QA Support Expert

Project overview

QA Support Expert

Reference: 572b0665-5d6e-4737-ab63-adea39f7cfd0

• A growing pharmaceutical company

Responsibilities

• Review and release of deviation reports and CAPAs in the GMP environment (aseptic manufacturing)
• Follow-up of necessary corrections
• Ensuring the implementation of customer comments
• Assessment of the technical and qualitative plausibility as well as the risk adequacy of deviations
• Support of the QA team in deviation management (incl. tracking & trending)
• Coordination with internal stakeholders and customers

Requirements

My advantages:

• Sound knowledge in the area of Quality Operations
• Experience with cleanroom class D environments and handling aseptic & sterile conditions
• Familiarity with the requirements of FDA and GMP standards
• Fluent German & English
• A demanding project with the option for extension

Project details

asap

3 months

• Start: ab sofort
• Duration: 3 Monate
• Remote: onsite
• Location: Nordrhein-Westfalen, Deutschland, DE
• Languages: German

Source notes

With over 15 years of experience in the classic pharmaceutical industry, biotechnology, chemistry, and medical technology, we know the key contacts who advertise demanding tasks with potential. The high demand for personnel opens up exciting opportunities for dedicated specialists and managers to develop professionally and work on their own careers. As a specialized personnel consultancy with an international network, we offer you decisive advantages – and all this free of charge for you. Register and benefit from interesting and suitable positions and projects.

My contact at Hays:

My contact person:

Maria Shadrina

Reference number:

*

Contact:

Email: *@*.de