Dołącz do zespołu ponad 1300 specjalistów produkujących zaawansowane leki biologiczne, które poprawiają jakość życia pacjentów na całym świecie.
Bazując na doświadczeniu Polpharma Biologics, Rezon Bio działa jako partner CDMO (Contract Development and Manufacturing Organization).
Dzięki nowoczesnym centrombiotechnologicznym w Gdańsku i Warszawie-Duchnicach oferujemy szeroki wachlarz możliwości karierowych w obszarach naukowych, technicznych i biznesowych.
Responsibilities As part of the Fiz-Chem Team, planning and coordinating and testing of final products, intermediate products, raw materials and clean media. Periodical replacing of team manager. Development of quality system documents. Participation in the qualification of control and measurement...
starszy specjalista (senior) / ekspert umowa o pracę pełny etat rekrutacja online aplikuj szybkoaplikuj bez CV
1022 dni
About the role As a QA Senior Specialist you will work across different units within the organization. In this role, you will monitor and track changes across the site. Moreover, you will also proactively identify and resolve quality issues to ensure compliance and high productivity. You will be...
Your role Participation in manufacture of biotechnology products in accordance with cGMP principles and FDA and other regulatory agencies requirements to obtain a product of specified quality in the specification. Improving and optimizing production processes by proposing changes and implementing...
specjalista junior / mid / senior umowa o pracę pełny etat
1028 dni
Your role As an 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, manufacturing and quality processes. This is an exciting...
specjalista junior / mid / senior umowa o pracę pełny etat
1028 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
1030 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
1035 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...
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