Kemwell Biopharma Pvt Ltd, is a 100% customer-oriented company with deep expertise in contract development and manufacturing services for pharmaceutical products. We bring over 30 years of experience. Headquartered in Bangalore, India, Kemwell has four facilities in India and one in Sweden, catering to 5 of the top 10 Pharma companies of the world. Throughout our journey, we have maintained our pure-play status as a 100% contract services provider without foraying into any branded products of our own. This has strengthened our core value and work culture that the "Customer Comes First Always." This commitment to respecting IP rights and working collaboratively with our customers has won the confidence of the top Pharma companies of the world, with companies such as GSK and Pfizer trusting Kemwell to supply some of their highest-selling products for decades. Today, Kemwell services companies such as Allergan, Bayer, GSK, J&J, Pfizer and Novartis, manufacturing 4 of the top 10 brands sold in India and employing over 1000 people worldwide.
Job Title: Jr.executive/ Executive - QC HPLC for Biologics
Qualification: B.sc/M.Sc Bio-Chemistry, Microbiology/ Life Science
Experience: 0-4 years
Job Description:
- To perform all the In process, Drug substance, Drug product (Release and stability) related sample analysis in the HPLC section along with necessary documentation with required and defined level of compliance.
- To prepare SOPs, STPs, specifications and protocols related to HPLC section.
- To prepare Qualification Protocols (IQ, OQ, PQ), execution and preparation of report for equipment related to HPLC sections.
- To execute all activities related to Stability Studies e.g. protocol preparation, charging of samples, analysis, report preparation, trend analysis etc. for all products at different stages.
- To execute all activities related to Analytical Method Validation and Method optimization e.g. protocol preparation, analysis and report preparation.
- To ensure proper usage of equipment, cleaning, calibration and verification as per schedule and to ensure concurrent recording of data in respective formats.
- To maintain inventory of all consumable used in HPLC section.
- To attend all GMP related trainings and QC and QA SOP related trainings.
How to Apply:
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