About this role
Job Description
- Buffer preparation for small and large-scale operations, IPQC operation of buffer and protein intermediate samples.
- CIP of chromatography systems, TFF systems and process vessels.
- SIP of TFF systems and process vessels.
- Operation of chromatography systems, TFF systems, Virus Filtration System, DS filtration for protein purification.
- Preparation, execution and maintenance of SOP’s, BPRs, qualification documents and other facility related documents.
- Co-ordinate with QC/QA teams on day-to-day activities of production operations.
- Review of executed BPR’s.
- Raw material and consumables inventory planning and maintenance.
- Operation, maintenance of sterile and decontamination autoclave.
- Deviation identification, initiation and investigation assistance for the facility related deviations.
Additional Job Responsibilities :
- Routine monitoring of facility and record maintenance e.g. temperature, humidity, differential pressure.
- Overall housekeeping management.
- To assist in facility validation in coordination with QA.
Work Experience
2-5 years of experience
Education
Graduation in Biotechnology or Biotechnology
## Competencies