Executive Quality Control

Thornton Tomasetti; Solan; On-site; INR 450,000 - 750,000; Full time

Job summary

Thornton Tomasetti is seeking an Executive Quality Control professional in India (Baddi region) with 2–4 years of experience in chemical and instrumental QC analysis. The role involves stability testing of finished products, instrument calibration, and strict GLP/GMP adherence in a pharmaceutical QC environment.

The incumbent will handle stability sample management, data entry in LIMS, and timely reporting of results to supervisors, ensuring compliance with SOPs and quality standards.

Qualifications

• B.Pharm or M.Sc. with 2–4 years in chemical and instrumental QC analysis.
• Experience in stability studies, finished products, and GLP/GMP.
• Familiar with instrument calibration and documentation in QC labs.

Responsibilities

• Analyze stability samples and finished products as per SOPs.
• Calibrate routine instruments (balance, pH meter, conductivity meter).
• Ensure timely analysis and reporting of stability data.
• Manage stability sample charging, withdrawal, and reconciliation.
• Maintain GLP/GMP compliance in daily activities and records.

Skills

Quality control

Stability testing

Instrumental analysis

GLP/GMP compliance

Calibration

Education

B.Pharm

M.Sc.

Tools

LIMS

HPLC

Balance

pH meter

Conductivity meter

Job description

## Executive Quality ControlApply: India > Village Mauza : Baddi: Full time: Posted Today: End Date: October 9, 2026 (3 days left to apply): 31163674## **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:1. Analysis of Stability Samples/ Finished Products as per respective STP/Specification in Quality Control of Hormone block.2. Calibration of routine usage instruments such as Balance, pH meter and Conductivity meter, as and when required.3. Timely analysis of stability sample and report if any abnormality observed.4. Timely Charging & withdrawal of samples from Stability Chambers & their documentation within the time frame.5. Sample reconciliation and destruction record of stability sample.6. Implementation of GLP / GMP requirements.7. Stability sample charging, Withdrawal, Reconciliation and data entry in software such as LIMS.8. Completion of assigned trainings of GLP/GMP on time9. Reporting of stability/Finished product sample as per report received from outside Laboratory and check the compliance against respective specifications.10. Evalutates the analysis results as per SOP and report to the supervisor for any abnormality.**The base pay for this position is**N/AIn specific locations, the pay range may vary from the range posted.## **JOB FAMILY:**Operations Quality## **DIVISION:**EPD Established Pharma## **LOCATION:**India > Village Mauza : Baddi## **ADDITIONAL LOCATIONS:**## **WORK SHIFT:**Standard## **TRAVEL:**Not specified## **MEDICAL SURVEILLANCE:**Not Applicable## **SIGNIFICANT WORK ACTIVITIES:**Continuous standing for prolonged periods (more than 2 consecutive hours in an 8 hour day)