Our client is looking for a meticulous Validation Engineer to join their technical operations team in Paarl . This role is essential for ensuring that all pharmaceutical manufacturing equipment, utilities, and processes meet stringent regulatory requirements and are fit for their intended purpose. You will be responsible for developing and executing validation protocols, maintaining validation documentation, and ensuring compliance with GMP standards. This position is critical to maintaining the integrity and quality of pharmaceutical production, offering a stable and important role within the manufacturing sector.
Key Responsibilities
Develop, execute, and document validation protocols (IQ, OQ, PQ) for pharmaceutical manufacturing equipment and systems.
Ensure all validation activities comply with GMP, FDA, and other relevant regulatory guidelines.
Maintain validation documentation, including validation master plans and reports.
Troubleshoot and resolve issues related to equipment qualification and validation.
Collaborate with engineering, manufacturing, and quality assurance teams to support validation efforts.
Requirements
Bachelor's degree in Engineering (Mechanical, Electrical, Chemical) or a related technical field.
Minimum of 2 years of experience in validation engineering within the pharmaceutical or biopharmaceutical industry.
Thorough understanding of GMP and validation principles (IQ/OQ/PQ).
Experience with qualification of process equipment, utilities, and analytical instruments.
Strong technical writing and documentation skills.
Benefits
Competitive salary based on experience and qualifications.
Comprehensive medical aid and retirement fund.
Professional development opportunities and training in validation methodologies.
A well-equipped facility in Paarl with opportunities to work with modern pharmaceutical technology.
A collaborative environment focused on ensuring product quality and regulatory compliance.
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Validation Engineer - Pharmaceutical Equipment • Paarl, Western Cape, ZA