Associate Director, Specialty Products Printing

Responsibilities

• Lead and oversee a 24/7 multi-shift printing and finishing operation to ensure safety, quality, and productivity targets are achieved.
• Monitor and improve key production metrics (daily, weekly, monthly) and implement process and product improvements.
• Develop, coach, and mentor a large team, including Process Engineers and Shift Leaders, to strengthen technical and leadership capabilities.
• Manage departmental budget, cost controls, and overtime to meet financial and operational targets.
• Partner cross-functionally with support teams to ensure efficient plant operations and alignment with business goals.
• Drive a strong safety culture by analyzing safety data and implementing programs to prevent incidents and lost time accidents.
• Establish and maintain departmental policies, procedures, and standard operating instructions to ensure consistency and compliance.

Requirements

• Bachelor's degree in Engineering or Business Management.
• Proven leadership experience managing teams in a manufacturing or production environment.
• Strong ability to lead large, multi-skilled, multi-shift teams in a fast-paced setting.
• Excellent written and verbal communication skills with the ability to influence and collaborate.
• Experience managing budgets, performance metrics, and operational improvements.
• Proficiency in Microsoft Office applications; SAP experience is a plus.
• Strong decision-making skills with the ability to work independently and respond to changing situations.
• Working knowledge or experience in a Print Department (preferred).
• About Lonza
• Ready to shape the future of life sciences?

Benefits

Additional Information

Job Title Associate Director, Specialty Products Printing Location Greenwood, South Carolina, United States. This role leads a multi-shift manufacturing operation focused on printing and finishing two-piece hard capsules, offering the opportunity to drive quality, productivity, and continuous improvement in a fast-paced pharmaceutical environment. Fully Site-Based Role This is a fully site‑based role. Working together in person supports close, real‑time collaboration and the technical precision needed to manufacture medicines to the highest quality and safety standards. What you will get: An agile career and dynamic working culture. An inclusive and ethical workplace. Compensation programs that recognize high performance. Medical, dental and vision insurance.

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