About this role
Job Description
- Act as shift supervisor, lead, train and mentor the downstream team.
- 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.
- Monitor key process parameters.
- 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.
- Preparation of GMP documents like- Qualification and validation protocols and other process or facility related documents for media preparation and cell culture operations.
- Work Experience 3-7 YEARS OF EXPERIENCE Education Masters in Biotechnology B.Tech in Biotechnology Competencies
- 1. Strategic Agility
- 2. Innovation & Creativity Building a Safe Environment