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