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DSP MSAT Specialist (55892)

Requisition ID 55892

Posted 04/15/2024 – India

Designation: Associate Scientist, Biopharmaceutical Development(Downstream MSAT)

Job Location: Bengaluru, India

Reporting to: Principal Scientist, Biopharmaceutical Development

Job Grade: 8-I

Operating Unit: Biopharmaceutical Development

Department: Biopharmaceutical Development

The Company

Syngene International Ltd. (BSE: 539268, NSE: SYNGENE, ISIN: INE398R01022), is an integrated research, development, and manufacturing services company serving the global pharmaceutical, biotechnology, nutrition, animal health, consumer goods, and specialty chemical sectors. Syngene’s 4500+ scientists offer both skills and the capacity to deliver great science, robust data management and IP security and quality manufacturing, at speed, to improve time-to-market and lower the cost of innovation. With a combination of dedicated research facilities for Amgen, Baxter, Bristol-Myers Squibb, and Herbalife, as well as 1.9 Mn sq ft of specialist discovery, development, and manufacturing facilities, Syngene works with biotech companies pursuing leading-edge science as well as multinationals including GSK and Merck KGaA.

The Role

To perform activities related to MSAT function for technology transfer for downstream (microbial/mammalian culture), scale up, deviation investigation, process troubleshooting, technical report writing as per guidance and other documents available in Syngene.

Key Result Areas

Role-specific:

  • Execute and monitor downstream experiments as per the requirement, data analysis and interpretation of data along with feedback to manufacturing team/PD team.
  • Perform internal and external upstream technology transfer initiatives.
  • Preparation, review of TTD and BMR review.
  • Participate in planned and unplanned deviation investigation and perform/support related experimentation.
  • Understand the facility constraint and perform gap assessment, shop floor support for technology transfer and scale up related activities.
  • Author technical reports. Documentation includes gap analysis, risk assessment, statistical data analysis and other related technical reports.
  • Data collection/capturing, monitoring, trending and analyzing the data from cGMP campaign and authoring of summary reports.
  • Troubleshooting of process/product-related concerns.
  • Represent DSP technical team for client interactions and telecoms. Coordination with cross-functional teams.
  • Possess the knowledge and exposure to Environment, Health, Safety, and Sustainability (EHSS) practices.
  • Follow Environment, Health, Safety, and Sustainability (EHSS) requirements at all times in the workplace ensuring individual and lab/plant safety.
  • Attend training on Environment, Health, Safety, and Sustainability (EHSS).

Education and Experience

Education:

B.Tech-Biotechnology/M.tech Biotechnology

Industry Experience:

2 to 5 years of relevant experience

APPLY ONLINE HERE

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