Team Member - Manufacturing (Liquid) - Operator

SmartRecruiters, Inc.

Solan

On-site

INR 450,000 - 750,000

Full time

3 days ago
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Job summary

SmartRecruiters, Inc. is seeking a manufacturing operations professional for Oral Liquid Manufacturing. You will operate, calibrate, and validate instruments, and manage machine setup, operation and cleaning in the Oral Liquid area.

You will document process checks, support EBRs, e-logbooks, and calibration records, and drive lean improvements with 5S, Kaizen and safety initiatives in a compliant facility.

Qualifications

  • Diploma or graduation in pharmacy or engineering disciplines is mandatory.
  • 3–6 years of experience in manufacturing/production environments.
  • Experience with GMP/cGMP and regulatory standards is preferred.

Responsibilities

  • Operate, verify, calibrate, and properly use instruments in the Oral Liquid Manufacturing area.
  • Set up, operate, and clean manufacturing equipment in the Oral Liquid area.
  • Document in-process checks per approved BMRs and SOPs.
  • Troubleshoot to minimize downtime and operational risks during breakdowns.
  • Execute, review, and record Electronic Batch Records (EBRs) and related documents.
  • Perform CLITA activities and logging of safety/quality records in AMPLE system.

Skills

5S maintaining
MES operation
Lean Methodologies
Collaborative Problem Solving
Safety Awareness
Documentation
Audit Management
Compliance Management

Education

Diploma/Graduation in pharmacy, Mechanical, Electrical, Instrumentation Engineering or related field

Tools

PAS-X
ECR'S execution
SCADA/L2 batch reports

Job description

  • Full-time
  • Job Family: Manufacturing
  • Sub Job Family: Production - OSD
  • Preferred type of working: On-Premise
  • Business unit: GMO
Job Description

Role and responsibilities:

  • You will be responsible for the operation, verification, calibration, and proper use of instruments in the Oral Liquid Manufacturing area.
  • You will be responsible for machine setup, operation, and cleaning of all manufacturing equipment used in the Oral Liquid Manufacturing area.
  • You will be responsible for performing and documenting in-process checks in accordance with approved BMRs and SOPs.
  • You will be responsible for participating in troubleshooting activities to minimize operational risks and equipment downtime during breakdowns.
  • You will be responsible for the operation, verification, calibration, and proper utilization of manufacturing equipment in the Oral Liquid Manufacturing area.
  • You will be responsible for the execution, review, and recording of Electronic Batch Records (EBRs), e-logbooks, calibration and verification records, ECRs, and other related documents through PAS‑X (Process Automation System).
  • You will be responsible for the execution of CLITA activities and the logging, monitoring, and closure of Red Tags and White Tags in the AMPLE system.
  • You will be responsible for reporting and recording Near Misses, Unsafe Acts, and Unsafe Conditions in the SHEHUB system.
  • You will be responsible for reviewing and verifying SCADA/L2 batch reports to ensure accuracy, completeness, and compliance.
  • You will be responsible for documentation activity like deviations, calibration, change control etc. related to manufacturing area
  • You will be responsible for identifying process abnormalities, implementing lean tools such as 5S, Kaizen, and Autonomous Maintenance, and coordinating small project modifications with plant leads.

Skills & Attributes Functional Skills:

  • Computer System operation
  • Machine operation
  • 5S maintaining
  • MES operation
  • ECR'S execution
  • Technical Documentation
  • Audit Management
  • Compliance Management
  • Lean Methodologies
  • Workplace Safety
  • Behavioral Skills
  • Proactive Safety Awareness– Demonstrates vigilance in identifying hazards and enforcing safety protocols during maintenance activities.
  • Process Discipline and Documentation– Maintains accurate records, follows SOPs, and ensures compliance with GMP/cGMP and statutory standards.
  • Collaborative Problem Solving– Works effectively with cross-functional teams to troubleshoot issues, implement solutions, and drive continuous improvement.
  • Critical Exposures:
  • Experience in performing calibration of calibration, verification of manufacturing equipment's.
Qualifications

Educational Qualification

Diploma/Graduation in pharmacy, Mechanical, Electrical, Instrumentation Engineering or related field is mandatory.

Work Experience:

3 to 6 years of experience.

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