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Natco Pharma
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Walk-in Interview For Maintenance/Production/EHS/QA/QC & Micro

Walk-in Interview For Maintenance/Production/EHS/QA/QC & Micro

Natco Pharma

3 - 8 years

3 - 8 Lacs

chennai

Posted:1 week ago| Platform:

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Skills Required

qc production safety maintenance api chiller microbiology icp-ms instrumentation ahu boiler qa ehs aqa utilities reactors mlt electrical gc hazard identification hplc quality control documentation em compressors calibration gmp gc-ms bet oos oot qms 21 cfr bulk drugs work permit lcms

Work Mode

Work from Office

Job Type

Full Time

Job Description

NATCO Pharma is hiring!

Join us for a walk-in interview on 06th December 2025 in Chennai across key functions: Maintenance, Production, EHS, QA, QC & Microbiology.

Be part of a team that is committed to quality, innovation, and excellence in API manufacturing.

Job Requirements

Maintenance - Utilities / Mechanical / Electrical / Instrumentation

Qualification:

Operator: 3 to 5 yrs
(Utilities Water Systems, AHUs, Compressors, Chillers, Boilers)
Supervisor: 7 to 10 yrs
(Process & Utility Equipment Maintenance, GMP Documentation)
Instrumentation Operator: 2 to 3 yrs
(Calibration, Automation)
Electrical Operator: 3 to 5 yrs
(HT/LT Operation, Generator Maintenance, Electrical Projects)
Asst. Manager: 10 to 12 yrs
(Electrical & Instrumentation Maintenance, GMP Documentation & QMS)
Instrumentation Supervisor: 8 to 10 yrs
(PLC Automation, Validation, Calibration, 21CFR compliance Software & its Qualification)

Production (API) Operator / Supervisor / Assistant Manager

Qualification:

Operator: 1 to 5 yrs (
AGR & Reactor Operation, Clean Room Manufacturing)
Supervisor: 1 to 5 yrs
(GMP Compliance, Documentation)
Asst. Manager: 10 to 13 yrs
(Overseeing Manufacturing, Regulatory Standards, Process Improvements)

EHS (Safety)

Qualification:

Supervisor: 3 to 5 yrs
(Hazard Identification, Risk Assessment, Safety Training, issuing work permit systems, Emergency Drills)

QA Chemist / Officer

Qualification:

Possess 2 to 8 years of experience in handling IPQA and Analytical QA activities, including techniques such as ICP-MS, LC-MS, and GC-MS

Quality Control Analysts / Reviewer / Shift In-charge

Qualification:

Analyst: 4 to 7 yrs
(GC/HPLC, ICP-MS/GC-MS/LC-MS, Empower Software)
Reviewer:

8 to 10 yrs
(RM/INP/INT/FP/Stability Analysis, Deviation/OOS/OOT Investigations)
Asst. Manager: 10 to 12 yrs
(Analytical Method Validation, Method Transfer, ICP-MS/LC-MS/GC-MS)

QC (Microbiology)

Qualification:

Analyst: 8 to 10 yrs
(MLT & BET Method Validation, Environmental Monitoring, trend preparation, and Disinfectant efficacy validation)

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