Validation Engineer - Katalyst Healthcares and Life Sciences : Job Details

Job Summary The Validation Engineer is responsible for executing equipment and system validation activities within a regulated biopharmaceutical environment. This role involves implementing validation protocols, documenting results, and ensuring compliance with regulatory requirements. The position is based in West Philadelphia, Pennsylvania with a hybrid work arrangement. Responsibilities:

• Proficiency in Kaye AVS validation software.
• Experience with Valpro validation management systems.
• Competence in Kneat Veeva validation documentation platform.
• Expertise in temperature excursion analysis and mitigation.
• Validation protocol execution and documentation.
• Regulatory compliance management.

Requirements:

• Minimum 3+ years of relevant validation engineering experience.
• Experience in biopharmaceutical industry preferred.
• Demonstrated expertise with validation software platforms (Kaye AVS, Valpro, Kneat Veeva).
• Proven capability in temperature exercising validation activities.
• Knowledge of cGMP requirements and regulatory standards.