Job Title: Quality Control Specialist – LIMS & Instrumentation
Job Summary
* Location: Chennai, Tamil Nadu
* Industry: Pharmaceutical
* Experience Required: 2 to 5 years in Pharmaceutical Quality Control
* Qualification: B.Sc/M.Sc in Chemistry or B.Pharm/M.Pharm
* Core Competencies: Expertise in HPLC, GC, and Laboratory Information Management Systems (LIMS)
Company Overview
We are a leading organization in the pharmaceutical sector committed to maintaining the highest standards of product quality and patient safety. Our laboratory operations are driven by precision, innovation, and strict adherence to global regulatory standards. We are currently seeking a dedicated and detail-oriented Quality Control Specialist to join our team in Chennai. This position is ideal for an experienced professional looking to integrate advanced analytical instrumentation with digital quality management systems.
Role Description
As a Quality Control Specialist focused on LIMS and instrumentation, you will play a critical role in ensuring that our pharmaceutical products meet rigorous safety and quality benchmarks. You will be responsible for the seamless operation of analytical equipment and the accurate management of data within our laboratory systems. Your day-to-day responsibilities will involve a blend of hands-on technical testing and systematic data management.
Key Responsibilities
Analytical Testing and Instrumentation:
You will perform routine and advanced quality control testing. This includes the operation, calibration, and troubleshooting of sophisticated laboratory instruments, specifically Gas Chromatography (GC) and High-Performance Liquid Chromatography (HPLC). Ensuring that all systems are suitable for their intended use and compliant with testing protocols is a fundamental part of this role.
LIMS Management:
You will be responsible for the end-to-end management of sample tracking using the Laboratory Information Management System (LIMS). This includes logging samples upon arrival, tracking their progress through the testing lifecycle, and ensuring that all data is entered with precision. You will be tasked with reviewing and verifying analytical data to ensure complete accuracy before final reports are generated.
Compliance and Documentation:
Maintaining the highest standards of Good Manufacturing Practices (GMP) and Good Laboratory Practices (GLP) is mandatory. You will be responsible for drafting accurate technical reports, including Certificates of Analysis (CoA). Furthermore, you will play an active role in maintaining data integrity across all electronic and paper-based records.
Quality Investigations:
When results fall outside of established specifications, you will be required to participate in investigations. This includes documenting and analyzing Out of Specification (OOS) and Out of Trend (OOT) results, performing root cause analysis, and ensuring that all deviations are handled in accordance with company standard operating procedures and regulatory guidelines.
Qualifications and Experience
To be considered for this role, candidates must meet the following criteria:
* Academic Background: A degree in B.Sc or M.Sc in Chemistry, or B.Pharm/M.Pharm from a recognized institution.
* Professional Experience: 2 to 5 years of proven experience within a pharmaceutical Quality Control department.
* Technical Proficiency: Hands-on experience with chromatography techniques, specifically HPLC and GC, is essential.
* System Knowledge: Demonstrated proficiency in using Laboratory Information Management Systems (LIMS).
* Regulatory Understanding: A comprehensive understanding of GMP/GLP guidelines and a strong commitment to data integrity.
* Soft Skills: Strong analytical thinking, excellent attention to detail, and the ability to maintain accurate documentation under strict timelines.
Why Join Us?
Joining our team offers the opportunity to work in a sophisticated laboratory environment that values technical excellence and professional growth. You will be an integral part of a process that ensures the reliability of life-saving pharmaceutical products. We provide a structured work environment where you can refine your skills in both instrumentation and digital quality informatics.
How to Apply
If you are a motivated professional with the required expertise and a passion for pharmaceutical quality control, we encourage you to apply. Please submit your updated resume to [email protected].
Please ensure that your email includes the following subject line: Application for QC – LIMS & Instrumentation.
We are looking for candidates who are eager to contribute to a high-performance team. Only shortlisted candidates will be contacted for the next steps in the recruitment process. We look forward to reviewing your application.