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, Utilities

Computer 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: https://candidate.hr-manager.net/ApplicationInit.aspx?cid=1576&ProjectId=146796&DepartmentId=18964&SkipAdvertisement=true