Director, GCP & Lifecycle Quality Assurance

Alcon

Lake Forest (CA)

On-site

USD 184,000 - 238,000

Full time

7 days ago

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Benefits offered by this job

Health benefits

Life insurance

Retirement plan

Flexible time off

Job summary

Alcon is seeking a Director of Good Clinical Practices (GCP) and Lifecycle Management in Fort Worth, TX, to lead the Quality & Regulatory Affairs function. You will guide a team, drive regulatory adherence, and oversee clinical trial quality programs.

Responsibilities include strategic direction, cross-functional collaboration, and ensuring compliance across product lifecycle. Onsite role with 20% travel, relocation assistance available, sponsorship none.

Qualifications

Bachelor's degree or equivalent years of related experience.
English reading, writing, understanding and communication essential.
10 years of relevant experience and 6 years of demonstrated leadership required.

Responsibilities

Provide leadership and strategic direction to multiple teams for departmental plans and objectives.
Oversee team performance, resource allocation, and project approvals while fostering compliance.
Oversee multiple teams, implementing departmental plans.
Drive cross-functional quality culture and ensure QMS at every stage of processes.
Make key decisions impacting significant projects and initiatives.
Implement quality plans at every stage of the Clinical Trial process and ensure compliance.
Support audits, regulatory inspections, and quality control activities.