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Sun Pharmaceutical Ltd 

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Job Location: Baroda

Department : 
RBD Biotechnology-Protein Characterization

Grade : Executive/Sr Executive

Experience: 2-6 years

Qualification : 
M.SC/M.Tech-3 Biotechnology or Biochemistry

Brief Job Description

1) To develop LC-MS based methods for protein and peptide product characterization (2) To design and implement integrated strategies, linking appropriate chromatography and mass

spectrometry tools, to perform a qualitative and quantitative assessment of product related variants and Impurities. Develop and apply novel sample preparation with emphasis on LC-MS, CEX-MS, SEC-MS Characterization of innovator product batches sourced from different geographical region and preparation. of quality target profile

) Responsible for designing advance workflows such as multi-attribute methods for PTMs, sequence variants, qualitative and quantitative profiling of HCPs, Disulfide shuffling and bond analysis, cell culture metabolite analysis, glycan analysis etc

4) Preparation and review of method development reports (MDR) and analytical test procedures (ATF)

Technical/functional Skills:

Sound knowledge of analytical method development, qualification and structural and functional characterization of therapeutic proteins.

Experience of bio-similarity assessment of biologics for regulated market is desirable,

Experience of analytical development for monoclonal antibodies and fusion proteins and peptide is highly desirable

1) To develop HPLC based methods for protein and peptide products.

2) to design and implement integrated strategies, linking appropriate analytical tools, to perform a qualitative and quantitative assessment of product related variants and impurities. Develop and apply novel sample preparation with emphasis on RP-HPLC, SEC-HPLC, CEX-HPLC..etc

Department ;R&D Biotechnology- Analytical Development (in Process)

Grade :Executive/Sc. Executive

Experience :5-9 years

Qualification ;M.SC/M.Tech- Biotechnology or Biochemistry

Brief Job Description
3) Responsible for designing advance workflows to measure & characterize process related impurities at different stages of product development such as Host cell protein (HCPs), Host Cell DNA (HCD) & Leachable

4) Responsible for preparation and review of method development reports (MDR) and analytical test procedures (ATP)

Technical/functional Skills:

Sound knowledge of analytical methed development, qualification.

Experience in biosimilar development for regulated market is desirable.

Experience of analytical development for monoclonal antibodies and peptide is highly desirable.

Please send your resume to: HR.Tandalja@sunpharma.com

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  • Interview Questions [Result oriented collection] 
1️⃣ Technical interview Questions
2️⃣ Centrifugal Pump Interview Questions
3️⃣ Chemical Reactor Related interview Questions
4️⃣ Distillation interview Questions
5️⃣ Pumps Interview Questions
6️⃣ Valves Interview Questions
7️⃣ DCS Distributed Control System Interview Questions
8️⃣ Heat exchangers Interview Questions
9️⃣ Safety Interview Questions
1️⃣0️⃣ Pharmaceutical Interview Questions
1️⃣1️⃣ HR Interview Question

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