Laurus Bio
Assistant Manager / Deputy Manager - Downstream Processing (DSP)
Skills
1 month ago
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Important information
Contract type:
Permanent
Salary:
₹900,000 – ₹1,200,000 / year
Location:
Andra, Andhra Pradesh 535273, India
Work mode:
Onsite
Published on:
9 September 2026
What they need
Job Summary:
The Production Assistant Manager / Deputy Manager DSP is responsible for leading all downstream processing operations during the assigned shift to ensure consistent, efficient, and GMP-compliant production of biological products (e.g., monoclonal antibodies, vaccines, recombinant proteins). The role involves supervising the purification process, managing manpower, ensuring equipment readiness, and maintaining quality and safety standards.
Role & responsibilities
Key Responsibilities:
1. Shift Operations Management
- Supervise all downstream production activities, including harvest, filtration, chromatography, ultrafiltration/diafiltration (UF/DF), and formulation.
- Ensure batch manufacturing records (BMRs) are followed strictly as per approved procedures and cGMP guidelines.
- Monitor process parameters (flow rates, pressures, conductivity, pH, temperature, etc.) and record data accurately.
- Perform in-process checks and ensure timely sampling and coordination with the QC team.
- Oversee batch changeovers and line clearances between operations.
2. Team Leadership & Training
- Lead, train, and supervise production executives, operators, and contract staff during the shift.
- Allocate manpower effectively to ensure smooth workflow and timely batch execution.
- Conduct on-the-job training for team members on GMP, safety, and equipment operation.
3. Equipment & Process Management
- Ensure readiness, cleaning, and sterilization of all DSP equipment (e.g., chromatography skids, TFF systems, centrifuges, filtration units, mixers).
- Oversee CIP (Clean-in-Place) and SIP (Sterilize-in-Place) activities.
- Coordinate with Engineering for equipment maintenance, calibration, and troubleshooting.
- Review equipment logs and ensure timely updates in line with GMP compliance.
4. Documentation & Compliance
- Review and verify batch records, logbooks, and cleaning records for accuracy and completeness.
- Ensure compliance with cGMP, GDP (Good Documentation Practices), EHS (Environment, Health & Safety), and company quality standards.
- Identify and report deviations, non-conformances, and assist in root cause analysis and CAPA implementation.
- Support internal and external audits and provide necessary process documentation.
5. Coordination & Communication
- Collaborate with Upstream (USP), QA, QC, Warehouse, and Engineering teams for coordinated production activities.
- Communicate critical process issues, equipment alarms, or safety incidents promptly to the Production Manager.
- Participate in daily production review meetings and contribute to process optimization initiatives.
Preferred candidate profile
Key Competencies:
- Leadership and team management.
- Strong analytical and troubleshooting abilities.
- Excellent communication and documentation skills.
- Focus on quality, safety, and regulatory compliance.
- Ability to work effectively in a 247 shift environment.
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