Executive Quality Control Position at Abbott Laboratories in Baddi
An Abbott Quality Control opportunity has emerged for qualified candidates to join Abbott Laboratories as an Executive in Quality Control at their Baddi facility. This full-time role calls for individuals with a B.Pharm or M.Sc. degree and 2–4 years of relevant experience in chemical and instrumental analysis.
About the Company
Abbott Laboratories is a global healthcare company that develops and manufactures a wide range of medical devices, diagnostics, nutritional products, and branded generic pharmaceuticals. With a commitment to improving lives through innovative solutions, Abbott operates in various sectors, including pharmaceuticals and diagnostics, and is headquartered in Abbott Park, Illinois, USA.
Job Details
- Company: Abbott Laboratories
- Location: Baddi, Himachal Pradesh, India
- Employment Type: Full-time
- Job ID: 31159922
- Experience Required: B.Pharm / M.Sc. with 2–4 years of experience in Chemical & Instrumental analysis QC (Finished goods & stability). Approved Chemist-licensed candidates shall be preferred. Candidates should be well-versed in CAPA and GMP documentation, with exposure to regulatory audits such as MHRA and USFDA.
Abbott Quality Control Job Description
The Executive in Quality Control will be responsible for the analysis of stability samples and finished products according to the respective Standard Testing Procedures (STP) and specifications. This Abbott Quality Control role includes calibration of routine usage instruments, timely analysis and reporting of stability samples, and ensuring compliance with GLP and GMP requirements.
Key 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 samples and report any abnormalities observed.
- Timely charging & withdrawal of samples from Stability Chambers & their documentation within the time frame.
- Sample reconciliation and destruction record of stability samples.
- 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 trainings of GLP/GMP on time.
- Reporting of stability/Finished product sample as per report received from outside Laboratory and checking compliance against respective specifications.
- Evaluates the analysis results as per SOP and reports to the supervisor for any abnormalities.
How to Apply
Interested candidates should apply through the official Abbott careers page:
Conclusion
This is an excellent opportunity for qualified professionals to advance their careers in this Abbott Quality Control role. Candidates are encouraged to apply before the deadline to secure their chance at this pivotal role in Quality Control.
