#PolpharmaBiologics to jeden z najnowocześniejszych ośrodków badań i rozwoju oraz produkcji leków biologicznych w Europie. Jesteśmy międzynarodowym zespołem doświadczonych ekspertów oraz ambitnych młodych naukowców posiadających wspólne cele i wartości. Biotechnologia jest naszą pasją, dzięki której wspólnie opracowujemy leki będące nadzieją dla pacjentów cierpiących na ciężkie choroby. Razem tworzymy przyjazne miejsce pracy, w którym możemy się rozwijać oraz realizować swoje ambicje. Chcielibyśmy, abyś do nas dołączył.
specjalista (mid) / kierownik/koordynator kontrakt B2B pełny etat
557 dni
Key Responsibilities: Establishing and maintaining training curriculum for Polpharma Biologics employees of a group functions Development, TechOps, Quality, Enabling Functions, etc. Administrating and organizing training; Creating training plans according to the functions’ requirements /...
specjalista mid / senior / ekspert umowa o pracę pełny etat
557 dni
Acting as a Senior Stability Specialist in the Quality Control. Acting as a major contact point for topics related to stability study in a given project, from development to discontinuation of production. Coordinating analytical activities and compilation of quality documents on the stability of the...
Your Role Polpharma Biologics is already finalizing its new R&D and manufacturing facility in Duchnice, Poland. In this new state-of-the facility we are currently establishing Research & Development department, to develop, optimize and characterize protein production processes from the laboratory...
As a Project Manager PMO you are responsible for leading all the project related activities by acting as project/program manager, assuming the responsibility for over-seeing full project scope from initiation to closure, harmonizing the needs of all the departments involved (Engineering, Production,...
specjalista mid / senior / ekspert umowa o pracę pełny etat
561 dni
Jako Starszy Specjalista/Ekspert będziesz brał udział w procesie przygotowywania budżetów, planów i prognoz finansowych, kontrolowanie ich realizacji, sporządzanie raportów oraz analiz finansowych i ekonomicznych w zakresie projektów badawczo-rozwojowych. Poziom stanowiska dopasujemy do...
specjalista (mid) / kierownik/koordynator umowa o pracę pełny etat
561 dni
Key responsibilities for this role include: Knowledge and Lab experience in some or all the following is an advantage; Inhibition of Proliferation assay, Potency assays, Binding assay, Maintenance of cell lines for cell-based bioassay and ELISA; Protocol generation and review – method Transfer /...
Your responsibilities Plan, managed, support and implement the quality assurance of process, cleaning, transport and sanitization/sterilization validation program consisting of entire system lifecycle in order to ensure compliance with relevant regulatory requirements and industry...
The Senior Specialist, Quality Control operation Biologics and supports Commercial quality activities at the Company Gdańsk, Poland . The successful candidate will have accountability for Good Manufacturing Practice (GMP) compliance, ensuring QC release testing of drug substance and drug product....
Your responsibilities Plan, managed, support and implement the quality assurance of process, cleaning, transport and sanitization/sterilization validation program consisting of entire system lifecycle in order to ensure compliance with relevant regulatory requirements and industry...
Your responsibilities Drug Substance and Drug Product of biosimilars Review and maintain adherence to QC testing including validation, Specifications, and COA’s. Oversee any deviations or planned changes in QC and ensure authorization is in accordance with defined systems and relevant authorities....
kierownik/koordynator / menedżer umowa o pracę pełny etat
561 dni
Your role Coordinating work in the Microbiological Team in the scope of tasks related to the microbiological tests of final products, intermediate products and raw materials. Managing and organizing work related to microbiological monitoring of the production environment. Implementation of new...
Specjalista ds. Zgodności Jakości będzie odpowiedzialny za pomoc Kierownikowi ds. Kwalifikacji Dostawców w opracowaniu, wdrożeniu i nadzorowaniu funkcjonowania Systemu Zarządzania Jakością. Wsparcie w przygotowaniu Jednostki do inspekcji i audytów farmaceutycznych prowadzonych przez organy...
specjalista mid / senior / ekspert umowa o pracę pełny etat
561 dni
The main responsibility will Planning, execution, reporting, verifying the correctness of analytical tests commissioned to the Physico-Chemical Team Implementing new methods under transfer, validation and verification of analytical methods. Carring out and evaluation of QMS documentation....
Support the Microbiological Quality Control Team with knowledge and technical expertise in the field of microbiological techniques and analyzes. Ensure the performance of all microbiological tests and evaluation of related records. Ensure that all microbiological tests are performed in accordance...
Your responsibilities Drug Substance and Drug Product of biosimilars Review and maintain adherence to QC testing including validation, Specifications, and COA’s. Oversee any deviations or planned changes in QC and ensure authorization is in accordance with defined systems and relevant authorities....
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Medycyna, Farmacja i Służba zdrowia
specjalista (mid) / kierownik/koordynator kontrakt B2B pełny etat
