Manufacturing Purification Technician

División

Engineering

Empresa

-

Descripción

The candidate will be expected to lead small teams in the Purification Manufacturing Process area for client projects, to ensure the biomolecules manufactured at the company conform to GMP/regulatory expected criteria.

The candidate will manage a working sift, 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 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.
• Familiarity with the manufacturing process (development) MAbs and/or biosimilars is desirable.
• Familiarity with risk analysis and HAZOP.
Other requirements:
- Fluent in English.
- Willing to relocate to Northern Spain

Lugar de trabajo:

Navarra

Disponibilidad:

Selección directa

Jornada laboral:

Full Time

Fecha de publicación:

14/03/2019

Código de la oferta:

20128

Visitas a esta oferta:

2

Oficina / Departamento:

Experis ICT Madrid

Vacantes:

1
 
 

Manufacturing Purification Technician

Navarra
Selección directa
Full Time
14/03/2019
20128
2
Experis ICT Madrid
1

Sector

Engineering

Empresa

-

Descripción

The candidate will be expected to lead small teams in the Purification Manufacturing Process area for client projects, to ensure the biomolecules manufactured at the company conform to GMP/regulatory expected criteria.

The candidate will manage a working sift, 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 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.
• Familiarity with the manufacturing process (development) MAbs and/or biosimilars is desirable.
• Familiarity with risk analysis and HAZOP.
Other requirements:
- Fluent in English.
- Willing to relocate to Northern Spain