-14

Inżynier ds. zapewnienia jakości dostawców

Do zadań na tym stanowisku należy: Codzienna współpraca z dostawcami, w celu zapewnienia jakości dostarczanych materiałów, Rozwiązywanie bieżących...

Szczegóły