India's DMPLOI - Jobs & Networking AppKLM Laboratories Pvt. Ltd., a growing pharmaceutical organization committed to quality, innovation, and scientific excellence, is inviting applications for the Analytical Development Laboratory (ADL) department. This opportunity is ideal for professionals with analytical research and method development experience who are looking to advance their careers in pharmaceutical development and quality-focused environments.
The company is seeking talented candidates with expertise in analytical testing, method validation, laboratory instrument handling, and method transfer activities.
Position Details
Details
Company
KLM Laboratories Pvt. Ltd.
Department
Analytical Development Laboratory (ADL)
Qualification
B.Pharm / M.Sc. / B.Tech
Experience
2–4 Years
Location
Vadodara, Gujarat
Employment Type
Full-Time
Key Responsibilities
Selected candidates will be responsible for:
Analytical Method Validation for Finished Products (OSD, Topical & API)
Analysis using HPLC, UV Spectrophotometer, and Dissolution Instruments
Maintenance and Calibration of Laboratory Instruments
Method Transfer Activities to QC Laboratories
Documentation and compliance with pharmaceutical quality standards
Ensuring data integrity and regulatory compliance during analytical activities
Required Skills
Candidates should possess:
Hands-on experience with HPLC, UV, and Dissolution Systems
Knowledge of analytical method development and validation
Understanding of laboratory software and data management systems
Proficiency in MS Office applications
Good documentation and reporting skills
Strong analytical and problem-solving abilities
Why Join KLM Laboratories?
KLM Laboratories offers a professional work environment focused on innovation, quality, and continuous learning. Employees gain exposure to advanced analytical technologies, regulatory practices, and challenging pharmaceutical development projects that support career growth.
Application Process
Interested candidates can send their updated CV to:
Email: hr.unit3@klmlab.com
Subject Line: ADL – Analytical Development
Location Address:
Unit 3, City Survey No-12/2, Division-3 (Part B&C), Nareshwar Road, Manglej, Ta-Karjan, Dist.-Vadodara – 391243, Gujarat, India.
Technical FAQs
1. What is the purpose of analytical method validation in pharmaceutical laboratories?
Analytical method validation demonstrates that a testing method is suitable for its intended purpose by evaluating parameters such as accuracy, precision, specificity, linearity, robustness, and detection limits according to ICH guidelines.
2. Why is HPLC widely used in Analytical Development Laboratories?
HPLC provides high accuracy, sensitivity, and reproducibility for the identification and quantification of pharmaceutical compounds, impurities, degradation products, and assay determination.
3. What is method transfer in the pharmaceutical industry?
Method transfer is the documented process of transferring an analytical method from one laboratory (usually ADL) to another laboratory (typically QC) to ensure consistent performance and reliable results across sites.
4. What factors are checked during dissolution testing?
Dissolution testing evaluates drug release characteristics by monitoring parameters such as dissolution medium, temperature, agitation speed, sampling intervals, and percentage drug release over time.
5. Why is laboratory instrument calibration important?
Calibration ensures that analytical instruments produce accurate and reliable results. Regular calibration helps maintain regulatory compliance, data integrity, and consistent product quality.
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