Job Description:

The Supervisor Packaging will play a part in the facility start-up, with primary responsibilities focused on supporting daily manufacturing operations and the timely production of pharmaceuticals at the Civica Petersburg, VA site. In collaboration with stakeholders, this position will lead day-to-day Packaging Operations, running all packaging equipment, supporting new product introductions on the packaging lines, equipment qualifications, change management, investigations, training, and development. The ideal candidate will have a consistent track record of achieving results in a fast-paced Pharmaceutical Packaging environment.

Essential Duties and Responsibilities: Essential Duties and Responsibilities

• Lead the Packaging team to execute daily and weekly production schedules to meet operations objectives.

• Conduct daily shift meetings to communicate current events, issues, and solicit team feedback.

• Monitor Packaging team productivity and resolve immediate production needs to facilitate efficiency. Coordinate the team’s break and lunch periods to minimize production downtime.

• Manage daily and weekly staffing requirements to account for absent personnel (PTO) to satisfy production needs. Coordinate overtime scheduling as needed.

• Monitor the inventory of packaging supplies. Report any quality issues and shortages to prevent production interruptions.

• Conduct training and ensure staff training is documented, is current, and follows cGMP requirements.

• Review batch records, cycle reports, and other manufacturing documentation to identify and address any potential quality issues.

• Perform and/or oversee batch accountability calculations and final batch quantity confirmations.

• Provide immediate support in the identification and documentation of deviations and discrepancies on the packaging floor.

• Support cross-departmental activities including maintenance, qualification, testing, and investigational activities.

• Assist in the development and update of manufacturing procedures and training materials.

• Perform other duties as assigned by manufacturing management.

• Assist R&D and MSAT on new product introduction and tech transfer activities to meet commercial demand.

• Initiate and complete manufacturing investigations including root cause analysis and product impact assessment.

• Assist in the creation, revision, and management of manufacturing documents such as Batch Records and SOPs.

Basic Qualifications and Capabilities: Basic Qualifications (Knowledge, skills, and abilities)

• 8+ years’ experience in a GMP manufacturing environment. Packaging Operations experience preferred.

• 2 years’ supervisory experience in a GMP manufacturing environment with associate degree, or equivalent experience and knowledge.

• Strong writing and documentation skills.

• Experience in a process improvement environment, including change management, optimizing process flow, and participating in Lean/Six Sigma project teams.

• Proficiency in Microsoft Office applications.

Physical Demands and Work Environment:

The physical demands described here are representative of those required to perform the essential functions of this position. Reasonable accommodation may be provided to enable individuals with disabilities to perform the functions. While performing the essential duties of this position, the employee is regularly required to speak or hear. The employee is frequently required to use their hands or fingers, handle or feel objects, tools, or controls. The employee is occasionally required to stand, walk, sit, and reach with hands and arms. The employee must occasionally lift and/or move up to 40 pounds. The noise level in the work environment is usually low to moderate. The company is an Equal Opportunity Employer, a drug-free workplace, and complies with ADA regulations as applicable.