Executive Quality Control

Abbott Laboratories; Solan; On-site; INR 600,000 - 800,000; Full time

Job summary

Abbott Laboratories is seeking a Quality Control professional in India (Village Mauza: Baddi) with 2-4 years of experience in Chemical & Instrumental analysis for finished goods and stability. You will perform stability testing, calibrate core instruments, and ensure timely reporting within GLP/GMP frameworks.

The role requires B.Pharm or M.Sc., familiarity with LIMS, and strict adherence to quality standards.

Qualifications

• B.Pharm or M.Sc. with 2-4 years in QC.
• Experience in stability/finished product analysis.
• Familiarity with GLP/GMP requirements.

Responsibilities

• Analyze Stability Samples/Finished Products as per STP/Specifications in QC of Hormone block.
• Calibrate routine instruments (Balance, pH meter, Conductivity meter) as needed.
• Timely analysis of stability samples and reporting abnormalities.
• Sample charging, withdrawal, and documentation in Stability Chambers; data entry in LIMS.
• Report stability/finished product results and ensure compliance with specifications.
• Ensure adherence to GLP/GMP and data integrity.

Skills

Quality control

GLP/GMP compliance

Data analysis

Education

B.Pharm

M.Sc

Tools

LIMS

Balance

pH meter

Conductivity meter

Job description

Location India > Village Mauza : Baddi Category Quality

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 time
• 9. 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.

Followings will be the responsibilities of the position holder:1. Compliance of current Good Manufacturing Practices in the Oral dosage facility & to follow GDP with data-integrity complia

Job Id 31163674 LocationIndia > Village Mauza : Baddi Medical surveillance Not Applicable Division EPD Established Pharma Travel Not specified Additional Location Significant work activities Continuous standing for prolonged periods (more than 2 consecutive hours in an 8 hour day)

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