#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 junior / mid / senior umowa o pracę pełny etat
638 dni
Your role As IT Application Support Specialist, you will be a part of Global IT team responsible for providing application support and management services for selected business applications supporting Polpharma Biologics development and manufacturing processes. This role will also be responsible for...
Twoje zadania Przygotowanie dokumentacji związanej z nawiązaniem i rozwiązaniem stosunku pracy; Aktualizowanie dokumentacji z ciągiem zatrudnienia pracowników; Wprowadzanie i kontrola poprawności i kompletności danych w systemie kadrowo-płacowym; Wprowadzanie dokumentów do akt osobowych i...
kierownik/koordynator / menedżer umowa o pracę pełny etat
640 dni
Your role Management of the Quality Control Bioassay team in the Quality Control department, cooperation with internal and external clients. Motivating employees and supporting them with knowledge and technical expertise in the field of biological techniques and analyzes. Preparation, review and...
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...
Role: Quality Compliance Senior Specialist assists Suppliers Qualification Manager in developing, implementing and supervising the operation of the Quality Management System. Support in the preparation of the Unit for pharmaceutical inspection and audits led by national and foreign authorities....
Role: In this position you will join a team of scientists focused on the development and characterization of downstream processes in R&D department. Your responsibilities: Planning and conducting lab studies for development, optimization and characterization of production purification processes,...
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...
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...
Your role: You will have the unique opportunity to participate in strengthening Quality Culture in the new biotechnological facility by partnering production, engineering, supply chain and quality control departments. You will be responsible for ensuring that GMP requirements are properly applied in...
Your responsibilities: Planning and execution of laboratory scale studies for the purpose of development and optimization of protein purification steps, including chromatography, filtration and membrane separations; Documented observations, analyzes of data, reporting of results and conclusions for...
specjalista mid / senior / ekspert umowa o pracę pełny etat
645 dni
Twoja rola Udział w projektach jakościowych dotyczących ciągłego doskonalenia farmaceutycznego systemu jakości w celu zapewnienia odpowiedniej jakości wytwarzanych produktów zgodnie z obowiązującymi przepisami i wytycznymi cGxP, cGMP, Prawa Farmaceutycznego, EMA, PIC/S, WHO, ISPE, PDA, EU...
specjalista mid / senior / ekspert umowa o pracę pełny etat
646 dni
Your responsibilities: Plan, manage, support and implement the quality assurance of equipment and systems (e.g. clean utilities and HVAC) qualification and sanitization/sterilization validation program consisting of entire system lifecycle (from URS, through implementation, changes to system...
kierownik/koordynator / menedżer umowa o pracę pełny etat
647 dni
Your responsibilities Shaping IT Policies and Procedures for Polpharma Biologics and cooperating within the global organization to harmonize processes; Evaluating the efficiency of IT controls and continuously improving them; Reporting risks or non-conformity issues; Driving an IT Audit readiness...
specjalista junior / mid / senior umowa o pracę pełny etat
647 dni
Your role The aim of the position is to supervise and maintain masterdata for Supply Chain, especially create, completeness and integrity of masterdata. Agree and create relevant procedures according to GMP and GDP. Supporting implementation of S4HANA. Your responsibilities Creation of material...
specjalista mid / senior / ekspert umowa o pracę pełny etat
647 dni
Your role Support organization in the implementation of the SAP S4/HANA, Optimizations and improvement in the specific area in SAP Materials Management, Purchasing, Warehousing from both operational and functional viewpoint. Your responsibilities Support organization in the implementation of the SAP...