Executive Quality Control

Abbott; India; On-site; INR 350,000 - 550,000; Full time

Job summary

Abbott in India (Baddi) seeks a QC Analyst with 2–4 years in chemical and instrumental analysis for finished goods and stability. You will perform stability testing, calibrate instruments, ensure timely reporting, and maintain GLP/GMP compliant documentation.

Your role includes LIMS data entry, sample reconciliation, and adherence to SOPs. Travel is not specified; standard work shift applies.

Qualifications

• B.Pharm / M.Sc with 2-4 years in Chemical & Instrumental QC analysis.
• Experience in chemical and instrumental analysis for finished goods and stability.
• Familiarity with GLP/GMP requirements and quality documentation.

Responsibilities

• Analyze stability samples and finished products as per STP/specifications in Quality Control.
• Calibrate routine instruments like balance, pH meter and conductivity meter as needed.
• Ensure timely analysis of stability samples and reporting of abnormalities.
• Charge, withdraw and document stability samples within deadlines.
• Reconcile samples and maintain stability destruction records.
• Maintain GLP/GMP compliance and documentation.
• Operate and input data in LIMS and related software.
• Complete trainings on GLP/GMP on time.
• Report stability/finished product results and compare with specs.
• Evaluate results per SOP and inform supervisor of abnormalities.

Skills

QC Analysis

GLP/GMP

Instrument calibration

Education

B.Pharm or M.Sc

Tools

LIMS

Balance

pH meter

Conductivity meter

Job description

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.

The base pay for this position is N/A In 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)