2-5

Executive

5/10/2026

Perform HPLC and GC analysis following approved methods and standard operating procedures. Manage laboratory incidents, including OOS/OOT results, deviations, and QMS activities like CAPA and change control.

Working Hours

40 hours/week

Company Size

1 employee

Language

English

Visa Sponsorship

About The Company

Company was established in 1986 IOLCP is Indias one of the leading generic pharmaceutical company and is significant player in the Organic chemicals space. IOLCP has wide presence across various therapeutic categories like Pain Management Anti-diabetic Anti hypertensive Anti Convulsants etc. Our capabilities are nurtured by pursuing implementing the high standards of excellence in our operations. By delivering consistent results quality we have earned the admiration of customers and stakeholders. Innovative Strengths Strong Growth have made us the market leaders. We have built up our expertise responding to diverse customer requirements Our products cater to the key industrial sectors of Pharmaceutical Flexible Packaging Paint Lamination Ink Pesticides etc. Efficient teamwork strong associations have guided us to success. Accolades for our environmental policies have come from the highest levels of power. Through an unwavering focus on Quality Commitment Delivery we have charted our way to success in our operations and have won the admiration of our customers. Our success is built on the strong pillars of innovation quality dedicated customer service. By incorporating these other business strengths we have boosted our capabilities to maintain the leading edge in the industry earn the loyalty of our customers.

About the Role

Perform HPLC and GC analysis as per approved analytical methods and standard operating procedures (SOPs).
Conduct investigation of laboratory incidents, including deviations and non-conformances.
Handle and investigate OOS (Out of Specification) and OOT (Out of Trend) results in accordance with quality procedures.
Participate in QMS activities, including documentation, deviation management, CAPA, and change control where applicable.
Work in compliance with GLP (Good Laboratory Practices) and ensure proper documentation and data integrity.
Maintain laboratory records, logbooks, and analytical reports accurately.
Ensure proper handling, calibration, and maintenance of analytical instruments.
Support internal and external audits by providing required documentation and technical explanations.

Key Skills

HPLCGC AnalysisSOP ComplianceInvestigation of DeviationsOOS HandlingOOT HandlingQMSCAPAChange ControlGLPData IntegrityInstrument CalibrationAudit SupportAnalytical ReportingLaboratory Documentation