Senior DSP Process Specialist
Duchnice
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!
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
For our Technical Operations Department we are looking for a Senior DSP Process Specialist. On this position 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 biotechnology products in accordance with GMP principles and FDA requirements.
Your responsibilities
- Running and monitoring the manufacturing process of biotechnology production according to GMP requirements, technological documentation and other internal requirements.
- Coordination of production team in aim of effective resources utilization, conducting the trainings.
- Supervision over schedules related to the preparation of GMP documentation in the Production Department - e.g. procedures, qualification documents, etc.
- Supervision and issuance of system documentation in the Production Department.
- Elaboration, verification design and qualification documentation. Participation during equipment and systems qualification.
- Elaboration of SOPs and manuals (including manuals to equipment).
- Documentation preparation according GMP rules and internal company requirements.
- Participation in technology transfer and process validation in cooperation with MSAT and external Clients.
- Close cooperation with the MSAT and Quality Department.
- Monitoring the progress of preparation for inspections and audits (external and internal)
If you have:
- Higher education in Biotechnology or Pharmacy or any related field
- At least 5 years' experience in biotechnological or pharmaceutical industry.
- Good knowledge of cGMP and FDA requirements.
- Experience within protein purification processes. Knowledge of filtration and chromatography techniques.
- Excellent knowledge of Single Use Technology used in biopharmaceutical production will be additional advantage.
- Experience in work with recombinant proteins in production scale will be additional advantage.
- Understanding of protein chemistry and interactions related with that.
- Experience in keeping and reviewing process and project documentation according to GMP requirements.
- Fluent English and Polish
- Availability to work on shifts
- Good work organization, individual problem solving, good communication, team cooperation skills and being open for new tasks are required