Senior Quality Assurance Specialist

FujifilmMadison, WI

About The Position

Support Quality Assurance initiatives, ensure implementation of Quality Management Systems and compliance with applicable regulations, guidelines, and quality standards. This role provides interacts with cross functional teams providing support for the manufacture of products. This role performs a range of tasks which include but are not limited investigations, document creation, metric generation and ensure compliance of the quality system. Orchestrate, track and maintain essential documentation (SOPs, manufacturing records, specifications, change controls, third party records) as they progress through, and eventually reside in, the document control system. Regularly apply Innovation, initiative, and attention to detail to identify deficiencies and improve the efficiency of information flow through this system.

Requirements

  • Bachelor’s degree in a life science discipline such as but not limited to cell biology, biochemistry, or microbiology, or its equivalent
  • 5 years of relevant quality assurance experience with demonstrated achievements and progressive responsibilities.
  • Demonstrated organizational; problem solving; decision-making; communication (oral and written); and influencing skills – dealing with diverse stakeholders
  • Detailed focused, with demonstrated writing and communication skills using MS Office.
  • Functional knowledge of cGMP principles and practices.
  • Functional proficiency with an electronic Quality Management System
  • Able to work at computer for extended periods

Responsibilities

  • Review of documents and records used to support Good Manufacturing Practice and Discovery Research Operations, approving quality assurance records as appropriate, ensuring compliance with current SOPs
  • Coordinate the review and revision of Documents within the eQMS system.
  • Assist with preparation, formatting, distribution, routing, and maintenance of SOPs and other version-controlled documents.
  • Create and maintain system for document storage and maintenance.
  • Manage the company’s training record storage system.
  • Conduct new hire orientation training and development activities for the QMS system.
  • Oversee maintenance of quality system processes to ensure compliance with regulatory and business objectives.
  • Support or lead investigations, root cause analysis by making data driven and technical decisions, using critical thinking skills.
  • Write, revise, and review standard operating procedures and operational documents (eg. Manufacturing procedures and Quality Control procedures).
  • Provide quality assurance support to organization.
  • Ensure compliance with all applicable domestic and international regulatory requirements and quality system regulations and standards associated with product manufacture and release.
  • Generate quality metrics as needed.
  • Other job functions as assigned.
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