ROLE SUMMARY
To manage production activities and manpower during the assigned shift, ensure manufacturing processes and quality records are completed as per SOPs, and maintain cGMP, safety and equipment readiness requirements.
KEY RESPONSIBILITIES
To manage the manpower in shift.
To perform manufacturing process and fill the quality records (i.e., BMR/BPR/ECR/Logbooks) as per SOPs.
To maintain cGMP and safety norms. To distribute manpower as per requirement of manufacturing process with optimum utilization of plant capacity.
To ensure batch charging, sampling procedure, equipment cleaning is done as per SOP/BMR/ECRs
To monitor and record humidity and temperature
To verify the activity of calibration/qualification of equipment & instruments. To co-ordinate with maintenance department to reduce unplanned breakdown/preventive maintenance.
To schedule required training of the personnel working in the plant
To be well versed with GMP & ICHQ7.
To co-ordinate with Engineer/QC/QA.
QUALIFICATIONS & EXPERIENCE
B.Sc. / HND in Chemical Engineering.
At least 5 years of production operations experience in chemical synthesis or the pharmaceutical API industry, including shift coordination.
MANAGERIAL COMPETENCIES
Shift manpower management
Planning and coordination
Training and communication
Teamwork and accountability
TECHNICAL COMPETENCIES
Manufacturing process execution
BMR/BPR/ECR and logbook documentation
GMP and ICH Q7 requirements
Batch charging, sampling and equipment cleaning
Calibration and qualification verification
WHAT WE OFFER
Competitive salary and performance-based bonuses.
A supportive and dynamic work environment with clear career growth opportunities.
Comprehensive medical insurance, pension, and other employee benefits.