Senior Pharmaceutical Validation Specialist

Overview

Process Validation Expert – We are seeking a highly motivated and experienced Process Validation Expert to join our team. As a key quality professional, you will be responsible for developing and executing validation protocols in compliance with Good Manufacturing Practices (GMP) standards.

The ideal candidate will have a strong background in Quality Assurance, preferably in the pharmaceutical industry. Your experience in process validation will enable us to ensure that our products meet the highest quality standards.

Key Responsibilities

Develop and execute validation master plans for process and cleaning validation

Prepare validation protocols, reports, and supporting documentation

Ensure validation activities meet GMP requirements and internal quality policies

Collaborate with production, quality control, and engineering teams to implement validation strategies

Perform risk assessments and contribute to corrective action prevention programs

Support site audits and inspections

Contribute to quality system improvements and revalidation of ISO certifications

Requirements

Degree in Pharmacy or Life Sciences

5+ years of experience in pharmaceutical validation, ideally with sterile products

Strong understanding of GMP requirements

Experience with systems like TrackWise, SAP, or similar QMS tools

High level of English proficiency

Excellent attention to detail, technical writing skills, and ability to work collaboratively

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