Elevate healthcare quality as a Senior Quality Computer Validation Specialist with Mc Kesson. Focus on validation activities for computerized systems and compliance with Gx P standards in this impactful role.In this senior position, you will report to the Senior Manager of Corporate Quality Systems & CSV. Collaborate with multiple business units to ensure adherence to quality standards in validation processes. Support investigations and CAPA activities while mentoring less experienced colleagues to enhance team capabilities.Key Responsibilities:
Support validation activities for computerized systems
Prepare commissioning and qualification documentation
Write and review validation plans and protocols
Maintain quality metrics and implement improvements
Manage training and awareness on validation standardsRequirements:
B. Sc/M. Sc in sciences or IT with 3+ years experience
Knowledge of Canadian GMP requirements
Expertise in validation activities within regulated industries
Solid analytical and communication skills
Ability to work independently on complex projectsDrive impactful change in healthcare quality by leveraging your validation expertise in this vital role at Mc Kesson.#J-18808-Ljbffr