Hiring For Liquid Operator / Technician | Project Plant | Roorkee

Walter Bushnell; Haridwar; On-site; INR 240,000 - 300,000; Full time

Job summary

Walter Bushnell is seeking a Liquid Operator to set up, operate, and clean pharmaceutical liquid machinery in a regulated facility. You will ensure compliance with SOPs, cGMP guidelines, and daily production targets while maintaining batch records and logbooks.

The role requires hands-on operation experience in a USFDA or regulated environment, with focus on quality checks, changeovers, and strict hygiene protocols to safeguard product integrity.

Qualifications

• 2 to 5 years of hands-on machine operation in a USFDA or regulated oral liquid pharmaceutical facility.

Responsibilities

• Operate liquid mixing vessels, homogenizers, transfer pumps, bottle washing, monoblock filling, ROPP capping, induction sealing, and labeling machines.
• Perform routine quality checks (fill volume variation, sealing integrity, cap torque, leak tests) and secure Line Clearance.
• Execute Clean-in-Place (CIP) cycles, sanitization, and handle machine change parts during batch changeovers.
• Maintain real-time, accurate online entries in Batch Manufacturing Records (BMR), Batch Packing Records (BPR), and equipment logbooks.
• Adhere strictly to personal hygiene, cleanroom gowning, and plant safety (EHS) protocols.

Skills

Troubleshooting

Change-part handling

GDP (Good Documentation Practices)

Education

ITI (Fitter/Electrical/Mechanical)

Diploma (Pharmacy/Engineering)

12th Standard

Job description

The Liquid Operator is responsible for setting up, operating, and cleaning pharmaceutical liquid manufacturing and filling machinery. This role ensures strict compliance with SOPs, cGMP guidelines, and daily production targets.

Key Responsibilities

• Machine Operation: Operate liquid mixing vessels, homogenizers, transfer pumps, bottle washing, monoblock filling, ROPP capping, induction sealing, and labeling machines.
• In-Process Quality (IPQC): Perform routine quality checks (fill volume variation, sealing integrity, cap torque, leak tests) and secure Line Clearance.
• Cleaning & Changeover: Execute Clean-in-Place (CIP) cycles, sanitization, and handle machine change parts during batch changeovers.
• cGMP Documentation: Maintain real-time, accurate online entries in Batch Manufacturing Records (BMR), Batch Packing Records (BPR), and equipment logbooks.
• Safety & Compliance: Adhere strictly to personal hygiene, cleanroom gowning, and plant safety (EHS) protocols.

Qualifications & Experience

• Education: ITI (Fitter/Electrical/Mechanical), Diploma (Pharmacy/Engineering), or 12th Standard.
• Experience: 2 to 5 years of hands-on machine operation in a USFDA or regulated oral liquid pharmaceutical facility.
• Skills: Hands-on machine troubleshooting, change-part handling, and strong Good Documentation Practices (GDP).