Pharma Labeling Project Coordinator & Tech Services

Lonza Inc. in; Tampa (FL); On-site; USD 65,000 - 85,000; Full time

Benefits offered by this job

Medical, dental, and vision insurance

Career development opportunities

Cross-functional collaboration

Job summary

Lonza in Tampa, FL is seeking a Project Coordinator – Technical Services Specialist to support labeling and packaging operations in a highly regulated pharmaceutical environment. You will coordinate label design, proofs, approvals, and production to keep projects on schedule while interfacing with clients and internal teams.

The role requires an associate degree in a related field (or equivalent experience), strong attention to detail, and proficiency with Microsoft Office.

Qualifications

• Associate degree in Project Management, Life Sciences, or related field; equivalent experience considered.
• Experience in pharmaceutical/regulated manufacturing environment.
• Knowledge of label design, printing, document control, or packaging operations.
• Strong proofreading skills with high attention to detail.
• Ability to manage multiple priorities in a fast-paced setting.
• Experience with Microsoft Office applications (Word, Excel, PowerPoint, Visio).
• Effective communication and collaboration across teams.

Responsibilities

• Coordinate label design, proofs, approvals, and production to support packaging timelines.
• Interface with clients and internal teams to relay project updates and resolve issues.
• Manage label production schedules, inventory, and documentation to avoid delays.
• Ensure labeling processes comply with cGMP, quality standards, and regulatory expectations.

Skills

Labeling operations

Cross-functional collaboration

Attention to detail

Multitasking

Communication skills

Education

Associate degree in Project Management

Tools

Microsoft Word

Microsoft Excel

PowerPoint

Visio

Job description

Lonza in Tampa, FL is seeking a Project Coordinator – Technical Services Specialist to support labeling and packaging operations in a highly regulated pharmaceutical environment. You will coordinate label design, proofs, approvals, and production to keep projects on schedule while interfacing with clients and internal teams.

The role requires an associate degree in a related field (or equivalent experience), strong attention to detail, and proficiency with Microsoft Office.