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Manufacturing Specialist
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#549287
Full Time
Job Description
Plasmid Manufacturing Vapi I Micro CRISPR Pvt Ltd
Upstream Process
• To oversee and manage day-to- production operation during assigned shift, ensuring smooth workflow and adherence to production schedule.
• To ensure the batch processed as per compliance
• As an Upstream expert you will be handling Fermenters up to 100L, Continuous centrifuge, TFF System, Process vessel, Double Door Autoclave, DHS, Filter integrity and all critical instruments.
• Responsible for preparation of media and buffers for fermentation and early stage downstream process.
• Manage inoculations and transfer of culture with strict aseptic technique
• Perform and supervise the CIP and SIP of the equipments.
• Conducting regular checks to ensure production, quality, Process consistency and regulatory adherence.
• Liaise with QA to address deviation, non conformances and ensure the release high quality product.
• Preparation of GMP documents like MPCR, BPCR, SOP, Protocol and Validation and revalidation of critical equipments.
• Develop and implement the shift plan to ensure optimal utilization of available person.
• To perform the job assigned by supervisor or HOD.
Downstream Process
• To oversee and manage day-to- production operation during assigned shift, ensuring smooth workflow and adherence to production schedule.
• To ensure the batch processed as per compliance
• As a Downstream expert you will be handling different types of Chromatography (ion exchange, hydrophobic interaction etc), TFF System, Process vessel, double door autoclave, DHS, Filter integrity and all critical instruments.
• Preparation of reagent and buffer required for various purification steps.
• Conducting regular checks to ensure production, quality, and Process consistency and regulatory adherence.
• Perform and supervise the CIP and SIP of the equipments.
• Preparation of GMP document like MPCR, BPCR, SOP, Protocol etc and Liaise with QA to address deviation, non conformances and ensure the release high quality product.
• Responsible validation and revalidation of all critical equipments of the area.
• Develop and implement the shift plan to ensure optimal utilization of available person.
• To perform the job assigned by supervisor or HOD.
Interested candidates may share their updated resume at sanjaykumar.aahir@microcrispr.com
To learn more about our company and our groundbreaking work in this field, please visit:
Micro CRISPR
Meril Life Sciences (Parent Company)
Looking forward to hearing from you!
Upstream Process
• To oversee and manage day-to- production operation during assigned shift, ensuring smooth workflow and adherence to production schedule.
• To ensure the batch processed as per compliance
• As an Upstream expert you will be handling Fermenters up to 100L, Continuous centrifuge, TFF System, Process vessel, Double Door Autoclave, DHS, Filter integrity and all critical instruments.
• Responsible for preparation of media and buffers for fermentation and early stage downstream process.
• Manage inoculations and transfer of culture with strict aseptic technique
• Perform and supervise the CIP and SIP of the equipments.
• Conducting regular checks to ensure production, quality, Process consistency and regulatory adherence.
• Liaise with QA to address deviation, non conformances and ensure the release high quality product.
• Preparation of GMP documents like MPCR, BPCR, SOP, Protocol and Validation and revalidation of critical equipments.
• Develop and implement the shift plan to ensure optimal utilization of available person.
• To perform the job assigned by supervisor or HOD.
Downstream Process
• To oversee and manage day-to- production operation during assigned shift, ensuring smooth workflow and adherence to production schedule.
• To ensure the batch processed as per compliance
• As a Downstream expert you will be handling different types of Chromatography (ion exchange, hydrophobic interaction etc), TFF System, Process vessel, double door autoclave, DHS, Filter integrity and all critical instruments.
• Preparation of reagent and buffer required for various purification steps.
• Conducting regular checks to ensure production, quality, and Process consistency and regulatory adherence.
• Perform and supervise the CIP and SIP of the equipments.
• Preparation of GMP document like MPCR, BPCR, SOP, Protocol etc and Liaise with QA to address deviation, non conformances and ensure the release high quality product.
• Responsible validation and revalidation of all critical equipments of the area.
• Develop and implement the shift plan to ensure optimal utilization of available person.
• To perform the job assigned by supervisor or HOD.
Interested candidates may share their updated resume at sanjaykumar.aahir@microcrispr.com
To learn more about our company and our groundbreaking work in this field, please visit:
Micro CRISPR
Meril Life Sciences (Parent Company)
Looking forward to hearing from you!
