Syngene International is hiring for the position of Associate – Operations in its Development Manufacturing and Commercial department in Bangalore, Karnataka. The role involves manufacturing operations, equipment monitoring, batch documentation, and compliance with current Good Manufacturing Practices (cGMP), environmental health and safety (EHS) requirements, and data integrity policies.
Job Details
| Particulars | Details |
|---|---|
| Company | Syngene |
| Job Title | Associate – Operations |
| Department | Development Manufacturing and Commercial |
| Division | Development Services |
| Job Location | Bangalore, Karnataka – 560099 |
| Qualification | B.Sc. in Organic Chemistry |
| Experience | 1–2 years |
| Job Posting Date | 17 October 2026 |
Position
Associate – Operations
The selected candidate will support manufacturing activities, including batch execution, filtration, workup, drying, product handling, and packaging, while maintaining compliance with manufacturing procedures, quality standards, and safety protocols.
Job Responsibilities
- Carry out manufacturing operations in compliance with cGMP, Good Documentation Practices (GDP), and data integrity policies.
- Monitor shift activities and production operations while ensuring facility and equipment readiness.
- Operate, monitor, and maintain high-potency active pharmaceutical ingredient (HPAPI) manufacturing processes in accordance with containment protocols and EHS requirements.
- Coordinate the preparation of production documents, including SOPs, EOPs, ECCs, BMRs, and PDRs.
- Verify equipment readiness, cleanliness, and raw material requirements before manufacturing activities.
- Receive and verify raw and packing materials against batch records and issue slips, ensuring appropriate labelling.
- Maintain contemporaneous batch documentation in accordance with ALCOA data integrity principles.
- Perform batch charging, filtration, workup, drying, product handling, and packaging activities as per batch manufacturing records.
- Operate the Distributed Control System (DCS) according to batch manufacturing records and update relevant documentation.
- Maintain equipment logbooks, daily checklists, and online documents and annexures.
- Ensure the availability of manufacturing consumables, including filter cloths, sample bottles, labels, and filter cartridges.
- Report deviations and variations to the supervisor and support non-conformance reporting and corrective action implementation.
- Coordinate the checking and disposal of mother liquor, aqueous layers, spent solvents, and spent solids with relevant personnel.
- Submit samples to Quality Control (QC) and follow up on analytical reports.
- Take charge of the previous shift after verifying reaction conditions, equipment cleanliness, raw materials, and solvent availability.
- Follow HPAPI containment procedures, permit-to-work systems, safe operating procedures, and other EHS requirements.
- Participate in risk assessments, emergency response drills, safety initiatives, and mandatory training.
- Coordinate with senior management to support effective manufacturing operations.
Eligibility and Qualifications
Candidates must meet the following requirements:
- Educational Qualification: B.Sc. in Organic Chemistry.
- Experience: 1–2 years of experience in manufacturing operations.
Required Skills and Knowledge
The job responsibilities require knowledge or working capability in the following areas:
- Pharmaceutical or chemical manufacturing operations
- Current Good Manufacturing Practices (cGMP)
- Good Documentation Practices (GDP) and ALCOA data integrity principles
- Batch Manufacturing Records (BMR) and production documentation
- Equipment readiness and manufacturing process monitoring
- HPAPI containment and occupational exposure control
- Distributed Control System (DCS) operations
- Environmental health and safety (EHS) compliance
- Deviation reporting and corrective action implementation
- Coordination with Quality Control and manufacturing teams
