Job description
Join NexaChem Solutions, a leading innovator in analytical chemistry and pharmaceutical sciences, to accelerate discovery and ensure product quality across markets.
We are seeking a Senior Analytical Chemist who thrives in a fast-paced, collaborative environment. You will design and validate robust analytical methods, supervise method transfers, and mentor junior scientists while upholding GLP/GMP standards.
What you’ll do is anchored in method development, validation, and cross-functional collaboration to support regulatory submissions and product quality. You’ll work with state-of-the-art instrumentation and contribute to a culture of scientific excellence.
Responsibility
- Lead development and validation of analytical methods (HPLC, LC-MS, GC, UV-Vis) for APIs, impurities, and stability samples.
- Oversee method transfer to quality control and manufacturing, ensuring robust documentation and compliance with GMP/GLP.
- Design experiments to support regulatory submissions (ICH guidelines); prepare technical reports and method documentation.
- Analyze data, troubleshoot instrumentation, and optimize platform performance to improve throughput and data integrity.
- Collaborate with R&D, QC, and manufacturing teams; present findings to stakeholders and senior management.
- Mentor and train junior scientists; supervise analysts on projects and development plans.
- Maintain instrument calibration, preventive maintenance, and inventory management for analytical equipment.
Qualification
- Master’s degree in Analytical Chemistry, Chemistry, or a closely related field; PhD is a plus.
- 5+ years of hands-on experience in pharmaceutical/chemical analytics, with strong method development and validation background.
- Proficiency with HPLC/UHPLC, GC, LC-MS/MS, and related data analysis software (Empower, ChemStation, MassHunter, etc.).
- Experience with regulatory guidelines (FDA, ICH Q2/Q3/Q7) and method transfer/validation processes.
- Strong problem-solving, data integrity, and technical writing skills; excellent communication and teamwork abilities.
- Experience in cross-functional collaboration and technical reporting for regulatory submissions.
- Knowledge of QA/QC processes and instrument maintenance; ability to manage multiple projects simultaneously.