Quality Assurance Manager

3 weken geleden


Leiden, Zuid-Holland, Nederland Eurofins Netherlands BioPharma Product Testing Voltijd
Job Description

The QA Systems Supervisor plays a critical role in the QA Systems team, overseeing the coordination of tasks and ensuring the implementation of global, European, and national procedures. This position involves direct supervision of employees and reporting to the QA Manager.

Key Responsibilities:

  • Ensure continuous improvement of Quality within Eurofins PROXY
  • Manage the Documentation Management System
  • Implement global, European, and national overarching Eurofins procedures and monitor follow-up activities
  • Manage training documentation for all employees
  • Manage changes, supervise correct handling, and advise employees
  • Manage opiates and associated licenses
  • Conduct internal audits
  • Support external audits by customers and governments
  • Supplier qualification

Duties and Responsibilities:

  • Day-to-day management of a team of QA system employees (5 employees)
  • Provide support and guidance to team members to ensure effective performance
  • Divide work, make working agreements, and monitor progress
  • Conduct staff interviews in consultation with the QA Manager
  • Release equipment, facilities, and utilities
  • Optimize QA Systems processes based on Lean principles, considering the interests of other departments
  • Supervise the implementation of GMP regulations and procedures
  • Coordinate back-office during client audits and authority inspections
  • Establish and monitor Quality KPIs related to QA systems
  • Drive quality improvement projects within QA systems
  • Act as backup for the QA Manager for QA Systems-related tasks
Requirements
  • Minimum Bachelor level education in a life science related subject
  • Experience in a GxP environment, preferably pharmaceutical industry, service laboratory, or biotechnology
  • Experience in managing a team, including hire/fire, evaluation, and goal-setting responsibilities
  • Experience in working in a pharmaceutical-, biotechnology-, or service laboratory
  • Knowledge of pharmaceutical quality systems
  • Preferably experience in validation and qualification of equipment, utilities, and facilities
  • Flexible and stress-resistant; able to work effectively in a dynamic environment
  • Responsible, pro-active, and problem-solving mindset
  • Excellent interpersonal skills, flexible, and collaborative
  • Strong team player and leader with the ability to work across multiple functions and disciplines
  • Skill in organization and prioritization, and attention to details
  • Good command of the Dutch and English language, both verbally and in writing
  • In possession of a valid work permit

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