AbbVie is a global biopharmaceutical company committed to discovering and delivering innovative medicines and solutions that address serious health issues today and in the future. We operate in several key therapeutic areas, including immunology, oncology, neuroscience, and eye care, as well as our Allergan Aesthetics portfolio.
Job Description
We are seeking an experienced Maintenance Lead to join our engineering team in Sligo, Ireland. This role will report directly to the API Engineering Manager and involve leading and managing a team of plant support engineers and technicians to ensure manufacturing operations run continuously, efficiently, and effectively.
Responsibilities
* Ensure seamless continuity across shifts throughout the week, including morning handovers.
* Complete timecard reviews and approvals for all Plant Support Engineers.
* Oversee adherence to training schedules, deliver toolbox talks, coordinate work orders, and conduct work order reviews.
* Conduct weekly reviews to ensure accuracy and completeness of Production History (PH) sheets.
* Arrange shift coverage for annual leave, approve annual leave requests, and handle other employee requests.
* Set performance goals, manage performance development activities, and provide feedback for direct reports.
* Participate in weekly planning meetings to discuss ongoing projects and priorities.
* Represent the engineering team at Tier 1 morning meetings to ensure effective communication.
* Resolve manufacturing escalations promptly and efficiently.
* Coordinate resources, assign tasks, and oversee project activities.
* Collaborate closely with Technical Shift Leaders and Operations Supervisors to ensure interdepartmental activities are planned and executed safely.
* Ensure compliance with all safety, environmental, and quality-related Business Operating Procedures (BOPs).
* Maintain accurate documentation of all activities in accordance with current Good Manufacturing Practices (cGMP) regulations.
* Cross-train team members, train new hires, and maintain overall cGMP standards in pharmaceutical processing areas.
Requirements
* Diploma or trade qualification in a suitable science or engineering field, or equivalent experience.
* At least 3 years' experience in a highly regulated industry performing a similar role.
* In-depth functional knowledge of a wide range of manufacturing equipment is essential.
* Proven ability to troubleshoot instrumentation issues.
* Strong understanding of procedures, policies, and guidelines required to comply with cGMP and regulatory guidelines.
* Flexibility to work varying shifts, including weekends, and adhere to a standby schedule.
About AbbVie
AbbVie is an equal opportunity employer committed to operating with integrity, driving innovation, transforming lives, serving our community, and embracing diversity and inclusion. We strive to create a workplace where everyone feels valued, respected, and empowered to contribute their best work.