Shift Leader USP

Shift Leader USP
Boost your career with us
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.
Join our Team!
Why you should work with us
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