NPI Engineering Team Lead – Medical Devices
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Sligo, SO
- Operations
- On-Site
- Full-time
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 - and products and services in our Allergan Aesthetics portfolio. For more information about AbbVie, please visit us at www.abbvie.com. Follow @abbvie on LinkedIn, Facebook, Instagram, X and YouTube.
We are seek an NPI Engineering Team Lead – Medical Devices to join our Engineering Team in Ballytivnan. In this role,you will lead a team of engineers and technicians responsible for introducing new medical device products, technologies, equipment, materials, and manufacturing processes.
You will work closely with Operations, Quality, Maintenance, EHS, suppliers, and cross-functional project teams to deliver projects from concept through design, commissioning, validation, and handover to production.
Key Responsibilities
- Lead and develop the NPI engineering team, supporting capability building and technical development.
- Manage new product introduction projects to meet quality, budget, schedule, and compliance requirements.
- Provide technical leadership in injection moulding, automated assembly, tooling, equipment, and process development.
- Support equipment and process trials, troubleshooting, qualification, and validation activities.
- Introduce and optimise manufacturing technologies, automation, and ancillary equipment.
- Partner with Operations to improve yield, downtime, equipment performance, and production delivery.
- Work with equipment suppliers and cross-functional teams to resolve technical issues.
- Support knowledge transfer, training, continuous improvement, and Maintenance Excellence initiatives.
- Ensure documentation and activities comply with cGMP, ISO, FDA, EHS, and site requirements.
- Level 7 qualification or higher in Engineering or a related technical discipline.
- At least three years’ experience in a high-precision manufacturing environment.
- At least two years’ experience in regulated manufacturing.
- Strong experience in injection moulding, including process setup, development, debugging, and validation.
- Experience with medical device components, automated assembly, tooling, and equipment introduction.
- Knowledge of thermoplastics, cleanroom manufacturing, and validation documentation.
- Proven ability to lead teams and work effectively with cross-functional stakeholders.
- Strong problem-solving, communication, organisational, and decision-making skills.
- Commitment to quality, compliance, safety, and Right First Time principles.
Desirable: Experience with PLC programming, Lean or SMED methodologies, statistical analysis, Microsoft Project, and Maintenance Excellence programmes.
Closing Date: Friday 11th September
This is a site based role
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 - 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
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Where We Work
Role is exclusively performed at a site or office and onsite presence is required. Employees who are site/office-based and can occasionally perform their role virtually work both in the office and remotely*, following the policies and regulations in place at their location. US Employees must be in the office on Tuesday, Wednesday, and Thursday with flexibility to work remotely on Mondays and Fridays. Three days in the office is the minimum; some individuals or teams may require more in-office days due to meetings, business/project needs or their role.