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.
Your role: As IT Security and Compliance Manager you will define and deliver the objectives within the Information Security strategy and further enhance a security program that identifies and addresses compliance, security and privacy risks as well as security requirements. You will be working...
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: Participating in the project related to the launch of a new laboratory at the plant on biotechnology, Developing new and updating existing documentation (instructions, procedures, sampling plans, specifications, certificates, risk assessment), Cooperation with...
Your responsibilities: Participating in the project related to the launch of a new laboratory at the plant on biotechnology, Developing new and updating existing documentation (instructions, procedures, sampling plans, specifications, certificates, risk assessment), Cooperation with...
Your responsibilities: Participating in the project related to the launch of a new laboratory at the plant on biotechnology, Sample management (registration, splitting product samples, distribution samples for testing), Developing new and updating existing documentation (instructions, procedures,...
Twoja rola: Jako Specjalista ds. serwisów w Dziale Inżynieringu twoją rolą będzie koordynowanie i nadzorowanie prac serwisowych i naprawczych oraz prac konserwacyjnych harmonogramowanych w ramach planu prewencyjnego.
Your role: The Biotech Producon Scheduler is responsible for providing producon planning, managing producon inventory, organizing and coordinang acvies of producon support funcons to effecvely sustain product transformaon operaons. The Biotech Producon Scheduler manages the requirements and...
Your role: In this role you will be responsible for facilitation of sharing of resources, methodologies, tools and techniques. You will ensure that company standards, procedures and practices are being followed. You will also be tasked with management of single-source of truth software tool that...
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...
Your role: We are looking for a Drug Product Specialist to join our new department in Gdańsk. In this position you will work on the production processes, to make sure they are in line with the quality requirements and company procedures. You will participate in range of activities in accordance...
Your role: In this role you will be responsible for all activities related to Upstream process development and USP laboratory operation based on solid scientific and engineering knowledge. You will be a mentor for more junior team members as well.
Your role: As an IT Application Support Specialist, you will be implementing, troubleshooting and maintaining service quality for selected applications to support Polpharma Biologics development and manufacturing processes. It is an exciting opportunity to join newly establishing Application...
Rola: Weźmiesz udział w procesie wytwarzania produktów biotechnologicznych zgodnie z zasadami GMP oraz wymogami FDA w celu otrzymania produktu o jakości zadanej w specyfikacji.
Twoje zadania: Wykonywanie operacji procesowych, po uprzednim instruktażu i w zgodzie z zasadami GMP; Analizowanie uzyskanych wyników procesowych pod kątem zgodności w dokumentacją technologiczną oraz wewnętrznymi wymaganiami; Udział w transferze technologii, charakterystyce procesu oraz...
od 251 do 500 prac.
