Specialist Quality Assurance Qualification & Validation (f/m/d)


Offered by:

Bavarian Nordic Berna GmbH


Your responsibilities: Responsible, as QA representative in multidisciplinary teams, to oversee and review/approve qualification/validation documents and risk assessments for the following topics:Qualification of Equipment, Facilities, UtilitiesComputer System Validation (CSV)In this role the QA Specialist:

  • leads the implementation of the qualification/validation strategy
  • supports the transfer from project into commercial production phase
  • is the QA representative during qualification/validation work
  • ensures that the allocated quality-systems are compliant with regulatory expectations
  • establishes and continuously improves quality procedures within the area of responsibility
  • continuously improves the allocated quality systems
  • supports changes and corrections for the area of responsibility
  • participates in audits and inspection within the area of responsibility

 What you bring to the table:

  • Master’s degree in Engineering, Biotechnology, or related field.
  • Minimum of 5 years relevant experience in a GxP regulated pharmaceutical/biotechnology industry.
  • Minimum of 3 years validation and qualification experience required
  • Solid computer skills including MS Office required.
  • Analytical thinking and problem-solving attitude
  • Multilingual – at least German and English, written and spoken

 We provide an opportunity to be a part of an international company that boasts exceptional technology and a determined team. Join our dedicated and agile IT team if you share our enthusiasm and have a desire to create an impact. You can expect a vibrant and adaptable work environment that supports the growth of your personal and academic skills. Additionally, we offer an extensive benefits package and a competitive compensation package. Caught your interest?We look forward to receiving your application directly on our recruiting portal: