Polpharma Biologics is a state-of-the-art biological R&D and manufacturing facility, one of the most modern in Europe. We have a fantastic, international team of experienced experts and dynamic young scientists with common goals and values. Biotechnology is our passion.
Together we develop medicines, offering a new hope to patients suffering from serious diseases. We create a passionate and friendly workplace environment. Join us!
Your responsibilities:
Performing procedural operations after prior preparation and in accordance with the GMP rules;
Analysing the obtained process results in terms of compliance in the technological documentation and internal requirements;
Participation in technology transfer, process characteristics and process validation in cooperation with Team Specialist;
Ongoing delivery to the supervisor and / or relevant persons of reports and all documentation necessary to evaluate the process;
Informing the immediate supervisor about any irregularities in the process, documentation, status of tasks performed and decisions taken;
Monitoring the production process of biotechnology products in accordance with the technological documentation;
Reporting the progress of all work and statuses of tasks to the supervisor;
Worthy of representing the company;
Cooperation in preparing reports on completed tasks;
Securing the workplace;
Organizing your and teams work in order to make the most effective use of working time and performance of tasks;
Cooperation with all Department teams and all other groups both within the company and in the Polpharma group;
Support in developing procedures;
Support in the development of equipment qualification documentation, conducting qualification and / or participation in the qualifying;
Preparation of equipment manuals and training;
Leading the shift group and responsible of team members;
Executing supervisors instructions;
Determining training needs and delegating shift workers for trainings;
Conducting and participating in trainings.
If you have:
Experience in laboratory work and the ability to handle basic laboratory / analytical equipment;
Good knowledge of requirements and experience in work according to cGMP;
Experience in keeping and review GMP production documentation;
Good knowledge of aseptic techniques and Single Use Technology used in biopharmaceutical production;
Knowledge of the basics of production of biotechnological drugs;
Knowledge of MS Office;
Good work organization, individual problem solving, good communication, team cooperation skills and being open for new tasks are required;
Good speaking and writing English skills;
Experience in managing people and planning of the team work.
