Job Requirements:
- Lead and manage a team of validation professionals, providing guidance and support.
- Foster a culture of collaboration, accountability, and continuous improvement within the CQV team.
- Act as a subject matter expert in CQV activities.
- Develop and execute commissioning, qualification, and validation protocols for manufacturing and laboratory equipment, facilities, utilities, and processes.
- Ensure adherence to AbbVie's validation policies, procedures, and regulatory requirements.
- Identify and mitigate risks associated with CQV activities.
- Develop and implement validation strategies specifically focused on the validation of process equipment, aligned with project timelines and business objectives.
- Collaborate with cross-functional teams to integrate CQV activities into overall project plans.
- Provide input into the development and maintenance of the site validation master plan.
