Syngene Freshers Biotech Job Openings – Apply Online
Title: Executive
Date: 22 May 2025
Job Location: Bangalore
JOB DESCRIPTION
Designation: Executive
Job Location: Bangalore
Job Grade: 9
The Company
Syngene International Ltd. (BSE: 539268, NSE: SYNGENE, ISIN: INE398R01022), is an integrated research, development, and manufacturing solutions company serving the global pharmaceutical, biotechnology, nutrition, animal health, consumer goods, and specialty chemical sectors. Syngene’s 4500+ scientists offer both the skills and 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 1.9 Mn sq ft of specialist discovery, development and manufacturing facilities, as well as dedicated research facilities for Amgen, Baxter, Bristol-Myers Squibb and Herbalife, Syngene works with biotech companies pursuing leading edge science as well as multinationals including GSK and Merck KGaA.
Key Result Areas
Role-specific:
- Active involvement in all upstream manufacturing activities.
- Perform error free operation by eliminating operational gaps in advance.
- Active trouble shooting to minimize the various risks prior to execution and during execution.
- Initiate and process upstream deviations /investigations and closure.
- Pre -execution activity: Area and equipment readiness.
- Issuance of raw material /consumables and issuance batch records.
- Upstream process execution: Batch process operation /unit operation (including CIP, SIP and preparation upstream accessories), close monitoring of batch performance and data.
- Follow and practice on-line documentation all the time.
- Follow cGMP practices during the manufacturing activity and operations associated activities with QA, QC and EAM.
- Attend the training session of EHS, cGMP and HRD.
- Ensure process equipment’s/instruments are in Qualified in state.
- Verify PM, check the log books and ensure the clean room requirements in order to get line clearance from QA for batch execution.
- Active coordination with inter-depts. for sample submission, closure of documentation and timely execution and contribution for the assigned tasks.
- Perform on-line documentation, cGMP compliance in all the manufacturing activity, and timely closure of executed documents and batch records.
- Ensure the Quality system is followed in day today upstream operations. Identify the gaps in the system to improve.
- Active involvement in all upstream manufacturing activities.
- Perform error free operation by eliminating operational gaps in advance.
- Active trouble shooting to minimize the various risks prior to execution and during execution.
- Initiate and process upstream deviations /investigations and closure.
TECHNICAL /FUNCTIONAL SKILL:
- Expertise in Upstream unit operations (CHO based mammalian expression systems).
- Strong Hands on experience with SUB (Up to 2000 L scale)
- Exposure to handle of Bio-similar proteins and Mabs projects in cGMP area.
- Sound knowledge and awareness of GMP controls, Quality systems and regulatory aspects
- Experience on risk assessment tools and change management.
- Experience on the Equipment Qualification and commission aspects
Education and Experience
Education
Master’s degree in Pharmaceutical Sciences, Chemical Engineering, Biotechnology, or related field.
Industry Experience
Minimum 0-4 years of relevant practical experience in Upstream Manufacturing for biopharmaceuticals, specifically with CHO cell lines for monoclonal antibodies, fusion proteins, etc.
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