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American Regent

Produces sterile injectable medications for healthcare

Inspection and Packaging Supervisor

Machine & Process OperationPosted on Nov 9
Full-timeNew Albany, OH, USANo salary listedIn-person

About the Job

Requirements

  • A high school diploma or GED is required.
  • Experience with current good manufacturing practice guidelines and FDA regulations is required.
  • Experience with an HMI-PLC/SCADA control data system in a relevant field is required.
  • One to three years of experience in a leadership role in the inspection and packaging area is required.
  • Applicants must have good oral and written English communication and comprehension skills.
  • Applicants must be able to perform basic mathematical calculations.
  • Applicants must be able to take feedback constructively and function in a team-oriented work environment.
  • Applicants must be able to work overtime as needed.
  • Applicants must be physically able to wear laboratory protective gowning and equipment, including gowns, goggles, face shields, respirators, and protective gloves.
  • Applicants must be able to occasionally lift and/or move up to 50 pounds.

Responsibilities

  • Ensure equipment and supply inventories are maintained and available for use according to production schedules.
  • Ensure only approved materials and equipment are used.
  • Ensure personnel do not perform tasks without accurate and approved training records.
  • Ensure only approved documentation and procedures are used.
  • Coordinate scheduling activities with the Filling Department to ensure timely product processing.
  • Analyze department performance and implement strategies to improve employee safety, product quality, and productivity.
  • Identify and address individual and team training and development needs.
  • Staff inspection and packaging operating stations to support the production schedule.
  • Ensure proper QC sampling techniques and procedures are used and samples are delivered to the QC laboratory on time.
  • Analyze staffing needs and make appropriate staffing adjustments.
  • Ensure GMP-compliant operations are performed by the Inspection and Packaging Team.
  • Attend training programs required by company SOPs, procedures, and policies.
  • Develop operational tactics for manufacturing startup activities.
  • Prepare for pre-approval inspections and prepare for and participate in regulatory audits.
  • Ensure workplace safety and security across manufacturing areas in accordance with OSHA, EPA, DEA, and other applicable governing-body standards.
  • Interview, hire, and train employees; plan, assign, and direct work; appraise performance; reward and discipline employees; and address complaints and resolve problems.
  • Oversee and provide signatory approval for activities associated with inspection and packaging, including inspection, labeling, packaging, cartoning, cleaning, assembling, and QC sample collection.
  • Direct, train, and mentor inspection and packaging staff as needed.
  • Ensure proper operation of inspection, labeling, and packaging equipment and that processes remain compliant and inspection-ready.
  • Ensure proper use of batch documentation.
  • Troubleshoot manufacturing processes and equipment, making adjustments and minor repairs during setup and operations as needed.
  • Provide input and assistance in creating inspection and packaging batch records.
  • Participate in inspection and packaging activities, including automated inspection, labeling, and packaging; manual glass-vial inspection; and equipment teardown and line clearances.

Desired Qualifications

  • A bachelor's degree in Pharmaceutical Science, Chemistry, Biology, Engineering, or a related field is preferred.
  • Experience with fully automated inspection and packaging systems is preferred.

About the Company

American Regent

Produces sterile injectable medications for healthcare

American Regent is a pharmaceutical company that develops, manufactures, and supplies sterile injectable medicines for U.S. and Canadian healthcare providers, including brands and generic injectables. Its products are produced in sterile form and used by hospitals, clinics, and other providers to treat patients. The company operates manufacturing sites in New York, Ohio, and Pennsylvania and ships across the United States and Canada, aiming to ensure a steady, broad portfolio of injectable therapies for patients. It differentiates itself through its commitment to reliable supply and through ongoing investments to modernize and expand its U.S. manufacturing capabilities, supporting sustainable growth and the well-being of its employees and customers. Its goal is to maintain a steady supply of high-quality injectable medicines by expanding capacity and improving efficiency to serve the healthcare marketplace.

Company size
501-1,000
Company stage
Not listed
Total funding
Not listed
Headquarters
New York, NY
Founded
Not listed

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