Allergan Validation Engineer in Mayo, United States

Validation Engineer

Mayo, Connaught, Ireland at

Oct 26, 2018Post Date

184506Requisition #

  • Updating Validations SOPS and Masters Plans to ensure compliance to current and future EU/FDA regulations.

  • Maintaining an up to date knowledge of relevant regulatory requirements. Interact with other departments to ensure that validation projects are appropriately planned, executed and delivered in a timely manner.

  • Approval of SDLC documentation in line with current regulatory and corporate requirements.

  • Minimum 3rd level Science /Engineering degree. Minimum 2 years’ experience working in a Validations environment.

  • Comprehensive understanding of Validation principles and practices.

  • Very good working knowledge of Validations practices, ASTM and relevant EU/FDA regulations.

  • A proven track record that demonstrates the ability to work without direct supervision whilst maintaining adherence to project delivery is fundamental to the role.

Equal Employment Opportunity Employer

Allergan is an equal opportunity employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, protected veteran status, disability, or any other protected status.