Lead Packaging & Labeling Supervisor (GMP)

Run my Accounts AG; Frederick (MD); On-site; USD 85,000 - 110,000; Full time

Job summary

SriSai Biopharmaceutical Solutions (SBS) seeks a Packaging & Labeling Supervisor to lead daily operations in a regulated biopharma environment.

You will supervise packaging/ labeling activities, ensure batch records accuracy, and maintain readiness for audits while mentoring a team.

The role requires hands-on leadership, strict compliance with cGMP and FDA labeling rules, and a focus on continuous improvement.

Qualifications

• Bachelor’s degree in Life Sciences, Operations Management, or a related field.
• 3–5 years of packaging, labeling, or GMP-regulated operations experience.
• Previous supervisory or team leadership experience.
• Strong knowledge of cGMP, GDP, FDA labeling requirements, and documentation practices.
• Familiarity with label reconciliation, batch tracking systems, and ERP software.
• Exposure to Lean, 5S, or continuous improvement methodologies.

Responsibilities

• Supervise daily packaging and labeling activities to ensure compliance with batch records, SOPs, and labeling controls.
• Verify products are packaged and labeled accurately according to cGMP and FDA requirements.
• Review and approve line clearances, equipment logs, and documentation.
• Lead training and development of Packaging & Labeling staff.
• Collaborate with QA to resolve deviations and CAPA activities.
• Maintain accurate cGMP documentation and support audits.

Skills

cGMP knowledge

GDP knowledge

FDA labeling

Documentation

Lean/5S

Team leadership

ERP software

Batch tracking

Education

Bachelor’s degree in Life Sciences / Operations Management

Tools

ERP software

Batch tracking systems

Job description

SriSai Biopharmaceutical Solutions (SBS) seeks a Packaging & Labeling Supervisor to lead daily operations in a regulated biopharma environment.

You will supervise packaging/ labeling activities, ensure batch records accuracy, and maintain readiness for audits while mentoring a team.

The role requires hands-on leadership, strict compliance with cGMP and FDA labeling rules, and a focus on continuous improvement.