BTech Biotech Job at Syngene – MTech Apply Online
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
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