Advance your career in validation engineering with our client's pharmaceutical manufacturing team located in Kimberley. Focus on the validation of critical processes and equipment to comply with regulatory standards. The ideal candidate for this Validation Engineer role will possess a meticulous approach to validation in the pharmaceutical sector.
Key responsibilities include developing validation protocols, ensuring adherence to cGMP, and troubleshooting potential validation issues. This opportunity is perfect for those with a strong validation background looking to make a significant impact in Northern Cape. Key Responsibilities:
- Develop validation protocols for manufacturing and utilities
- Review and ensure compliance of validation reports
- Collaborate across engineering, manufacturing,
and QA teams
- Maintain equipment validation through systematic processes
- Troubleshoot validation issues affecting production Requirements:
- Bachelor's degree in Engineering or similar
- At least 3 years of validation engineering experience
- Comprehensive understanding of cGMP and related guidelines
- Experience in qualifying various pharmaceutical equipment
- Solid writing and project management capabilities Contribute your expertise in validation to enhance product quality and safety for essential pharmaceuticals in Kimberley.