AbbVie is recruiting a DP Operations Shift Supervisor at its pharmaceutical manufacturing facility in Sligo, County Sligo. This is a senior leadership opportunity within a world-class, FDA/HPRA-regulated production environment, offering real scope to shape team performance, drive continuous improvement, and contribute directly to the manufacture of life-changing medicines.
About the Role
Reporting to the DP Operations Leader, the Shift Supervisor oversees the safe, compliant, and efficient production of drug product materials on shift. Operating with a high degree of autonomy, you will lead a team of up to nine pharmaceutical technicians, manage departmental performance metrics, and act as a Subject Matter Expert for drug product manufacturing issues. You will also represent your area during regulatory inspections and audits, making this a highly visible and impactful role within the site.
Key Responsibilities
- Supervise and execute pharmaceutical processing activities to meet operational objectives on shift.
- Lead, motivate, and develop a team of 4–9 direct reports, ensuring clear communication of tasks, priorities, and goals.
- Plan and coordinate resources and training schedules to maintain safe and efficient operations.
- Measure, report, and take ownership of key departmental performance metrics including yield, rate, material usage, attendance, and overtime.
- Ensure full compliance with all safety, environmental, and quality SOPs in line with cGMP and regulatory requirements.
- Collaborate with other shift supervisors and internal and external stakeholders to ensure smooth interdepartmental operations.
- Manage employee relations, conduct performance reviews, and develop individual growth plans in partnership with HR.
- Maintain accurate personnel records and update manufacturing control systems.
- Support and implement key site and departmental strategic initiatives.
- Lead and participate in continuous improvement programmes across the department.
- Set annual goals and provide technical leadership as site SME for DP manufacturing.
- Represent the department during regulatory inspections and audits.
Requirements
- Level 8 qualification in a relevant science or engineering discipline.
- Minimum 3 years’ experience in batch processing operations within an FDA/HPRA-regulated pharmaceutical environment.
- Detailed knowledge of cGMP and applicable regulatory requirements.
- At least 3 years’ experience working in a highly automated manufacturing environment.
- Minimum 3 years’ direct supervisory experience or equivalent relevant training.
- Proven track record of leading teams and contributing to operational improvement programmes.
- High attention to detail with a strong commitment to compliance and a “Right First Time” mindset.
- Strong problem-solving skills with an innovative, results-driven approach.
- Excellent verbal and written communication skills.
- Strong interpersonal and leadership abilities, with demonstrated integrity and work ethic.
- Flexibility to work shift patterns in line with business requirements.
Salary
Competitive pay, commensurate with experience. AbbVie offers a comprehensive benefits package in line with its position as a global pharmaceutical leader.
Location
AbbVie’s Sligo facility is a significant pharmaceutical manufacturing site on the Wild Atlantic Way, operating within a highly regulated, technically advanced production environment. Sligo offers an excellent quality of life, with strong transport links and a growing life sciences community in the North-West.
Contract Type
Full-time, permanent. Shift work is required, including overtime as applicable to business needs.
Application Details
To apply for the DP Operations Shift Supervisor position with AbbVie in Sligo, please submit your application via the Indeed listing linked below.
