Analytical Method Validation Specialist

We are seeking an experienced Analytical Method Validation Specialist to support Quality Control (QC) Operations within a leading pharmaceutical manufacturing environment. The successful candidate will be responsible for coordinating and authoring analytical method validation activities, ensuring compliance with GMP requirements and supporting continuous improvement initiatives. This role offers the opportunity to work closely with laboratory teams, statisticians, quality representatives, and project stakeholders while contributing to critical validation projects and quality excellence programs. Key Responsibilities Analytical Method Validation Documentation

• • Author and maintain validation-related documentation including:
• • Validation protocols

• Validation reports

• Amendments

• Risk assessments

• Scientific rationale reports

• Technical instructions

• Periodic review documentation

• Raw data review documentation

• Comparability protocols and reports

• QC material qualifica…