Job Details
Skills And Tools:
Job Description
Develop, implement, and update the Validation Master Plan (VMP) for the site.
Plan, prepare, and execute validation and qualification protocols in compliance with GMP and regulatory requirements.
Ensure proper documentation, reporting, and audit readiness for all validation activities.
Conduct risk assessments and propose improvements to maintain compliance and efficiency.
Collaborate with QA, QC, R&D, Manufacturing, and Engineering to support new projects and ongoing operations.
Investigate validation-related deviations and oversee CAPA (Corrective and Preventive Actions).
Provide training and guidance to staff on validation practices and standards.
Qualification:
Bachelor’s degree in Pharmaceutical Engineering, Chemical Engineering, Biotechnology, or related field.
5+ years of experience in pharmaceutical, veterinary, or feed manufacturing validation.
Strong knowledge of GMP, ISO, and international validation guidelines (EU/FDA/WHO).
Broad understanding of equipment, process, cleaning, computer system, and method validation.
Excellent documentation and communication skills.
