À±½·ÊÓƵ

À±½·ÊÓƵ is seeking a dedicated Quality Control Associate to ensure operations align with cGMP regulations. This role involves supporting quality metrics and analysis and requires collaboration across various departments. The ideal candidate will have a proactive approach to identifying discrepancies and experience in GxP manufacturing is beneficial.

Please note that to be considered for this role you must have the right to work in this location or hold an EU passport.

Responsibilities:

• Ensure all operations comply with cGMP regulations.
• Support the identification and resolution of discrepancies.
• Collaborate with cross-functional teams within the quality line organization.
• Contribute to quality metrics and analysis.

Key Skills and Requirements:

• Proficiency in English (minimum B1 level); German language skills are advantageous.
• Basic knowledge of Microbiology and Chemistry.
• Experience in buffer and solution preparation.
• Initial experience in aseptic techniques.
• Strong organizational skills and ability to work independently.
• Effective communication skills with management, peers, and external partners.
• Familiarity with productivity software (Word, Excel, Outlook).
• Knowledge of LabWare LIMS and Oracle systems is a plus.

If you are having difficulty in applying or if you have any questions, please contact Ashley Bennett at a.bennett@proclinical.com.

Apply Now:

If you are interested in learning more or applying to this exciting opportunity, please complete the form below and attach a copy of your CV. Alternatively, for further details or to talk directly to a life sciences recruitment specialist, please request a call back at the top of this page.

À±½·ÊÓƵ is a leading life sciences recruiter focused on finding exceptional people and matching them with the finest positions across the globe. À±½·ÊÓƵ is acting as an Employment Agency in relation to this vacancy.