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Team Member Engineering – Instrumentation

6-12 Years
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Job Description

Job Purpose

To ensure the reliable operation, calibration, troubleshooting, and automation support for all equipment-related instrumentation across the pharma manufacturing site, enabling compliant, safe, and uninterrupted production in line with cGMP, data integrity, and regulatory requirements.

Roles & Responsibilities

1. Equipment Instrumentation Management

  • Manage field instruments used in manufacturing equipment, including:
    • RMG, FBD, Blenders, Tablet Press, Coaters
    • Encapsulation & Softgel equipment
    • Derma mixers, homogenizers, reactors
    • Packing line instruments (sensors, cameras, checkweighers)
  • Ensure continuous availability and performance of critical process instruments.
  • Monitor and maintain transmitters, indicators, load cells, gauges, sensors, and control elements.

2. Automation System Management

  • Support PLC / SCADA / HMI systems for process equipment.
  • Execute modifications to logic, alarms, and interlocks under proper change control.
  • Ensure automation systems comply with 21 CFR Part 11 and data integrity requirements.
  • Coordinate with automation vendors for advanced troubleshooting and upgrades.

3. Calibration & Compliance

  • Execute calibration of all equipment instruments as per schedule.
  • Maintain calibration labels, records, traceability certificates, and calibration history.
  • Investigate out-of-calibration (OOC) events and support impact assessment.
  • Ensure compliance with cGMP, ALCOA+, GLP, and site QC/QA expectations.

4. Breakdown, Preventive & Predictive Maintenance

  • Attend equipment-related instrumentation breakdowns to minimize downtime.
  • Perform preventive maintenance of instruments and automation panels.
  • Diagnose and resolve issues like signal failures, drift, noise, and PLC communication faults.
  • Support predictive maintenance activities using trend data and failure history.

5. Documentation & QMS Requirements

  • Maintain and update:
    • Calibration records
    • Instrument history cards
    • Maintenance and breakdown logs
    • Job completion reports
  • Ensure compliance with SOPs, deviations, CAPA, change control, and internal audit requirements.
  • Ensure all documentation is accurate, contemporaneous, and audit-ready.

6. Cross-Functional Coordination

  • Work with Production to ensure equipment readiness and process continuity.
  • Coordinate with QA for calibration approvals, deviations, and audit responses.
  • Support QC during instrument-related sampling/testing requirements.
  • Collaborate with Engineering / Maintenance teams for utilities/equipment support.

7. Safety, EHS & Good Engineering Practices

  • Follow electrical safety, LOTO, PPE, and MSDS guidelines.
  • Ensure safe working during instrumentation maintenance in GMP zones.
  • Maintain 5S and housekeeping in instrument rooms, panels, and shopfloor areas.

8. Audit & Inspection Support

  • Support internal audits, customer audits, and regulatory inspections.
  • Provide instrumentation/automation documents and explain system controls.
  • Ensure timely closure of audit observations related to instrumentation.

9. Continuous Improvement & Digitalization

  • Drive improvements to enhance instrument reliability, MTBF, and reduce failures.
  • Implement Lean, Kaizen, TPM initiatives for equipment instrumentation.
  • Support digital data collection, dashboards, and automation enhancements.

Educational Qualification

  • Diploma / B.E. / B.Tech in:
    • Instrumentation Engineering
    • Electronics & Instrumentation
    • Electronics Engineering
    • Electrical Engineering (with instrumentation exposure)
  • Certification in PLC / SCADA / Automation is an added advantage.

Experience

  • 6-12 years of experience in equipment instrumentation and automation in a pharma manufacturing site.
  • Hands-on work with field instruments, PLC/SCADA systems, and GMP documentation.
  • Experience in regulated environments (US-FDA, EU-GMP, WHO-GMP) preferred.

Key Skills & Competencies

  • Strong knowledge of equipment instrumentation
  • PLC/SCADA troubleshooting skills
  • Calibration, maintenance & validation exposure
  • Understanding of cGMP, data integrity & pharma processes
  • Good documentation discipline
  • Problem-solving & RCA (Root Cause Analysis) capability

More Info

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About Company

Job ID: 149278865