QC Validation Scientist – Relocation Provided

CordenPharma International; North Augusta (SC); On-site; USD 70,000 - 110,000; Full time

Benefits offered by this job

Relocation assistance

Job summary

CordenPharma International in North Augusta, SC seeks a QC Validation Scientist to validate analytical testing methodologies for raw materials, intermediates, and finished products. Relocation assistance is provided for candidates willing to relocate to the area.

Responsibilities include method transfer/verification/validation using HPLC/UPLC/GC, KF, and spectroscopy, adhering to GMP SOPs, and preparing validation reports.

Qualifications

• Bachelor or Master’s degree in Chemistry, life sciences, or related discipline.
• 5–7 years bench experience for Bachelor’s degree and 4–6 years for Master degree in a QC laboratory.
• Proficiency in MS Word and MS Excel.

Responsibilities

• Safely and effectively validate analytical testing methodologies for raw materials, intermediates, and final products.
• Perform transfer/verification/validation of test methods using HPLC, GC, KF, spectroscopy, and wet chemical testing.
• Investigate and resolve analytical issues within Analytical Development, method validation, and QC.
• Follow SOPs for Good Manufacturing Practices and prepare/ review technical documentation and validation reports.
• Identify out-of-specification results and report non-routine analytical problems.
• Maintain and troubleshoot analytical instrumentation; support method optimization and transfer.

Skills

Strong analytical skills

Excellent writing skills

MS Word / Excel proficiency

Education

Bachelor or Master in Chemistry or life sciences

Tools

HPLC

UPLC

GC

KF

Spectroscopy

LCMS

UHPLC

Job description

CordenPharma International in North Augusta, SC seeks a QC Validation Scientist to validate analytical testing methodologies for raw materials, intermediates, and finished products. Relocation assistance is provided for candidates willing to relocate to the area.

Responsibilities include method transfer/verification/validation using HPLC/UPLC/GC, KF, and spectroscopy, adhering to GMP SOPs, and preparing validation reports.