Manufacturing Quality and Technical Manager

Quincy Bioscience (QB), a biotechnology company located in Madison, WI is searching for a Manufacturing Quality and Technical Manager to work in either our Plano, TX or Madison, WI facilities. This role is responsible for ensuring compliance with Good Manufacturing Practices in all work performed related to the manufacture of food ingredients and dietary supplement products.

  • Responsible for performing audits of warehousing, contract manufacturing vendors and internal quality control activities. Ensures compliance to in-house specifications, standards, and good manufacturing practices.
  • Assists with auditing and qualifying CMOs.
  • Monitors and maintains vendor compliance to specifications and standards for quality and food safety.
  • Assists with technology transfer.
  • Assists with communicating with CMOs and investigating quality performance issues.
  • Responsible for developing, applying, revising, and maintaining quality standards for processing materials into partially finished or finished products. Designs and implements methods and procedures for inspecting, testing, and evaluating the precision and accuracy of products and prepares documentation for inspection testing procedures.
  • Assist with designing and conducting training programs.
  • Assists in all customer and regulatory inspections and responses.
  • • Assist with optimization and maintenance of systems for performing, tracking, and trending of Investigations, Deviations, and Corrective Actions.
  • Develops and maintains applicable Quality and Manufacturing metrics and communicates critical metric information to management.
  • Provides support to the company on issues of product and ingredient performance. Assists in investigation and resolution of quality incidents from all internal and external customers. Assists in providing regulatory support to retail and manufacturing operations.
  • Assists in writing and maintaining food, ingredient, and packaging specifications.
  • • Ensures quality systems are compliant with all current GMP and FSMA requirements.
  • Performs review of manufacturing and analytical documentation for accuracy and compliance with GMP.
  • Write and revise Standard Operating Procedures (SOPs).
  • Support product development and current product manufacturing activities.
  • Maintains leadership role through active participation in leadership team meetings, presentations to site staff on Manufacturing, Quality/Compliance and Technical issues.

The ideal candidate for this role is reliable, hardworking, and high energy.

Ideal candidates will have a bachelor’s degree in a scientific discipline or equivalent. A minimum of 6 years in a regulated food, dietary supplement or pharmaceutical setting preferred, as is ASQ certification. Excellent oral and written communication and interpersonal skills are required.

In turn we offer a competitive wage and robust benefits package.

If this describes you and you are interesting in contributing to a successful, growing organization, please submit your resume and cover letter to for consideration.

Quincy Bioscience – The Makers of Prevagen
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