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
3-8 years of mammalian manufacturing experience
Education
Graduation in Biotechnology or Biotechnology
B.Tech in Biotechnology or Biotechnology
Competencies
1. Strategic Agility
2. Innovation & Creativity
3. Customer Centricity
4. Developing Talent

Skills Required