Shift Incharge

We are Sisco Jobs a recruitment consultancy based in Trichy Tamil Nadu. We are hiring for the position of Shift Incharge in Chennai Tamil Nadu. The role is focused on pharmaceutical/API production operations and requires an experienced professional capable of supervising manufacturing activities maintaining regulatory compliance monitoring critical process parameters and coordinating with cross-functional teams. If you meet the requirements below apply early as positions are limited.

• Supervise all production activities during the assigned shift and ensure achievement of scheduled production targets.
  
• Monitor API manufacturing operations including reaction distillation filtration centrifugation drying milling and blending.
  
• Ensure strict compliance with cGMP GDP EHS SOPs and applicable quality requirements.
  
• Verify line clearance equipment readiness raw-material availability utilities and manufacturing documentation before batch initiation.
  
• Review and maintain Batch Manufacturing Records equipment usage records logbooks and shift reports.
  
• Monitor critical process parameters and ensure manufacturing operations remain within validated process limits.
  
• Coordinate with QA QC Warehouse Engineering Utilities and EHS teams to maintain uninterrupted production.
  
• Investigate deviations equipment breakdowns and production issues and participate in RCA and CAPA implementation.
  

1. API Manufacturing: Hands-on understanding of pharmaceutical/API production processes including reaction filtration centrifugation drying milling and blending.
   
2. cGMP & GDP Compliance: Ability to execute and supervise manufacturing activities according to regulated pharmaceutical practices.
   
3. Production Documentation: Experience reviewing BMRs logbooks equipment records and shift documentation.
   
4. Process Monitoring: Ability to monitor critical process parameters and maintain operations within validated limits.
   
5. Deviation / RCA / CAPA: Practical knowledge of investigating production deviations and supporting corrective and preventive actions.
   

• Process and cleaning validation exposure.
  
• Technology transfer experience.
  
• Strong understanding of equipment cleaning sanitization and product changeover procedures.
  

Candidates should have 4 years of experience preferably in pharmaceutical/API manufacturing or a closely related production environment. Experience should include shift production supervision regulated manufacturing documentation process monitoring equipment operations and coordination with Quality Engineering Warehouse and EHS functions.

• Minimum: Typical / / B.E / Diploma in Chemical Engineering Chemistry Pharmaceutical Technology or a related discipline
  
• Preferred: Typical Degree in Chemical Engineering / Pharmaceutical Technology
  
• Additional: Training or certification in cGMP EHS process safety or pharmaceutical manufacturing is advantageous