Packaging Supervisor - 2nd Shift, Lead & Improve Quality

NCBiotech; Raleigh (NC); On-site; USD 65,000 - 95,000; Full time

Job summary

Guerbet in North Carolina is seeking a Packaging Supervisor for the 2nd shift to oversee pharmaceutical packaging operations, ensuring cGMP compliance.

The role requires 3+ years of supervisory packaging experience, strong communication skills, and the ability to train and mentor staff. You will drive process improvements, support CAPA and change control, coordinate validations, and participate in safety and regulatory activities.

Qualifications

• Minimum 3 years of supervisory experience in a packaging environment.
• Excellent verbal and written communication skills.
• Ability to present information to large groups.
• Good interpersonal skills.
• Willingness to work flexible hours.
• BS Degree in Life Sciences or Engineering.
• Six-Sigma Greenbelt or Lean Certified.
• SAP Transaction Management.
• Mechanical aptitude.

Responsibilities

• Supervise packaging operations to meet production schedules.
• Oversee packaging of pharmaceutical products ensuring quality and regulatory compliance.
• Prepare and review packaging process documentation.
• Train and mentor personnel on packaging processes.
• Identify and implement packaging process improvements (CAPA).
• Coordinate validation activities for packaging processes.
• Write Deviations related to packaging operations.
• Support change control initiatives.
• Oversee related engineering studies.
• Performs other duties as assigned.

Skills

Supervisory packaging

Communication skills

Present to groups

Interpersonal skills

Flexibility

Education

BS Degree in Life Sciences or Engineering

Six-Sigma Greenbelt

Tools

SAP Transaction Management

Job description

Guerbet in North Carolina is seeking a Packaging Supervisor for the 2nd shift to oversee pharmaceutical packaging operations, ensuring cGMP compliance.

The role requires 3+ years of supervisory packaging experience, strong communication skills, and the ability to train and mentor staff. You will drive process improvements, support CAPA and change control, coordinate validations, and participate in safety and regulatory activities.