We Are Hiring Associate Scientist!

Responsibilities

• Carry out routine tests on finished products, stability samples, raw materials, and CV samples using techniques such as assays, chromatographic purity, and particle size distribution.
• Evaluate test results and determine the acceptability of samples based on the results.
• Maintain accurate lab notebooks and complete all related analytical reports and documentation in compliance with Standard Operating Procedures (SOPs).
• Ensure laboratories are maintained with good housekeeping practices and in compliance with cGMP standards.
• Review lab notebooks promptly and ensure compliance with SOPs.
• Analyze and interpret results in both written and oral formats.
• Assist in training new analysts.
• Conduct laboratory investigations and initiate Quality Events, CAPA, and Change Controls as needed.
• Follow all SOPs and safety guidelines to ensure compliance with a cGMP environment.

Requirements

• Minimum 2 years of Experience in HPLC and Working in GMP Environment.
• Bachelor’s degree in Chemistry or related scientific field with 1-2 years of related experience in pharmaceutical analysis, or a Master’s degree with 1 year of experience.
• Problem-solving skills involving several concrete variables in standardized situations.
• Ability to perform necessary computations and interpret graphs.
• Working knowledge of instrumentation software used in laboratories.

Skills

• Minimum 2 years of Experience in HPLC and Working in GMP Environment.
• Bachelor’s degree in Chemistry or related scientific field with 1-2 years of related experience in pharmaceutical analysis, or a Master’s degree with 1 year of experience.
• Problem-solving skills involving several concrete variables in standardized situations.
• Ability to perform necessary computations and interpret graphs.
• Working knowledge of instrumentation software used in laboratories.

About the Role

We are seeking a dedicated Associate Scientist to perform routine tests on various samples, including finished products, stability samples, and raw materials, using techniques such as UV and HPLC in a regulated laboratory environment. This role involves evaluating test results, maintaining accurate lab documentation, and ensuring compliance with SOPs and cGMP standards.