AbbVie, a global leader in innovative pharmaceutical solutions, is seeking an experienced Operations Shift Supervisor for our Drug Product Manufacturing facility in Sligo. This full-time supervisory role offers the opportunity to lead pharmaceutical production operations while ensuring the highest standards of quality, safety, and regulatory compliance.
About the Role
Join AbbVie’s Drug Product Manufacturing team as an Operations Shift Supervisor, where you’ll oversee the safe and compliant production of life-changing medicines. This key leadership position involves managing a team of 10-12 pharmaceutical technicians while driving continuous improvement in our state-of-the-art Sligo facility. You’ll play a crucial part in maintaining AbbVie’s reputation for excellence in pharmaceutical manufacturing.
Key Responsibilities
- Supervise pharmaceutical processing activities to meet operational objectives and production targets in Drug Product Manufacturing
- Lead and develop a team of 10-12 direct reports, ensuring clear communication of tasks, goals, and safety protocols
- Plan resources and coordinate training to maintain safe, efficient operations in compliance with cGMP standards
- Monitor and report key performance metrics including yield rates, production efficiency, usage metrics, and team performance
- Ensure strict compliance with all safety, environmental, quality SOPs, and FDA/HPRA regulatory requirements
- Collaborate with shift supervisors and cross-functional stakeholders to optimize interdepartmental Drug Product operations
- Manage employee relations and development, conducting performance reviews and creating growth plans with HR partnership
- Maintain accurate manufacturing records and update control systems for batch processing documentation
- Support implementation of key site strategies and departmental continuous improvement initiatives
- Lead regulatory compliance during FDA, HPRA, and other regulatory inspections and audits
- Drive innovation and problem-solving to enhance Drug Product Manufacturing efficiency and quality
Required Qualifications
Essential Requirements
- Diploma in science or engineering discipline, or equivalent pharmaceutical manufacturing experience
- Minimum 3 years’ experience in batch processing operations within FDA/HPRA regulated pharmaceutical environment
- Comprehensive knowledge of cGMP and pharmaceutical regulatory requirements
- Minimum 3 years’ experience in highly automated pharmaceutical manufacturing environment
- Minimum 3 years’ direct supervisory experience or equivalent leadership training in manufacturing operations
- Proven track record leading teams and participating in continuous improvement programs
Preferred Qualifications
- Advanced degree in pharmaceutical sciences, chemical engineering, or related field
- Experience in Drug Product Manufacturing specifically (tablets, capsules, sterile products)
- Six Sigma or Lean Manufacturing certification
- Experience with regulatory inspections and audit management
- Project management skills and change management experience
What We Offer
- Competitive salary commensurate with experience in pharmaceutical manufacturing supervision
- Comprehensive benefits package including health insurance, pension, and life insurance
- Professional development opportunities including technical training and leadership development programs
- Career advancement potential within AbbVie’s global pharmaceutical operations network
- Flexible working arrangements to support work-life balance, including shift pattern flexibility
- State-of-the-art facilities with cutting-edge pharmaceutical manufacturing technology
- Opportunity to impact lives through involvement in producing life-changing medicines
Ready to Apply?
Join AbbVie’s mission to discover and deliver innovative medicines that solve serious health issues. If you’re ready to lead a high-performing Drug Product Manufacturing team in a world-class pharmaceutical environment, we want to hear from you.
