Abbott Hiring for Quality Control Jobs | M.Sc Chemistry Jobs
Searching for career-focused Quality Control Jobs in the pharmaceutical sector? Abbott Careers is hiring Executive Quality Control professionals for its manufacturing operations in Baddi. These M.Sc Chemistry Jobs provide opportunities to work in finished product analysis, stability testing, GMP documentation, and regulatory compliance activities. Candidates with pharmaceutical quality control experience and exposure to regulatory audits should explore this opportunity.
- Job Title: Executive Quality Control
- Location: Baddi
- Job Id: 31149445
About the Company:
Abbott Careers is part of Abbott, a globally recognized healthcare and pharmaceutical company operating across diagnostics, nutrition, medical devices, and medicines. The organization is known for maintaining high standards in manufacturing, quality assurance, and innovation. Through its pharmaceutical operations, Abbott offers professional growth opportunities in quality systems, analytical testing, and regulatory compliance.
Job Overview:
Abbott is recruiting for Quality Control Jobs for the role of Executive Quality Control at its Baddi facility. The role involves analysis of finished products and stability samples in the hormone block quality control department. Selected candidates will perform chemical and instrumental analysis, maintain GMP documentation, support GLP/GMP compliance, and manage stability sample handling activities. Candidates should also have exposure to regulatory audits such
as MHRA and USFDA.Responsibilities:
- 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 (Hormone block) 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.
- Coordinating and aligning the practices and procedures in line with the COBC requirements.
- Stability sample charging, Withdrawal, Reconciliation, and data entry in software such as LIMS.
- Completion of assigned training 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.
- Evaluates the analysis results as per SOP and report to the supervisor for any abnormality.
Educational Requirements:
- M. Sc. with 2-4 years of experience in Chemical & Instrumental analysis QC (Finished goods & stability). Approved chemist licensed candidate shall be preferred. Well versed with CAPA, GMP Documentation, should have exposure to regulatory audits such as MHRA, USFDA etc.
These Quality Control Jobs through Abbott Careers provide excellent opportunities for professionals seeking M.Sc Chemistry Jobs in pharmaceutical manufacturing and quality operations. With exposure to stability analysis, regulatory compliance, and GMP systems, this role offers valuable industry experience and long-term career growth. Candidates with pharmaceutical QC expertise should consider applying for this opportunity.
