2022-07-29 11:26:48

Production Technician DSP Biotech

CVMarket.lt klientas
2250 - 2660 €/m Gross

Job Description

3P Biopharmaceuticals is a leading European GMP Contract Manufacturing Organization (CMO) specialized in the process development and cGMP manufacture of Biologics and Cell Therapy products.

Custom manufacturing of Biologics from mammalian, yeast, and bacterial systems are developed from proof of concept to commercial stages being able to adapt to regulatory requirements for every phase. An integral and complete bioproduction service, with a wide range of related services, is offered by 3P Biopharmaceuticals.

Some of these services are the generation of expression systems, process development and optimization, generation and characterization of cell banks, formulation and stability studies among others.

 

We are looking for a Production Technician DSP Biotech to work in shifts.

 

Objetivo del puesto:

  • The successful candidate will join 3P Biopharmaceuticals, in Navarra Spain, as a Purification Technician in the Manufacturing Department.
  • The candidate will be expected to lead small teams in the Purification Manufacturing Process area for client projects, to ensure the biomolecules manufactured at 3P Biopharmaceuticals conform to GMP/regulatory expected criteria.
  • The candidate will manage a working sifth, and will be expected to provide know-how and technical input.

 

Capability in managing multiple projects in a fast paced environment with client interaction is expected.

 

Requirements

  • At least two years of experience in the biotech industry, working the DSP area (purification of recombinant proteins and monoclonal antibodies), from lysis to dosification of molecules.
  • Used to work in multidisciplinary teams with interaction with other departments of the company and external customers.
  • Experience in working in a project management basis.
  • Experience providing know-how in order to guarantee the right technology transfer as well as proposing improvements in quality, cost, performance, time and safety.
  • Strong practical experience using Chromatographic equipment ÄKTA Pilot and ÄKTA Ready at small, medium and large scale.
  • Performance of chromatographic methods using Unicorn 5 software, or upper version.
  • Experience in the preparation of documentation (SOPs, protocols, reports) to regulatory standards is essential.
  • Experience with relevant state-of-the art technologies is desirable.
  • Experience in managing method studies and teams is expected.
  • Familiarity with the manufacturing process (development) MAbs and/or biosimilars is desirable.
  • Familiarity with risk analysis and HAZOP.

 

Job location: Navarra (SPAIN)