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American Regent

Produces sterile injectable medications for healthcare

R&D Technical Services Manager

Bioprocess & BiomanufacturingPosted on Nov 13
Full-timeNew Albany, OH, USANo salary listedIn-person

About the Job

Requirements

  • A Master’s degree or Ph.D. in pharmaceutical science, analytical chemistry, chemical engineering, or equivalent is required.
  • At least 7–10 years of relevant pharmaceutical industry experience, including at least 1–2 years in a supervisory management position, is required.
  • A scientific background and solid understanding of process development, scale-up, process analytical technology, and analytical method development and validation principles are required.
  • Experience in analytical sciences, including chromatography and spectroscopic techniques, is advantageous.
  • Excellent oral and written English communication skills are required.
  • Ability to prioritize and perform multiple tasks simultaneously is required.
  • Ability to make decisions independently and with appropriate input is required.
  • Ability to work well in a matrix environment, particularly with QA/QC, Manufacturing Operations, Project Management, and Regulatory Affairs, is required.
  • Flexibility in adapting to multiple therapeutic areas interchangeably is required.
  • Strong computer skills with Word, Excel, PowerPoint, and Outlook are required.
  • Ability to wear laboratory protective gowning and equipment, including gowns, goggles, face shields, respirators, and protective gloves, is required.
  • A clean-shaven appearance each working shift is required to wear tight-fitting respirators properly.

Responsibilities

  • Manage and support process development activities for commercial products and new products under development for technology transfer and launches.
  • Act as a Tech Services Lead or manage the Tech Services team representing designated work cell projects.
  • Manage and provide technical support for day-to-day process-related operations investigations.
  • Author, review, and approve Quality Exception/Deviation reports to satisfy company policies and Quality Assurance requirements.
  • Be responsible and consulted on production and operations process flows to improve efficiency and production yields.
  • Review and/or approve technology transfer reports, process validation reports, supplemental validation reports, manufacturing risk assessments, and other technical reports, as applicable.
  • Approve reporting employees’ timecards and attendance in accordance with company policy.
  • Manage laboratory work to support product or process/technical troubleshooting, special investigations, and product complaints with sufficient supervision.
  • Support FDA deficiency activities and work with Regulatory Affairs on new and existing submissions.
  • Work closely with QA management to facilitate timely internal and external audit responses, especially by facilitating and fulfilling QA’s needs during FDA audits or queries.
  • Set individual goals and conduct performance reviews, manage employee development, recognize employee contributions, mitigate conflict and communication problems, plan and facilitate team activities, select personnel, and motivate members of the functional area.
  • Perform other tasks and duties as assigned by management.

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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