jobiwork
Kia Biopharma Technologies logo
Kia Biopharma Technologies
From company careers site

Supervisor

Location
Indore
Work mode
On-site
Employment type
Full-time

About the job

Purpose: The Electrical/Mechanical/Instrumentation Engineer will be responsible for operation, maintenance, and compliance of Electrical/Mechanical/Instrumentation systems across OSD manufacturing and packaging areas. The role includes manufacturing equipment preventive/breakdown maintenance, calibration, shift operation responsibility, documentation of all GMP activity. Active participation in regulatory and Quality Management System (QMS) documentation in accordance with cGMP requirements.

Position / Job Title: Supervisor – Manufacturing Maintenance, Engineering

Department: Engineering/Technical services

Reporting To: Manager, Engineering

Location: Pithampur

Years of Experience: 05–08 years of experience in OSD Plant maintenance and troubleshooting

Dosage Form: Solid & Semi solid

Job Responsibilities / Deliverables: 1. Manufacturing Process Equipments Maintenance & Troubleshooting Perform operation, preventive, and breakdown maintenance of manufacturing process equipment, including: Granulation lines (RMG, FBD, Mill, Blender) Dispensing units and material handling systems Coating machines (Auto coaters) Compression machines Track & Trace systems Primary packaging areas (Blister, Strip, Bottle lines etc.) Secondary packaging areas (Cartoner, BPU, Case packer, Serialization equipment etc.) Ensure minimum downtime and high equipment availability through timely troubleshooting and root cause analysis. Maintain shift wise report and update MTBF and MTTR accordingly. Support continuous manufacturing operations with prompt response to breakdowns. Handle modifications, upgrades, and retrofits of manufacturing equipment as per approved change controls. Tracking of PM schedule and completing the PM activity within schedule online in E log software.

2. Calibration Management Ensure compliance with calibration schedules for instruments used in manufacturing, warehouse and quality Control. Review calibration results and support investigation of out-of-tolerance (OOT) conditions. Initiate and close calibration-related deviations, RCA, and CAPA in collaboration with QA.

3. EHS & Statutory Compliance Ensure adherence to safety norms, statutory guidelines, and site EHS policies. Implement and monitor LOTO practices, permit-to-work systems, and use of electrical PPE. Participate in electrical safety audits, EHS inspections, and incident investigations. Maintain compliance of earthing, lightning protection, and electrical safety testing. 4. Regulatory & QMS Documentation Actively participate in QMS activities related to engineering and manufacturing, including: Change Control (CC) Deviation and incident handling CAPA implementation and effectiveness review Prepare, review, and maintain SOPs, logbooks, and technical documentation for process equipment systems. Support regulatory audits and inspections (USFDA, WHO, MHRA, EU) by providing technical inputs and maintaining documentation.

5. Qualification & Validation Support Support IQ/OQ/PQ and requalification activities for manufacturing equipment, utilities, and control systems. Coordinate with QA and Validation teams to ensure compliance with validated state requirements.

6. Continuous Improvement Drive improvement initiatives related to equipment reliability, energy efficiency, and maintenance optimization. Analyse recurring failures and implement preventive measures. Support digitization and predictive maintenance initiatives.

Qualifications Education: Bachelor’s degree in Electrical/Mechanical/Instrumentation (mandatory).

Additional notes: Skills & Competencies Strong understanding of OSD manufacturing equipment systems cGMP and regulatory compliance knowledge Calibration and validation exposure Documentation and audit readiness mindset Effective coordination with Production, QA, Validation, and EHS teams Ability to read engineering drawings (P&ID, Electrical drawings, layout). Exposure to regulatory audits: USFDA, EU-GMP, WHO. Familiarity with QMS software / electronic PM software is an advantage.

Key Performance Indicators (KPIs) Zero Quality Incidents 100% adherence of PM Schedular 100% calibration schedular Zero Safety Incidents

From Kia Biopharma Technologies's careers page (Company careers page), checked 29 Oct 2026.

How to apply

  1. Select Apply on rubicon.co.in. It opens Kia Biopharma Technologies's own application form in a new tab, run on Company careers page.
  2. Fill in the form and upload your résumé there. Jobiwork never sees your application.
  3. Kia Biopharma Technologies will reply to you directly. No real employer asks you for money to apply.

Posted 27 Oct 2026 · checked 29 Oct 2026 · Report this job

Get new Other jobs in Indore by email

Free account: job alerts, every search result and full descriptions. No phone number, no résumé upload.

Create job alert

Similar jobs

Companies hiring in Indore

All jobs in Indore →