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
B.Tech in Biotechnology or Biotechnology
Post Graduation in Biotechnology or Biotechnology
Competencies
-
Strategic Agility
-
Developing Talent
-
Result Orientation