Freelance Process Validation Engineer

Project Overview:

Join a high-impact containment upgrade project focused on granulation suites within a solid oral dosage manufacturing facility. This is a key role within a multidisciplinary team, supporting critical validation activities from equipment qualification through to final documentation.

Key Responsibilities:

• Develop and execute IQ, OQ, and PQ protocols in line with GMP and regulatory requirements.
• Support the installation and qualification of upgraded containment equipment within granulation processes.
• Interface with engineering, production, and QA teams to ensure seamless execution of validation deliverables.
• Author and review validation reports, risk assessments, and deviation documentation.
• Drive issue resolution and ensure validation milestones are met according to project timelines.

Required Experience:

• 3+ years' experience in validation engineering within pharmaceutical manufacturing (not laboratory-based).
• Strong understanding of solid oral dosage forms, particularly granulation, blending, and tableting processes.
• Proven ability to write and execute IQ/OQ/PQ documentation.
• Familiarity with containment systems and GMP standards in a manufacturing environment.