Bioanalyst - LC-MS/MS Method Validation (Clinical Trials)

Farmovs; Bloemfontein; On-site; ZAR 550,000 - 900,000; Full time

Benefits offered by this job

Competitive salary

Benefits package

Equal opportunity employer

Job summary

FARMOVS seeks a Bioanalyst to join the chemical laboratory team, developing and validating bioanalytical methods and analysing biological samples for clinical trials. You will work with LC-MS/MS and HPLC equipment, ensuring data meets regulatory standards and scientific excellence.

The role involves meticulous documentation, calibration of instruments, and active participation in audits within a dynamic clinical research setting in Bloemfontein.

Qualifications

• Degree in a relevant science with a focus on bioanalytical work and regulatory awareness.
• Minimum 3 years’ experience in a bioanalytical or chemical lab, CRO or regulated env.
• Proven experience in method validation for clinical or preclinical studies.
• Strong knowledge of LC-MS/MS and HPLC with regulatory understanding.

Responsibilities

• Perform quantitative and qualitative bioanalytical tests on biological matrices using LC-MS/MS.
• Develop and validate bioanalytical methods in compliance with regulatory guidelines.
• Review and interpret analytical data, troubleshoot issues, and ensure accuracy of results.
• Document and report analytical findings with meticulous records.
• Ensure laboratory equipment is calibrated, maintained, and functioning optimally.
• Participate in audits and ensure compliance with quality systems and safety protocols.

Skills

LC-MS/MS

HPLC

Bioanalytical methods

GLP/FDA/ICH

Analytical skills

Communication

Education

BSc (Hons) or MSc in Chemistry, Biochemistry, Pharmaceutical Sciences or related field; Diploma considered

Tools

Analyst

SCIEX OS

MassLynx

Chemstation

MassHunter

Watson LIMS

Job description

FARMOVS seeks a Bioanalyst to join the chemical laboratory team, developing and validating bioanalytical methods and analysing biological samples for clinical trials. You will work with LC-MS/MS and HPLC equipment, ensuring data meets regulatory standards and scientific excellence.

The role involves meticulous documentation, calibration of instruments, and active participation in audits within a dynamic clinical research setting in Bloemfontein.