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Azenta

Automated cold-chain sample management and multiomics

Quality Assurance Associate

Validation, Compliance & Quality SystemsConfirmed live in the last 24 hours
Full-timeWotton, Dorking, UKNo salary listedIn-person

About the Job

Requirements

  • A Bachelor's or Associate Degree in Education, Life Science, Science, Chemistry, Business, Engineering, or a related field.
  • Two years of experience in quality assurance or a related field.
  • Working knowledge of Change Control and Document Control.
  • Understanding of how nonconforming outputs are resolved using the 8D corrective action methodology (Eight Disciplines).
  • Ability to understand complex documents related to life sciences and medical device design and manufacture, including Quality Manuals, Design History Files, Device Master Records, Device History Records, Post Market Surveillance, Instructions For Use, and Periodic Safety Update Reports.
  • Organizational and small project management skills, including the ability to manage multiple projects and meet deadlines.
  • Proficiency with the Windows platform and Microsoft Office programs including Microsoft Teams, Excel, and Visio; familiarity with related applications such as Planner, Microsoft To Do, Tasks, or equivalents.
  • Ability to facilitate successful presentations and training programs for individuals and large groups at all levels of the organization.

Responsibilities

  • Maintain and improve the Quality Management System at multiple manufacturing sites in accordance with FDA Quality System Regulation.
  • Oversee internal audits, host customer audits, and assist the Quality Manager with certification body audits to ensure compliance with ISO 9001 and ISO 13485 standards.
  • Act as gatekeeper for the document control process at the Wotton site.
  • Ensure training on new and updated processes is completed on time.
  • Create and progress document-related change controls as needed.
  • Conduct regular internal audits at both manufacturing locations.
  • Evaluate processes, procedures, and documentation for compliance with quality standards.
  • Identify areas for improvement and recommend corrective actions.
  • Host customer audits as required.
  • Coordinate with cross-functional teams to provide necessary information and address audit findings.
  • Maintain positive relationships with customers during the audit process.
  • Prepare for and participate in certification body audits.
  • Ensure compliance with ISO 9001 and ISO 13485 requirements.
  • Collaborate with relevant departments to address non-conformities.
  • Assist the Quality Assurance team with monitoring quality indicators and trends.
  • Report findings to senior leadership.
  • Identify training needs and deficiencies related to quality.
  • Communicate with senior leadership, colleagues, and global teams.
  • Collaborate with Engineering, Manufacturing, and other departments to maintain quality standards.

Desired Qualifications

  • Internal Auditor experience is preferred.

About the Company

Azenta

Automated cold-chain sample management and multiomics

Azenta provides life sciences solutions focused on end-to-end sample management and genomic services. It combines automated ultra-cold storage, cryogenics, consumables, instruments, and repository services with genomic services like sequencing and gene synthesis through its GENEWIZ brand. The company offers an integrated stack of hardware, consumables, software (LIMS like Limfinity and Freezer Pro), and services to collect, store, and analyze biological samples across their lifecycle. Its end-to-end portfolio and recurring revenue, supported by acquisitions, differentiate it from competitors and aim to speed up drug development, clinical research, and advanced cell therapies by preserving sample integrity from collection to analysis.

Company size
1,001-5,000
Company stage
IPO
Headquarters
Burlington, MA
Founded
1978

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