Operations Leader - Oral Solid Dose Manufacturing

About AbbVie

AbbVie is a globally recognized biopharmaceutical company driven by research and dedicated to pioneering innovative medicines and excellence in pharmaceutical production.

Role Overview

As Operations Leader, you will manage the production of pharmaceutical drug products within a regulated, fast-paced manufacturing environment. This leadership position demands ensuring operational targets, safety compliance, quality standards, and continuous process enhancement are consistently met by the team.

Key Responsibilities

• Manage all aspects of drug product manufacturing operations, aligning with internal protocols and regulatory requirements including cGMP and HPRA/FDA standards.
• Provide leadership, direction, and motivation to a team ranging from 8 to 45 members, promoting communication and personnel development.
• Plan workforce and resources efficiently to maintain seamless, safe daily production activities.
• Coordinate onboarding, training, and ongoing competency development for staff.
• Monitor departmental KPIs such as yield, production throughput, resource utilization, attendance, and overtime.
• Maintain accurate and current documentation within manufacturing and personnel management systems.
• Promote a culture focused on safety, quality, innovation, and ongoing improvement within the manufacturing setting.
• Work closely with fellow shift leaders and cross-functional teams to accomplish operational goals and contribute to site-wide initiatives.
• Lead efforts in facility upgrades, equipment/process enhancements, and Operational Excellence programs.
• Ensure adherence to safety, environmental, and quality SOPs plus all applicable policies and regulations.
• Support human resources activities including performance management, yearly reviews, and employee relations.
• Guide the department through internal and external regulatory inspections and audits.
• Adapt to flexible shift hours and schedules as required by business needs.

Desired Qualifications and Experience

• Experience in pharmaceutical manufacturing, preferably within Oral Solid Dose production.
• Strong leadership capabilities combined with excellent communication and organizational skills.
• Proven track record managing teams and improving operational efficiencies.
• A diploma in a relevant science or engineering field, or significant equivalent industry experience.
• Minimum of three years’ batch processing experience in FDA/HPRA regulated environments with comprehensive knowledge of cGMP and pharma regulations.
• At least three years of supervisory experience in a highly automated manufacturing environment with demonstrated success in process improvement initiatives.
• Exceptional interpersonal skills with a commitment to quality and precision reflected in a 'Right First Time' approach.
• Strong problem-solving skills, a continuous improvement orientation, sound work ethic, and personal integrity.

Additional Information

• Opportunity to work in a cutting-edge pharmaceutical environment with significant impact potential.
• Engage in a team culture emphasising high performance, development, and operational excellence.
• Competitive salary package, comprehensive benefits, and career growth opportunities.

AbbVie maintains a policy of equal opportunity employment committed to integrity, innovation, and community service. Veterans and individuals with disabilities are encouraged to apply.