̽»¨ºÏ¼¯

̽»¨ºÏ¼¯ is seeking a CQV Engineer to join a team, focusing on GMP warehouse operations. This role requires immediate availability and is based entirely in Stein. The successful candidate will play a crucial role in ensuring compliance and quality within the warehouse environment.

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:

• Oversee commissioning, qualification, and validation (CQV) activities for the GMP warehouse.
• Ensure all processes meet regulatory and quality standards.
• Collaborate with cross-functional teams to implement and maintain warehouse systems.
• Identify and resolve any issues related to warehouse operations.
• Document and report on CQV activities and outcomes.

Key Skills and Requirements:

• Proficiency in English at C1 level; German language skills are advantageous.
• Strong understanding of GMP regulations and warehouse operations.
• Excellent problem-solving and communication skills.
• Ability to work independently and manage multiple tasks effectively.

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.

̽»¨ºÏ¼¯ is a leading life sciences recruiter focused on finding exceptional people and matching them with the finest positions across the globe. ̽»¨ºÏ¼¯ is acting as an Employment Agency in relation to this vacancy.