BioProcess Technician

at  Recipharm

GenIbet is a cGMP biopharmaceutical CDMO - Contract Development Manufacturing Organization - offering highly specialized microbial, cell culture and viral process development and cGMP manufacturing services to research groups, biotech and pharma companies.
GenIbet’s core activity is the manufacture and supply of materials for use in early-stage drug development, pre-clinical studies and cGMP manufacturing for clinical trials and commercial.

Requirments:

• Participate in the preparation of raw materials, and solutions using specific techniques involved in each operation, according to the manufacturing process set (BPR), with a view to proper use in the production process;
• Participate and coordinate the operation, of the equipment needed to carry out the different production operations in accordance with the procedures laid down.
• Support the execution of the process of fermentation, cell culture, viral production and purification, in accordance with the procedures laid down, ensuring the attainment of the targets originally planned and with high quality standards;
• Split/separate the product in a suitable packaging, and according to the defined in BPR, for other laboratory tests, clinical, toxicological, among others, according to the requested by the client;
• Support the Investigation and development of processes under way in GenIbet, such as optimization and increased scale of operations of fermentation, cell culture, viral production and purification, in accordance with the requirements of the customer and in strict compliance with the GMPs;
• Report to Team Leader, the identified deficiencies during the production process;
• Develop new procedures and improve existing procedures for the constant improvement of the GenIbet’s quality system, processes and support activities.

REQUIRED EXPERIENCE AND EDUCATION

• Minimum 3 years of work experience in biopharmaceuticals production and purification, preferably in GMP production environment.
• MSc in Biotechnology, Chemical/Biochemical Engineering, Pharmaceutical Sciences, Biochemistry or related sciences.

CORE COMPETENCIES AND REQUIREMENTS :

• Technical-scientific domain of bioprocesses
• Good Manufacturing Practice
• Production and Purification of biopharmaceuticals
• Availability to work in shifts
• Domain of English language with at least advanced level
• Good team spirit and good communication skills
  Send your CV to Recursos.humanos@genibet.com
  Be part of a team that is changing the future in the field of Biologics with innovation, passion and excellence. We look forward to receiving your application

Please refer the Job description for details