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American Regent

Produces sterile injectable medications for healthcare

QC Environmental Monitoring Supervisor

Regulatory & Quality (Life Sciences)Posted on Nov 11
Full-timeHilliard, OH, USANo salary listedIn-person

About the Job

Requirements

  • A high school diploma or GED equivalent is required.
  • Two to three years of experience in a pharmaceutical aseptic processing environment, production quality assurance, aseptic testing, the medical device or food industry in microbiology, or a combination of these areas is required.
  • Previous experience in environmental monitoring or sampling, writing environmental monitoring protocols and investigations, water sampling, performing qualification of new environmental monitoring and water systems, and gown qualification programs is required.
  • Experience with instruments such as Met One, APC, Air Ideal, MAS 100, MAS 100 CG, Lighthouse System, or PMS system is required.
  • The employee must be flexible with working hours, dependable, and able to work overtime as needed according to the production schedule.
  • The employee must be able to work responsibly and accountably within a multidisciplinary team environment.
  • The employee must have excellent computer skills and proficiency in Microsoft Word, Excel, and Outlook.
  • The employee must be able to wear cleanroom and protective gowning and equipment, including goggles, face shields, respirators, and protective gloves.
  • The employee must have 20/40 near vision, correctable with eyeglasses or contacts, and color vision.
  • The employee must maintain a clean-shaven appearance each working shift to wear tight-fitting respirators properly.
  • The employee must be able to occasionally lift and/or move up to 25 pounds.

Responsibilities

  • Supervise the environmental monitoring program and technicians under the direction of the Microbiology Manager.
  • Complete and maintain gown qualification and gown training for other staff members at Hilliard.
  • Provide technical and administrative support for environmental monitoring activities and documentation.
  • Coordinate work projects with the Microbiology Manager and schedule environmental monitoring workload to meet department and site requirements.
  • Schedule employees according to workload to improve efficiency.
  • Assist environmental monitoring technicians with sampling and other environmental monitoring responsibilities as required.
  • Review standard operating procedures as necessary, recommend changes, and update and initiate change controls as needed.
  • Review environmental monitoring paperwork for accuracy and completeness and submit it to the laboratory with plates for timely incubation.
  • Issue and perform internal investigations, deviations, or event reports, and ensure timely closure of reports for nonconforming results.
  • Perform and maintain environmental monitoring data tracking and trending, and present reports to the Microbiology Manager.
  • Ensure and check inventory of media and materials required for the environmental monitoring program, and order supplies as necessary.
  • Interact closely with and support manufacturing and quality personnel in environmental monitoring.
  • Assist the Manager with timely completion of quarterly and other periodic projects and reports.
  • Perform other tasks and duties assigned by management.

Desired Qualifications

  • A bachelor's degree in microbiology, biology, environmental sciences, or a related scientific field is preferred.
  • One to two years of lead or supervisory experience is preferred.
  • The employee should be able to mentor subordinates.
  • The employee should have excellent verbal and written communication skills.
  • The employee should be adaptable and maintain flexibility in a changing and challenging environment.
  • The employee should demonstrate ownership and take responsibility.

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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