Processor, Formulations I

Responsibilities

• Blend and process formulation ingredients according to defined specifications to produce high-quality master batches.
• Monitor production processes using statistical controls, inspection systems and product sampling to maintain quality and compliance.
• Identify and promptly address process deviations to ensure safe, efficient and controlled operations.
• Supply formulation materials to manufacturing equipment in alignment with production schedules and downstream requirements.
• Maintain accurate production documentation in accordance with Good Manufacturing Practices (GMP).
• Maintain clean, organized and safe work areas that support product quality and regulatory compliance.
• Support team success by providing backup coverage for other Formulations Processors and contributing to safety, quality, attendance and productivity goals.

Requirements

• High school diploma or GED equivalent.
• Ability to perform calculations involving percentages, decimals and fractions.
• Experience using or the ability to learn precision weighing and measurement equipment.
• Basic computer skills and the ability to accurately maintain production records.
• Ability to lift, push and pull materials weighing up to 50 lbs.
• Ability to achieve a score of 50 or less on the Color Hue Test.
• Ability to work a 12-hour night shift schedule, including weekends, holidays and additional hours as business needs require.
• About Lonza
• Ready to shape the future of life sciences?

Benefits

Additional Information

Job Title Processor, Formulations I - 12hr Night Shift (7:00 PM- 7:00 AM) Location Greenwood, South Carolina, USA Join Lonza's Formulations team in Greenwood, SC, where you will play a critical role in producing high-quality formulation materials that support the hard capsule manufacturing process. This is an exciting opportunity to contribute to a fast-paced production environment while developing expertise in manufacturing operations, quality, and process control. 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. Opportunities for growth within a global life sciences organization. A collaborative team environment focused on safety, quality and continuous improvement.

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