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À±½·ÊÓƵ is seeking a QC Analyst to join a dedicated team. This role will focus on performing and releasing in-process controls, supporting method validation activities, and maintaining existing infrastructures. The successful candidate will require strong attention to detail and the ability to work with time-critical samples.

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:

• Perform and release in-process controls using techniques such as HPLC, CE, and icIEF in compliance with cGMP guidelines.
• Support method validation activities.
• Maintain existing infrastructures.
• Conduct routine final analyses and stability testing for time-critical samples.
• Test and assess random product samples to ensure they meet pre-defined standards.
• Aggregate test data and document results.

Key Skills and Requirements:

• Experience with HPLC techniques.
• Hands-on lab experience in a GMP environment.
• Completed training in analytical work within the pharmaceutical industry.
• Team player with strong communication skills.
• High level of quality awareness and efficient work habits.
• Good comprehension skills, independent, and reliable.
• Safe handling of potentially hazardous substances.
• Proficient in using a PC and standard software.
• Fluent in English; German is a plus.

If you are having difficulty in applying or if you have any questions, please contact Emile De Beer at e.debeer@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.