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.
specjalista junior / mid / senior umowa o pracę pełny etat
1607 dni
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...
Your responsibilities: Administrate automation systems in Polpharma Biologics in Gdańsk; Support Automation systems’ design and modifications within investment projects; Diagnose and solve issues in automation systems; Make automation systems working as intended by cooperation with Production,...
Your role: As a Senior Automation Specialist you will be a part of our Automation Department, a team of experienced engineers, technical subject matter experts and administrators of all automated systems in our organization. The Automation Department designs, develops, builds, manages operations and...
specjalista junior / mid / senior umowa o pracę pełny etat
1608 dni
Your role: The Computer Systems Validation Senior Specialist will plan, manage, and implement the validation of Biotech equipment Computer Systems. He will act as the validation owner for the group of systems they are selected for. The candidate will work with the user and the Engineer to define and...
specjalista junior / mid / senior umowa o pracę pełny etat
1608 dni
Your role: The Equipment Validation Senior Specialist will plan, manage, implement the validation of Biotech Production equipment and act as the validation owner for the group of systems they are selected for. The candidate will work with the User and the Engineer to define and execute the program...
Twoje zadania: Samodzielne prowadzenie prac związanych z opracowywaniem, kwalifikacją oraz walidacją nowych metod analitycznych lub modyfikacją istniejących metod dla farmakologicznie aktywnych cząstek biologicznych oraz produktu leczniczego celem rejestracji, badań przedklinicznych i...
Your responsibilities: Developing and reviewing Quality System documentation; Participation in continuous improvement of existing Quality System; Providing guidance regarding current trends in FDA/EMA regulations (incl. upcoming requirements and lessons learnt from); Operational support in...
Your role: In this role, you will have an opportunity to take part in the whole life cycle of biopharmaceutical product development and production. You will be responsible for risk assessments, investigations related to deviations, proper documentation management, and preparations for audits and...
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...
Twoje zadania: Jako Stażysta w Dziale Zasobów Ludzkich wesprzesz nasz zespół w codziennych aktywnościach związanych z różnorodnymi procesami HR. Zdobędziesz wiedzę z zakresu przygotowania procesu onboardingu dla nowych pracowników, tworzenia opisów stanowisk, organizacji Welcome Days, a...
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 responsibilities: Administration of clustered Windows server environment including RDS and SQL; Administration of Citrix farm; Supporting Infrastructure operations as 3rd line of support; Taking care of updates, ensuring high availability and performance of infrastructure environment and...