Company Description AbbVie's mission is to discover and deliver innovative medicines and solutions 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, and eye care – and products and services in our Allergan Aesthetics portfolio. For more information about AbbVie, please visit us at www.abbvie.com. Follow @abbvie on X, Facebook, Instagram, YouTube, LinkedIn and Tik Tok (https://www.tiktok.com/@abbvie) . Job Description Join our dynamic Validation Department at AbbVie Westport and make a significant impact on the pharmaceutical industry. As a Pharmaceutical Technology Specialist III, you'll play a vital role in ensuring the quality and compliance of our manufacturing processes. Your expertise will be instrumental in validating and revalidating critical equipment, systems, and processes to meet stringent regulatory standards. Are you passionate about delivering high-quality products? If so, this is the perfect opportunity to contribute to our mission of providing exceptional healthcare solutions. The Validation Department is responsible for the qualification / validation of all CGMP equipment, systems and processes utilized for routine operation at the Allergan Westport manufacturing site. The Department is also responsible for the revalidation of critical systems & processes. The role of the Pharmaceutical Technology Specialist III is to ensure customer satisfaction is delivered with each, revalidation, validation and project work. All Validation activity is to be performed in line with Global Standards, FDA, HPRA and other MOH regulatory requirements. This schedule compliance will be achieved by actively engaging with senior management and the impacted BU’s and ensuring all projects can be managed and prioritized as required. This role involves overseeing and implementing a validation master plan to ensure all processes and equipment meet regulatory standards. It includes: + Project Management: Managing validation projects, reviewing and approving documentation, and coordinating with other engineers. + Regulatory Compliance: Staying up-to-date on industry regulations and supporting audits. + Quality Assurance: Ensuring compliance with EHS requirements and quality standards. + Documentation: Maintaining accurate and organised documentation for validation studies. + Teamwork: Collaborating with other validation engineers to achieve project goals. Qualifications + Bachelor’s degree required in science based or engineering discipline + Experience in Pharmaceutical company + Excellent project management skills + Proficient in use of Microsoft Office suite of programs + Critical Thinking and Problem Solving skills Additional Information Interested? Apply today and be part of groundbreaking work that transforms lives. AbbVie is an equal opportunity employer and is committed to operating with integrity, driving innovation, transforming lives, serving our community and embracing diversity and inclusion. It is AbbVie’s policy to employ qualified persons of the greatest ability without discrimination against any employee or applicant for employment because of race, color, religion, national origin, age, sex (including pregnancy), physical or mental disability, medical condition, genetic information, gender identity or expression, sexual orientation, marital status, status as a protected veteran, or any other legally protected group status. US & Puerto Rico only - to learn more, visit https://www.abbvie.com/join-us/equal-employment-opportunity-employer.html US & Puerto Rico applicants seeking a reasonable accommodation, click here to learn more: https://www.abbvie.com/join-us/reasonable-accommodations.html