Manufacturing Technician (Documentation Support)

About AbbVie 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 including immunology, oncology and neuroscience, as well as products and services in our Allergan Aesthetics portfolio. Role Overview We are inviting experienced and driven candidates to apply for the Manufacturing Technician (Documentation Support) position at AbbVie Westport. In this role, you will ensure the continued success of our Biologics 2 business unit by taking ownership of various duties relating to CAPA and continuous improvement, documenting batch‑related activities, housekeeping, and aseptic manufacturing. Key Responsibilities Carry out daily tasks as assigned by the Senior Operations Manager according to GMP and the quality system. Active involvement and management of batch‑related CAPA’s as they arise in the business unit, taking them from the initial review state through RCA, approval, batch disposition, and delivery of corrective and preventive actions; liaising closely with the relevant Departments to ensure thorough investigation and timely resolution and closure. Assist in the management and closure of existing CAPA’s through the evaluation of the current status of corrective and preventive action, including interdepartmental coordination to ensure robust actions are in place to prevent reoccurrence prior to closure. Lead and support continuous improvement initiatives as required to support the overall goals of the Biologics 2 Process Team. Based on knowledge and previous experience, facilitate, support and generate RCA reports. Participate in GNEMBA’s and Process Confirmations to identify further improvement opportunities within the department. Manage requirements to deliver the KPIs related to the Product Flow function with specific emphasis on the batch release cycle. Participate in root‑cause analysis and problem‑solving. Complete compliant investigations and environmental excursions. Adhere to all company standards in safety, housekeeping, and quality, notifying management of any discrepancies. Follow gowning procedures on entry to areas. Adhere to and support all EH&S standards, procedures, and policies. Qualifications Leaving cert or equivalent qualification required. Third‑level qualification in science or engineering a advantage but not essential. Understanding of requirements to work in a regulated GMP industry. Ability to build strong relationships and work within cross‑functional teams. Adaptability to work in a fast, dynamic environment whilst adjusting readily to meet unexpected constraints. Drive, high energy, maturity, and ability to work under pressure, deliver results, and overcome obstacles. Team player who can collaborate with others to achieve organizational targets and goals. Knowledge of biologics operations is an advantage. Excellent communication skills. Equal Opportunity Statement AbbVie is an equal opportunity employer and is committed to operating with integrity, driving innovation, transforming lives, and serving our community. Equal Opportunity Employer/Veterans/Disabled. US & Puerto Rico only. #J-18808-Ljbffr