Analyst - In Vitro

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1. Conduct or support one or more of the following:

• In vitro release testing (IVRT) and in vitro permeation testing (IVPT) for pharmaceutical formulations.
• In vitro bioequivalence studies and BCS biowaiver studies as per regulatory standards.
• Enteral feeding tube studies to assess drug administration compatibility.
• Analysis and interpretation of data from in vitro studies, applying statistical methods where required.

1. Ensure compliance with FDA, EMA, ICH, and USP guidelines in laboratory procedures.
2. Prepare and review study protocols, scientific reports, and regulatory documentation.
3. Collaborate with cross-functional teams, including regulatory affairs and bioanalytical scientists.
4. Maintain laboratory equipment, follow SOPs, and ensure GLP/GMP compliance.
5. Basic understanding of statistical analysis for in vitro studies is a plus.

• Education: Bachelor s, Master s or Ph.D. in Pharmaceutical Sciences, Biopharmaceutics, Analytical Chemistry, or a related field.
• Experience: At least 2 years of experience in any in vitro research area, preferably within a CRO or pharmaceutical company.

• Strong analytical and problem-solving abilities.
• Excellent written and verbal communication skills.
• Ability to learn quickly and adapt to new in vitro methodologies.

• Work with a leading CRO specializing in diverse in vitro research areas.
• Gain exposure to multiple in vitro techniques and expand your expertise.
• Collaborative and growth-oriented work environment.