Jobs and Careers
CA

Senior Specialist II - Quality Assurance

Catalent Pharma Solutions
United Statesfull_timeVerifiedPosted 27 Apr 2026

About the role

Senior Specialist II - Quality Assurance

Position Summary:

  • Work Schedule: M-F 8am-5pm
  • 100% on-site

Working for Catalent Biologics is an opportunity to join an entrepreneurial team.  Catalent Biologics is making significant investments in people and capabilities.  This is a unique opening to join a small, fast-growing business, backed by a global public company.  People joining our team will have the opportunity for career development as our business continues to grow and expand.  Catalent-Madison employees are helping to improve future patient outcomes by working on products that are designed to treat COVID-19, cancer, various autoimmune, fibrotic and blood disorders, HIV, diabetes, heart and lung diseases as well as Alzheimer’s.

Catalent Pharma Solutions in Madison, WI is hiring a Senior Specialist II - Quality Assurance.

The Quality Assurance Operations group has oversight of the manufacturing areas, including process technology transfer, master batch record review and approval, on-the-floor support, product disposition, and shipping.

The Role:

  • Responsible for maintaining and enhancing the effectiveness of the Quality System through ensuring
    compliant preparation and execution of production.
  • Responsible for representing Quality Assurance as the primary contact for assigned projects, which
    includes cross functional internal and external collaboration, supporting integration of the client programs
    into the Catalent Quality Management System and ensuring effective management of client expectations.
  • Responsible for interfacing with the clients and managing internal communication to sustain and enhance
    the Client quality relationships,
  • Accountable for review and approval of project related documents such as Master Batch Production
    Records, technical transfer, and process characterization reports.
  • Accountable for review and approval of project related deviation investigation records.
  • Accountable for ensuring that Finished Products are manufactured and tested in a manner consistent with
    the applicable regulatory or client requirements.
  • Responsible for final approval and disposition of finished product for shipment to customers.
  • Maintains a high level of understanding of the quality systems and operations to provide consultation and
    guidance for Manufacturing personnel regarding execution of the Quality Management Systems.
  • Develops and provides training to support the training program for QA and manufacturing on specific
    quality functions.
  • Supports and enhances effectiveness of the quality system, including reporting metrics; developing,
    authoring and approving Standard Operating Procedures (SOPs); identifying improvement opportunities;
    implementing change control, risk management, and corrective and preventive action processes.
  • Drives alignment and improvement initiatives, leading cross functional teams to address process
    improvement, system improvement, and new regulations / expectations.
  • Acts as the quality contact and Subject Matter Expert (SME) for Quality Assurance operations and
    Quality management of client programs.
  • Provide program specific review of documents supporting process validation and regulatory filings.
  • Lead continuous improvement projects for the Quality Assurance Operations department.
  • Notifies Management of potential quality or regulatory issues that may affect product quality or
    regulatory compliance.
  • Performs and supports any other tasks necessary to maintain the product quality and site CGMP
    compliance.
  • All other duties as assigned
     

The Candidate:

  • Doctorate Degree in STEM discipline with minimum of 2 years related experience.
    OR
  •  Master's Degree in STEM discipline with minimum of 5 years related experience.
    OR
  • Bachelor's Degree in STEM discipline with minimum of 7 years related experience.
  • Ability to use Excel, Word, and other office systems.
  • Prior work experience with quality management software such as TrackWise® or ComplianceWire®.
  • Ability to independently apply GMPs to everyday work.
  • Maintains data

Apply for this role

Generate a tailored application kit with a matched cover letter, interview prep, and CV highlights — in under 60 seconds.

Apply Now →Generate Application Kit

Free account required — sign up in 30s

Company

Catalent Pharma Solutions

View company profile →