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Amneal Pharmaceuticals

Assistant, Manufacturing Injectables

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  • Posted 7 hours ago
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Job Description

Job Description B) SAT / IQ / OQ / PQ C) Routine Production D) GMP, EHS & Compliance F) Documentation

  • Design Review & FAT
  • Understand basket/loading layouts, spray arm motion, and filter housings.
  • Observe FAT demos of wash steps, detergents dosing, and HMI sequences.
  • Review utilities (DI/WFI, compressed air) and basic interlocks.
  • Verify nozzle layout, pump curves, filtration stages, and utilities.
  • Review interlocks/alarms; confirm safety and emergency stop logic.
  • Assess drainage paths and potential dead legs.
  • Support IQ/OQ: execute repeated wash cycles, sampling, and visual checks.
  • Document cycle parameters and assist in reproducibility verification.
  • Support PQ by preparing standardized loads and recording results.
  • Lead OQ: pressure/flow checks, sensor calibration, and cycle tuning.
  • Troubleshoot blocked nozzles, cavitation, and chemical dosing variability.
  • Support PQ reproducibility and finalize validated parameters.
  • Load parts as per pattern; verify chemical dosing and spray arm rotation.
  • Operate cycles; monitor pressures/temperatures; handle alarms.
  • Clean machine surfaces and maintain GDP-compliant records.
  • Perform PM on pumps, seals, filters; manage spares and change parts.
  • Trend wash performance; reduce rewash rates and downtime.
  • Coordinate with QA/Validation for periodic verification.
  • Adhere to cGMP, GDP, and site SOPs; ensure data integrity at all times.
  • Follow aseptic gowning and cleanroom behaviors for Grade A/B/C as applicable.
  • Comply with EHS guidelines; report near-misses/unsafe conditions promptly.
  • Maintain housekeeping (5S) and status labeling of equipment and areas.
  • Complete BMR/BPR entries, equipment logbooks, cleaning and line clearance records.
  • Support deviation/CAPA, change control, and risk assessments as applicable.
  • Maintain qualification/validation records during SAT, IQ, OQ, PQ.
  • Skills & Competencies
  • Technical: Understanding of equipment design, utilities, interlocks, and control logic.
  • Operational: Setup, start-up/shutdown, parameter verification, basic troubleshooting.
  • Behavioral: Attention to detail, teamwork, communication, ownership mindset.
  • Education & Experience
  • ITI/Diploma (Mech/Elect/Instr) / B.sc or B.Tech preferred.
  • 3 to 7 years of experience in sterile injectable manufacturing with hands-on equipment operation, FAT/SAT participation, troubleshooting, and qualification exposure (IQ/OQ/PQ).
  • Physical & Environmental Requirements
  • Ability to work in classified cleanrooms; prolonged standing; occasional lifting up to 20–25 kg.
  • Willingness to work in rotational shifts and extended hours during validation.

Qualifications

  • ITI/Diploma (Mech/Elect/Instr) / B.sc or B.Tech preferred.
  • 3 to 7 years of experience in sterile injectable manufacturing with hands-on equipment operation, FAT/SAT participation, troubleshooting, and qualification exposure (IQ/OQ/PQ).

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Job ID: 145655811

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