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Visual Inspection Program Leader

Fresenius Kabi USA

Wilson, NCOnsitePosted 31 days ago$73,614 - $103,528
Full TimeSenior LevelQuality (QA / QC)Pharmaceutical
Original posting ↗

Summary

The Visual Inspector Program Leader is responsible to Lead the design, development, and implementation of visual inspection standards for parenteral products, ensuring compliance with regulatory requirements, industry best practices and FK local and global SOP's. Acts as high-level knowledge in automated and manual visual inspection. Collaborates with local and global teams for all Visual Inspection initiatives including Knapp studies, Defect level tracking, and visual inspection control strategy. Responsible for training and qualifying operators.

Job description

Job Summary

The Visual Inspector Program Leader is responsible to Lead the design, development, and implementation of visual inspection standards for parenteral products, ensuring compliance with regulatory requirements, industry best practices and FK local and global SOP's. Acts as high-level knowledge in automated and manual visual inspection. Collaborates with local and global teams for all Visual Inspection initiatives including Knapp studies, Defect level tracking, and visual inspection control strategy. Responsible for training and qualifying operators.

Responsibilities

Visual Inspection Program Development

  • Lead the design, development, and implementation of visual inspection standards for parenteral products, ensuring compliance with regulatory requirements and industry best practices.
  • Evaluate and validate visual inspection processes, including both manual and automated inspection methods, to achieve optimal quality outcomes.
  • Establish risk-based inspection strategies for different types of parenteral products and materials (e.g., vials, syringes).
  • Harmonize visual inspection control strategies and practices across the internal and external manufacturing network.
  • Manage Defect kit implementation process.
  • Manage Defect catalogue and Library in collaboration with MQA.

Technical Expertise & Process Optimization

  • Serve as the high-level knowledge on visual inspection processes, equipment, and quality standards for the parenteral product line.
  • Conduct root cause analyses and implement corrective and preventive actions (CAPAs) for quality related events.
  • Collaborate with cross-functional teams (QA, manufacturing, engineering, TSMS) to identify and implement process improvements that enhance efficiency and reduce inspection errors.

Training & Development

  • Develop and deliver training programs for quality inspectors, operators, and other relevant staff, focusing on the visual inspection of parenteral products and adherence to GMP requirements.
  • Mentor junior staff and develop training materials to promote inspection skills and quality awareness within the organization.

Compliance & Documentation

  • Ensure compliance with FDA and any other global applicable regulatory standards by keeping inspection processes and documentation up-to-date and audit-ready.
  • Participate in internal and external audits, providing expert insights and support for any inspection-related findings.
  • Act as high level knowledge for the development and maintenance of internal quality system documents (Global Q standards, Common Q practices) and execution documents (validation reports, PoDs) to support the visual inspection Quality System.

Innovation & Continuous Improvement

  • Explore and evaluate new technologies and methodologies in visual inspection, including AI, to enhance accuracy and efficiency.
  • Identify opportunities for process automation, working closely with engineering teams to implement new tools and technologies.

Requirements

  • High-level expertise in manual and automated visual inspection processes for parenteral products
  • Capable of leading cross-functional teams
  • Maintaining audit-ready documentation in accordance with global quality standards

Benefits

  • 401(k) Matching
  • Paid Vacation
  • Holiday & Personal Days
  • Employee Assistance Program
  • Medical, Dental & Vision
  • Life Insurance
  • Disability Insurance
  • Wellness Program

Company overview

Fresenius Kabi USA is a leading global healthcare company and a subsidiary of Fresenius Kabi AG, specializing in pharmaceutical manufacturing and medical technologies. Headquartered in Lake Zurich, Illinois, the company operates as a comprehensive provider of essential medicines and technologies for critically and chronically ill patients. With over 43,000 employees globally and a presence in more than 100 countries, Fresenius Kabi USA focuses on four complementary business areas: Biopharma (biosimilars for autoimmune diseases and oncology), Pharma (IV drugs and infusion therapy), Medical Nutrition, and MedTech. The company's extensive portfolio includes injectable drugs, delivery systems, advanced transfusion medicine, cell therapy technologies, clinical nutrition products, and infusion devices. Serving hospitals, long-term care facilities, alternate care sites, and clinics, Fresenius Kabi USA is committed to providing high-quality, lifesaving medicines and technologies while driving healthcare transformation through innovation and patient-centric solutions.

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