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 4-8 years of relavant experience. Education B.Tech in Biotechnology or Biotechnology Post Graduation in Biotechnology or Biotechnology Competencies 5. Result Orientation 1. Strategic Agility 2. Innovation & Creativity 3. Customer Centricity