Junior Executive Jobs at Syngene | M Pharm Candidates Apply Now
Are you looking to build your career in biologics and pharmaceutical manufacturing? Syngene International Ltd. is hiring a Jr. Executive – Manufacturing Services at its Bangalore facility. This role provides an excellent opportunity to gain hands-on expertise in downstream processing, biologics operations, and compliance, while working in a world-class research and manufacturing environment.
About the Company
Syngene International Ltd. (BSE: 539268, NSE: SYNGENE) is a leading integrated research, development, and manufacturing solutions provider serving the pharmaceutical, biotechnology, nutrition, animal health, consumer goods, and specialty chemical industries worldwide. With over 4,500 scientists and 1.9 million sq. ft. of state-of-the-art facilities, Syngene partners with top global innovators, including Amgen, Baxter, Bristol-Myers Squibb, Herbalife, GSK, and Merck KGaA. The company is known for delivering cutting-edge science, robust data management, IP security, and high-quality manufacturing to accelerate innovation and bring life-saving solutions to market faster.
Job Details
Job Opportunity: Jr. Executive – Manufacturing Services
Location: Bangalore, KA, IN, 560099
Job Grade: Associate
Education: Master’s / Bachelor’s in Pharmacy or Pharmaceutical Sciences.
Experience: Minimum 1–4 years of relevant experience in mAbs downstream process.
Key Responsibilities
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Maintain aseptic behavior inside the Biologics operations facility.
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Perform downstream activities including assembly preparation, buffer preparation, filtration, chromatography, and TFF operations.
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Operate and clean downstream equipment as per SOPs.
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Monitor processes, maintain quality records, and perform in-process sampling.
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Prepare, review, and update operation-related documents and protocols.
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Ensure readiness of facilities for inspections and audits.
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Coordinate with QA for line clearances and support error-free batch execution.
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Support shipment of samples/final products per packing and dispatch records.
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Report deviations, nonconformities, and ensure timely closure of work orders.
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Participate in training, audits, and compliance with cGMP, EHS, and data integrity standards.
Other Competencies
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Strong knowledge of cGMP, GDP, EHSS practices, and regulatory compliance.
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Ability to manage documentation, deviations, CAPA, and change controls.
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Adherence to organizational safety, quality, and data integrity standards.
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Effective team collaboration and reporting discipline.
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