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Bioequivalence In-vivo Lab Analyst at MARC
6th of October, Giza, Egypt -
Full Time

Start Date

Immediate

Expiry Date

11 May, 26

Salary

0.0

Posted On

10 Feb, 26

Experience

0 year(s) or above

Remote Job

Yes

Telecommute

Yes

Sponsor Visa

No

Skills

Bioanalytical Method Development, Validation, In-vivo Sample Analysis, LC-MS/MS, SOP Compliance, GLP Compliance, Regulatory Guidelines, Equipment Calibration, Sample Processing, Data Accuracy, Traceability, Data Integrity, ALCOA+

Industry

Research Services

Description
MARC for Medical Services and Scientific Research is an integrative research center that aims to advance science by conducting research in interdisciplinary disease areas. Our goal is to conduct high-priority and ethical basic, preclinical and clinical research, bridging the gap between science and community to improve health and quality of life. MARC is looking to have an experienced candidate for Bioequivalence In-vivo Lab Analyst Key responsibilities: Perform bioanalytical method development, validation, and in-vivo sample analysis using LC–MS/MS in compliance with SOPs, GLP, and regulatory guidelines. Ensure proper equipment calibration, maintenance, and documentation in accordance with GLP. Prepare and process samples and reagents while ensuring data accuracy, traceability, and integrity per ALCOA+ principles. Bachelor’s degree in science or pharmacy 1–3 years of experience in a bioanalytical laboratory. At least one year of hands-on experience with LC–MS/MS and bioanalytical method development and validation Ability to perform routine bioanalytical analysis.
Responsibilities
The main responsibilities involve performing bioanalytical method development, validation, and in-vivo sample analysis utilizing LC-MS/MS, all while strictly adhering to SOPs, GLP, and regulatory guidelines. This includes ensuring proper equipment maintenance and preparing/processing samples to maintain data accuracy and integrity.