3 Downstream Production Jobs

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3.0 - 8.0 years

4 - 9 Lacs

thane

Work from Office

Role & responsibilities Operate and monitor Tangential Flow Filtration (TFF) systems including membrane integrity checks (water permeability, pressure-hold, bubble point tests). Perform Ultrafiltration (UF) and Diafiltration (DF) for protein concentration and buffer exchange. Conduct Ion Exchange Chromatography for protein purification based on charge properties. Independently handle AKTA chromatography systems , BPG glass columns , and SS vessels (500L capacity) . Execute RP-HPLC analysis for product quality and purity. Maintain and follow QMS documentation including Change Control , Deviation , SOPs , and Batch Manufacturing Records (BMR) . Monitor Transmembrane Pressure (TMP) to ensure co...

Posted 1 month ago

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2.0 - 6.0 years

0 Lacs

gujarat

On-site

Fishfa Biogenics is offering opportunities for professionals in various functions such as Operations, Quality, Sales & Marketing, Human Resources, Finance, Business Development, Logistics, EHS, and Regulatory Affairs. We are currently looking for individuals to join our team in the API Bio-processes department for Column purification / Solvent extraction and Downstream Production. Position: Operator Experience: 2-5 Years Qualification: ITI or equivalent Vacancy: 2 positions At Fishfa Biogenics, we believe in fostering a work environment that encourages new ideas and provides individuals with the freedom to explore. We value and reward employees who contribute towards achieving our company's ...

Posted 3 months ago

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2.0 - 7.0 years

4 - 9 Lacs

Hyderabad

Work from Office

Key Responsibilities: Execute routine downstream operations including chromatography (affinity, ion exchange, HIC), filtration techniques (TFF, UF, DF, NF), buffer preparation, and formulation of mammalian cell culture-derived products. Maintain accurate documentation including batch records, deviation reports, SOPs & other QMS elements. Support scale-up and tech transfer from lab to pilot/production scale. Ensure strict compliance with cGMP and safety protocols. Collaborate with QA/QC, maintenance, and engineering teams for smooth operations. Troubleshoot process deviations and contribute to root cause analysis and CAPA implementation.

Posted 6 months ago

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