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Job Responsibilities :

1.Lead the development and validation of analytical methods, including (but not limited to) impurity profiling methods for APIs, intermediates, starting materials, and drug products; author related study protocols and reports.

2.Resolve complex analytical challenges during project execution, e.g. : Method development for structural analogs?Analysis of highly polar compounds?Sample preparation in complex matrices

3.Address critical analytical issues requiring advanced technical expertise.

4.Demonstrate mastery of analytical instrumentation principles, operations, and hyphenated techniques (e.g., LC-MS, GC-MS) to solve analytical problems.

5.Perform routine instrument maintenance and calibration.

Qualifications :

1.Ph.D. in Pharmaceutical Sciences, Analytical Chemistry, Physical Chemistry, or related disciplines.

2.Proven experience in developing chromatographic methods for diverse systems (small molecules / peptides). Preferred candidates will have : Background in organic chemistry / drug degradation chemistry?Experience with chiral isomer separation or peptide racemization studies?Expertise in complex sample preparation / post-treatment

3.Strong GMP compliance mindset, excellent communication skills, resilience to demanding workloads, and proactive problem-solving attitude.