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 trouble shooting, 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.
• Trouble shooting 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-Biotechnolgy/M.tech Biotechnology

Industry Experience

2 to 5 years of relevant experience