Full-Time

Senior Manager of Manufacturing

Updated on 8/1/2026

American Regent

American Regent

501-1,000 employees

Produces sterile injectable medications for healthcare

Compensation Overview

$156k - $185k/yr

Shirley, NY, USA

In Person

Category
Biology & Biotech (1)
Required Skills
Inventory Management
Word/Pages/Docs
Quality Assurance (QA)
Excel/Numbers/Sheets
Microsoft Outlook

Get referred to American Regent

See people who can refer or advise you

Requirements
  • A Bachelor of Arts or Bachelor of Science degree is required.
  • At least 5 years of supervisory experience in a current Good Manufacturing Practice-regulated industry is required.
  • At least 7 years of experience in aseptic manufacturing, pharmaceutical, or medical industry, with progressive experience leading to a management position, is required.
  • Ability to work autonomously, manage time effectively, and deliver results in a timely manner.
  • Strong oral and written communication skills.
  • Strong time management, organizational, and project management skills.
  • Knowledge of Microsoft Word, Excel, Outlook, and PowerPoint.
  • Experience with aseptic manufacturing, isolator technology, and cleanrooms.
Responsibilities
  • Manage and lead day-to-day operations for the commercial aseptic manufacturing of drug and device products across departments such as compounding, equipment and component preparation, sterile filling, inspection, and packaging.
  • Ensure supervisors provide daily process oversight and maintain compliance with company standard operating procedures, data-integrity requirements, Good Manufacturing Practice processes, and department-specific requirements.
  • Drive operational excellence through leadership and technical expertise, supporting the continuous development of people and teams, quality, compliance, safety, customer, and financial goals.
  • Provide leadership and technical guidance for manufacturing personnel to foster a collaborative and innovative operational-excellence culture.
  • Provide leadership, communication, and organizational management for non-exempt and exempt personnel, including process supervisors.
  • Hire, develop, and coach employees to ensure optimal performance by manufacturing personnel.
  • Lead employee feedback, mentoring, technical-acumen, and leadership-development processes.
  • Foster continuous improvement through employee selection, training, and mentoring while focusing on operational efficiency and eliminating non-value-added activities.
  • Support plant-wide strategic plans, programs, and activities.
  • Collaborate with interdepartmental and cross-functional teams and lead change initiatives in a timely and productive manner.
  • Identify, follow up on, and lead opportunities to improve manufacturing processes and practices.
  • Manage and lead daily manufacturing operations across one or more value streams.
  • Ensure compliance with regulatory requirements from the Food and Drug Administration, Occupational Safety and Health Administration, Office of Federal Contract Compliance Programs, Environmental Protection Agency, and other applicable bodies.
  • Adhere to environmental, health, and safety standard operating procedures, equipment policies, and department-specific requirements.
  • Ensure adherence to production schedules and hold supervisors and teams accountable for safety and quality compliance.
  • Ensure appropriate trained resources are available to meet scheduled attainment objectives.
  • Ensure inspection readiness of all manufacturing areas.
  • Participate in internal and external regulatory inspections and ensure successful departmental audits.
  • Interface with customers and regulatory personnel during plant audits and inspections.
  • Ensure on-time completion of investigations, corrective and preventive actions for major and critical deviations, and quality events.
  • Review and approve quality reports, validation protocols, and validation reports.
  • Manage change controls.
  • Comply with the company safety program, health and safety mandates, and Occupational Safety and Health Administration requirements.
  • Ensure accuracy of manufacturing management tools, systems, and documentation, including standard operating procedures and on-the-job training materials.
  • Partner with Manufacturing Engineering and Product Management to troubleshoot process issues and drive projects that improve manufacturing processes.
  • Ensure consistent adherence to personnel-policy administration, including attendance control and disciplinary policy.
  • Ensure timely delivery of products to internal and external customers while meeting product quality, yield, operating-cost, and process-efficiency expectations.
  • Coordinate with other managers and customers to ensure quality commitments are satisfied.
  • Participate in and lead project scheduling and staff meetings and provide updates on departmental activities and project status.
  • Ensure timely escalation of manufacturing issues to management and cross-functional support teams when necessary.
  • Advise senior management on production issues and vulnerabilities and develop improvement and risk-mitigation proposals.
  • Ensure profitability through first-time-right product lots and batch records, labor utilization, acceptable units, finished-good yields, throughput, and Overall Equipment Effectiveness.
  • Increase efficiency and profitability by minimizing production downtime, work-in-process inventory, manufacturing cycle time, and setup time.
  • Optimize resources within assigned areas to meet compliance standards and cost discipline.
  • Manage the manufacture and delivery of drug products to meet internal and external customer expectations.
  • Perform other tasks and duties assigned by management.
Desired Qualifications
  • A Master’s degree is preferred.

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

N/A

Total Funding

N/A

Headquarters

New York

Founded

N/A

Get referred to American Regent

See people who can refer or advise you

Simplify Jobs

Simplify's Take

What believers are saying

  • The 2024 TPX-100 partnership targets knee osteoarthritis, opening a new therapeutic area
  • FDA-approved Vasopressin Injection launched in 2024 addresses vasodilatory shock for hospitals
  • 2024 Amneal partnership accelerates generic injectable launches supporting broader market access

What critics are saying

  • Amphastar's vasopressin price war captures 60% hospital contracts in 9 months with high impact
  • Exela's atropine sulfate 0.3mL vial erodes $12M annual revenue in pediatric emergency kits
  • Somerset's patent challenge blocks $15M Multrys launch in 2027 and forces $3M litigation costs

What makes American Regent unique

  • American Regent leads IV iron therapy with 25 years of dominance in the market
  • The company acquired HBT Labs in 2024 to expand into oncology and complex injectables
  • It operates a $68M modernized New Albany facility increasing sterile injectable production capacity

Help us improve and share your feedback! Did you find this helpful?

Benefits

Health Insurance

Life Insurance

Profit Sharing

Paid Time Off

401(k) Company Match