Skip to main content

Search jobs

Search jobs

About AbbVie

AbbVie’s mission is to discover and deliver innovative medicines that solve serious health issues today and address the medical challenges of tomorrow. We strive to have a remarkable impact on people’s lives across several key therapeutic areas: immunology, oncology, neuroscience, eye care, virology, women’s health and gastroenterology, in addition to products and services across its Allergan Aesthetics portfolio. For more information about AbbVie, please visit us at www.abbvie.com. Follow @abbvie on Twitter, Facebook, Instagram, YouTube and LinkedIn.

Validation Engineer

Sligo, Ireland Req ID 2119492 Category Quality Assurance Division AbbVie

Want to make a global impact? We offer that.

Want to be part of a Great Place to Work in Ireland? We offer that too.
 

We are a global, research-based biopharmaceutical company that combines the focus and passion of leading-edge biotech with the expertise and capability of an established pharmaceutical leader. Redefining what is possible is our business and our passion. Our goal is to help patients live healthier lives and we are proud to be a Great Place to Work.
 
We are recruiting for a Validation Engineer to join our team at our Manorhamilton Road site in Sligo. Reporting directly to the Validation Team Lead, you will be responsible for coordinating the development and maintenance of the company’s validation program in compliance with all applicable regulatory and company requirements.

Are you intrigued? Do you want to learn more?

A snapshot of your key responsibilities as Validation Engineer would be:

  • Ensure all computerised systems are qualified in compliance with Data Integrity policies and regulatory requirements.
  • Co-ordination / direction and active participation in the validation of site equipment, facilities, utilities, processes and software in compliance with company policies, FDA, European cGMP and GAMP standards.
  • Generation/maintenance of the Validation Master Plans.
  • Generation of validation plans, protocols and final reports to cGMP standard.
  • Review / approval of all protocols and final reports.
  • Management of validation change control process.
  • Adheres to and supports all EHS & E standards, procedures and policies
  • Adheres to and follows all procedures policies and guidelines ensuring compliance with cGMP and HPRA/FDA regulations and company policies, procedures and guidelines.
  • Close contact with internal and external auditors, e.g. FDA, HPRA.
     
Qualifications:

Education and Experience;

  • 3rd level qualification in a relevant engineering or scientific discipline.
  • A minimum of 2 years’ experience in a cGMP regulated environment.
  • A good understanding of regulatory requirements.
     
Travel: No
Job Type: Experienced
Schedule: Full-time
ABBVIE

Most recent jobs

Sign up for job alerts

Join our talent network and receive AbbVie news and job alerts to your inbox.

Interested InPlease select a category or location option. Click “Add” to create your job alert.

Our Terms of Use, Cookie Policy and Privacy Policy explain how we collect and use information about you and the rights you have. By submitting your information, you acknowledge you have read those documents and consent to receive SMS communications and email jobs alerts from AbbVie.

Recently viewed jobs

You have not viewed any jobs recently.

Phishing scam alert

As an online job seeker, you could be a target of cyber (online) thieves seeking to secure personal information from you by sending you “phishing” messages.

Please be alert to and protect yourself from phishing scams. Find out how you can avoid being a victim of job phishing scams.

For Internal Candidates only - Notice of Filing of Labor Condition Application

Equal Employment Opportunity | Reasonable Accommodation