Job Description

Packaging Line Supervisor—Glen Rock, PA

Responsibilities:

• Supervise and coordinate daily operations of the primary and secondary pharmaceutical packaging lines.
• Ensure all packaging activities are conducted in full compliance with GMP, SOPs, and regulatory requirements (FDA, EU, etc.).
• Oversee serialization and aggregation activities in accordance with DSCSA and global compliance standards.
• Lead and mentor a team of packaging technicians and operators, providing training, performance feedback, and development opportunities.
• Monitor line performance and troubleshoot operational issues to minimize downtime and improve productivity.
• Collaborate with Quality Assurance (QA), Quality Control (QC), and Engineering to ensure timely batch release and resolution of deviations.
• Perform and document line clearance, in-process checks, and reconciliation activities in accordance with batch records and SOPs.
• Review and ensure accuracy of batch documentation, logbooks, and serialization records.
• Maintain proper inventory and staging of packaging components and materials.
• Drive continuous improvement initiatives related to safety, quality, and efficiency.
• Effectively communicates and interacts with other associates and customers.
• Participates in problem-solving efforts.
• Conducts all work activities in a safe, responsible and professional manner consistent with all Company Policies, Quality Systems Requirements and Relevant Regulatory Standards (e.g. 21CFR211).
• Drives deviation investigations; develops and implements preventative actions.
• Participates in training and supports the designs for equipment trainings.
• Ensures all packaging SOPs are up to date and makes revisions when required.
• Performs other duties and responsibilities as assigned.

Job Requirements:

• Associate or Bachelor’s degree in Life Sciences, Engineering, or a related field preferred. Equivalent experience considered.
• Minimum 3–5 years of experience in a supervisory or lead role within a pharmaceutical packaging environment.
• Strong working knowledge of cGMP regulations and industry best practices.
• Hands-on experience with serialization and aggregation systems (e.g., Antares, Systech, SEA Vision, or similar).
• Proven ability to lead, motivate, and manage packaging teams in a fast-paced, regulated setting.
• Excellent organizational, problem-solving, and communication skills.
• Ability to work various shifts as needed and maintain flexibility in a dynamic production environment

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