Director, Global Audit
At Alcon, we are driven by the meaningful work we do to help people see brilliantly. We innovate boldly, champion progress, and act with speed as the global leader in eye care. Here, you’ll be recognized for your commitment and contributions and see your career like never before. Together, we go above and beyond to make an impact in the lives of our patients and customers.
We foster an inclusive culture and are looking for diverse, talented people to join Alcon. As a Director, Global Audit supporting Quality Assurance Compliance, you will be trusted to assist in the development and management of the corporate audit program at Fort Worth, TX.
In this role, a typical day will include:
If you are currently an active employee/contingent worker at Alcon, please click the appropriate link below to apply on the Internal Career site.
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Alcon is an Equal Opportunity Employer and participates in E-Verify. Alcon takes pride in maintaining a diverse environment and our policies are not to discriminate in recruitment, hiring, training, promotion or other employment practices for reasons of race, color, religion, gender, national origin, age, sexual orientation, gender identity, marital or veteran status, disability, or any other legally protected status. Alcon is also committed to working with and providing reasonable accommodation to individuals with disabilities. If, because of a medical condition or disability, you need a reasonable accommodation for any part of the application process, or in order to perform the essential functions of a position, please send an email to alcon.recruitment@alcon.com and let us know the nature of your request and your contact information.
We foster an inclusive culture and are looking for diverse, talented people to join Alcon. As a Director, Global Audit supporting Quality Assurance Compliance, you will be trusted to assist in the development and management of the corporate audit program at Fort Worth, TX.
In this role, a typical day will include:
- Plan, schedule, and implement internal and external GMP/PV audits with a primary focus on manufacturing site audits, including unplanned/for-cause/focused audits.
- Lead and/or implement global audit-based projects; and act as global audit SME for audit QMS and management assigned topics.
- Conduct detailed global corporate audits on Alcon or contracted medical device and pharmaceutical manufacturers. Assigned audits may also include contract laboratories, suppliers, service providers, vigilance operations, distribution centers, and affiliates.
- Represent Alcon audit function in external industry and health authority working teams and related conferences and workshops as appropriate.
- Facilitate between site internal auditor community and corporate audit team to drive consistent implementation of identified projects & improvements across corporate/site internal/supplier external audits.
- Provide objective written audit reports in a timely manner for audit targets based on regulatory and Alcon corporate requirements as well as internal needs; work with auditees to ensure proper and effective CAPAs.
- Perform focused or for-cause site audits as needed by Quality Management
- Develop and deliver training on audit-related topics to global audit or community.
- Act as internal group SME for HA/NB audit trends and SME for assigned gap assessments for regulation changes and other topics as assigned by management.
- Provide global audit consultation and compliance mentorship, to sites as needed. Coordinating with manufacturing management to establish practices and procedures that apply to applicable regulations.
- Review regulatory requirements, standards, and inspection trends for incorporation into Alcon audit procedures and practices and give feedback to the wider audit community.
- Follow all applicable company procedures and policies, cGMPs, and any other applicable external quality and regulatory requirements.
- Bachelor’s Degree or Equivalent years of directly related experience (or high school +18 yrs.; Assoc.+14 yrs.; M.S.+7 yrs.; PhD+6 yrs.)
- The ability to fluently read, write, understand, and communicate in English
- 10 Years of Relevant Experience
- 6 Years of Demonstrated Leadership
- Travel Requirements: 50%
- Relocation assistance: Yes
- Sponsorship available: No
- Medical Device and/or Pharmaceutical Manufacturing experience preferred.
- Collaborate with teammates to share standard processes and findings as work evolves
- See your career like never before with focused growth and development opportunities
- Join Alcon’s mission to provide outstanding, innovative products and solutions to improve sight, improve lives, and grow your career!
- Alcon provides a robust benefits package including health, life, retirement, flexible time off for exempt associates, PTO for hourly associates, and much more!
If you are currently an active employee/contingent worker at Alcon, please click the appropriate link below to apply on the Internal Career site.
Find Jobs for Employees
Find Jobs for Contingent Worker
Alcon is an Equal Opportunity Employer and participates in E-Verify. Alcon takes pride in maintaining a diverse environment and our policies are not to discriminate in recruitment, hiring, training, promotion or other employment practices for reasons of race, color, religion, gender, national origin, age, sexual orientation, gender identity, marital or veteran status, disability, or any other legally protected status. Alcon is also committed to working with and providing reasonable accommodation to individuals with disabilities. If, because of a medical condition or disability, you need a reasonable accommodation for any part of the application process, or in order to perform the essential functions of a position, please send an email to alcon.recruitment@alcon.com and let us know the nature of your request and your contact information.
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Seniority level
Director -
Employment type
Full-time -
Job function
Accounting/Auditing and Finance -
Industries
Medical Equipment Manufacturing
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