Company Description Aarti Pharmalabs Ltd. (APL) is a global provider of small-molecule drug substance CDMO services, partnering with leading pharmaceutical and biotech companies from first-in-human trials through commercial supply. The company delivers end-to-end development and manufacturing of RSMs, intermediates, and GMP APIs, with a strong focus on quality, speed, and regulatory compliance. APL’s diversified portfolio spans generic APIs, xanthine derivatives, HPAPIs, corticosteroids, cytotoxic and oncology products, supporting complex and high-value programs worldwide.

Its state-of-the-art R&D; and internationally accredited manufacturing facilities are inspected by agencies such as USFDA, EU-GMP, EDQM, KFDA, COFEPRIS, and ANVISA, ensuring robust compliance and reliable global supply. In addition to pharmaceuticals, APL is a preferred partner in Beverages and Nutraceuticals for Synthetic Caffeine, driven by innovation, science, and sustainability.

Role Description The Quality Control High Performance Liquid Chromatography (HPLC) Analyst is a full-time, in office role based in Tarapur. The role involves performing routine and non-routine HPLC analysis of raw materials, intermediates, in-process samples, and finished APIs in accordance with approved specifications, methods, and GMP requirements. The analyst will prepare standards and samples, calibrate and maintain HPLC systems, document results accurately,



and review chromatograms to ensure data integrity and compliance.

Daily responsibilities include supporting method validation and transfer, investigating out-of-specification and atypical results, and collaborating with Quality Assurance and Production teams to resolve quality-related issues. The analyst will also participate in laboratory audits, maintain proper records and logbooks, adhere to safety and regulatory guidelines, and contribute to continuous improvement of QC processes.

Qualifications

- Strong foundation in Quality Control principles, including analytical testing, documentation, and data integrity.
- Knowledge of Quality Assurance practices and Quality Management systems to support compliance and continuous improvement.
- Hands-on experience with Good Manufacturing Practice (GMP) in a pharmaceutical or chemical manufacturing environment.
- Exposure to Quality Auditing activities, such as internal audits, laboratory inspections, and audit readiness.
- Proficiency in HPLC operation, troubleshooting, and basic instrument maintenance; familiarity with chromatographic software.
- Bachelor’s or Master’s degree in Chemistry, Pharmaceutical Sciences, or a related discipline.
- Ability to interpret analytical data, write clear reports, and follow standard operating procedures with attention to detail.
- Effective collaboration skills and the ability to work in cross-functional teams within a regulated environment.

📌 Quality Control High Performance Liquid Chromatography Analyst (Tarapur)
🏢 Aarti Pharmalabs Ltd. (APL)
📍 Tarapur