#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.
Your responsibilities Commercial representative in the Cross-functional Program Team Meetings (XPT) providing key strategic market insights (biosimilar and disease area competition). Provide patient, market and competitive understanding identifying trends and opportunities WW. Provide market input...
Your role: As a member of our Technical Operations department you will participate in technology transfer in accordance with cGMP and internal regulations during the implementation of projects related to the introduction of new biotechnology products. You will participate in manufacturing of...
starszy specjalista (senior) umowa o pracę pełny etat
1207 dni
Role: At this position you will join our Team of specialists dedicated to support of Quality Control activities at Polpharma Biologics. Your main tasks will be to take care of Quality related documentation and its proper processing within our Quality Management Systems.
Your role: Management of the CC1 supporting team in the Quality Operations Department. Motivating employees and supporting them with substantive knowledge and expertise in the field of regulatory provisions. To assist Quality Operations Head in developing, implementing and supervising the operation...
Your role: Management of the DP1, Quality Control and Supply Chain (Shared Support) supporting team in the Quality Operations Department. Motivating employees and supporting them with substantive knowledge and expertise in the field of regulatory provisions. To assist Quality Operations Head in...
Twoje zadania: Wykonywanie operacji procesowych, po uprzednim instruktażu i w zgodzie z zasadami GMP. Analizowanie uzyskanych wyników procesowych pod kątem zgodności w dokumentacją techno-logiczną oraz wewnętrznymi wymaganiami. Udział w transferze technologii, charakterystyce procesu oraz...
Your role: Key element of the role is to assure ongoing compliance of production, quality control and warehouse activities, facilities and processes with quality and industry regulatory requirements and internal quality standards, policies, and procedures.
Your responsibilities Support organization in the implementation of the SAP S4/HANA; Optimizations and improvement in the specific area in SAP MM/eWM from the both operational and functional viewpoint; Support of End Users and Functional Consultants in SAP System maintenance; Take part in Master...
Your responsibilities Support organization in the implementation of the SAP S4/HANA; Optimizations and improvement in the specific area in SAP Production planning from the both operational and functional viewpoint; Support of End Users and Functional Consultants in SAP System maintenance; Take part...
Your responsibilities Serving as Subject Mater expert for Cleaning and Process Validation according to cGMP and FDA requirements; Review and approve validation documentation and provide guidance to site staff on cGxP requirements for cleaning and process validation; Performing and approving the GxP...
Your role As Corporate Development Manager you will manage and update business cases and collect market intelligence on competitive programs. You will also support our leadership team with strategic and ad-hoc analyses and work closely with the Finance team on long-term financial forecasts. Finally,...
Your role: Documentation Specialist’s role is to participate in the process of supervision, control and revision of the quality documentation related to the activities carried out in the Microbiological Production Department, in accordance with the GMP rules and FDA requirements.
Twoja rola: Odpowiedzialność za przygotowania specyfikacji, zakup, kwalifikację urządzeń produkcyjnych. Udział w procesie transferu technologii zgodnie z zasadami GMP oraz wewnętrznymi podczas prowadzenia projektów związanych z wprowadzeniem nowych produktów biotechnologicznych. Udział w...