USP Team Leader
Duchnice (pow. warszawski zachodni)

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 role

Participation in the production process of biotechnology products in accordance with the GMP principles and FDA requirements to obtain a product of the specified quality in the specification for registration. Participation in technology transfer in accordance with cGMP and internal regulations during the implementation of projects related to the introduction of internal and external biotechnology products. Managing of Operator's work during the shift.

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 Specialists;
  • 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;
  • Conducting the process and manufacturing documentation in accordance with the GMP principles and other internal requirements;
  • Reporting the progress of all work and statuses of tasks to the supervisor;
  • Cooperation in preparing reports on completed tasks;
  • Securing the workplace;
  • Organizing your and team's 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;
  • Leads the shift group and responsible of team members;
  • Determining training needs and delegating shift workers for trainings;
  • Conducting and participating in trainings.

If you have

  • Higher or secondary directional education;
  • 1-2 years work experience;
  • 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.

We offer

  • Private healthcare;
  • Life insurance;
  • Pension plan above national standards;
  • Relocation package;
  • Additional free day;
  • and moreā€¦
Join our Team!

Why you should work with us

Contact us
[email protected]