Executive Quality Control

Abbott; Solan; On-site; INR 400,000 - 600,000; Full time

Job summary

Abbott in Solan (Himachal Pradesh) seeks a B.Pharm/M.Sc. holder with 2–4 years in chemical and instrumental QC analysis to handle stability samples and finished goods testing.

The role includes instrument calibration, GLP/GMP adherence, and data entry in LIMS, with rigorous documentation and timely reporting. The incumbent will ensure compliance with SOPs, coordinate sample charging/withdrawal, and complete mandatory GLP/GMP trainings, contributing to quality assurance across finished products

Qualifications

• B.Pharm or M.Sc. with 2–4 years in chemical and instrumental QC analysis.
• Experience with stability samples and finished goods testing.
• Knowledge of GLP/GMP requirements.

Responsibilities

• Analyze stability samples and finished products per STP/spec.
• Calibrate routine analytical instruments.
• Ensure timely analysis and reporting of abnormalities.
• Handle stability chamber sampling, documentation.
• Record sample reconciliation and destruction.
• Maintain GLP/GMP compliance.
• Enter data in LIMS and review results with supervisor.
• Complete GLP/GMP trainings on schedule.
• Report findings to supervisor and ensure compliance.

Skills

Chemical analysis

Instrumental analysis

Education

B.Pharm

M.Sc.

Tools

LIMS

Balance

pH meter

Conductivity meter

Job description

Experience Required : B.Pharm / M. Sc. with 2-4 years of experience in Chemical & Instrumental analysis QC (Finished goods & stability).

Followings will be the responsibilities of the position holder :

• Analysis of Stability Samples/ Finished Products as per respective STP/Specification in Quality Control of Hormone block.
• Calibration of routine usage instruments such as Balance, pH meter and Conductivity meter, as and when required.
• Timely analysis of stability sample and report if any abnormality observed.
• Timely Charging & withdrawal of samples from Stability Chambers & their documentation within the time frame.
• Sample reconciliation and destruction record of stability sample.
• Implementation of GLP / GMP requirements.
• Stability sample charging, Withdrawal, Reconciliation and data entry in software such as LIMS.
• Completion of assigned trainings of GLP/GMP on time
• Reporting of stability/Finished product sample as per report received from outside Laboratory and check the compliance against respective specifications.
• Evalutates the analysis results as per SOP and report to the supervisor for any abnormality.