Hobson Prior is seeking a QA Associate (Batch Record Reviewer) to support a discipline and/or provide a service individually or within a team. The successful candidate will be responsible for writing and reviewing GMP-relevant deliverables and/or related tools to ensure compliance with cGMP and project quality deliverables. This role also involves the review of manufacturing and analytical batch records for specific departments.

Please note that to be considered for this role you must have the right to work in this location.

Key Responsibilities

• Support a discipline and/or provide a service individually or within a team of associates.
• Write and review GMP-relevant deliverables and/or related tools to ensure compliance with cGMP and project quality deliverables.
• Comply with internal and external guidelines regarding quality and safety.
• Review manufacturing and analytical batch records for specific departments.
• Support paper archiving in specific QA operations.
• Ensure completion of related trainings before performing an assigned task.

Requirements

• Degree in a science discipline.
• Ability to address GMP and logistic related questions with line unit experts.
• Scientific, technical and regulatory knowledge in a specific area.
• Basic knowledge of drug development.
• Detailed knowledge of cGMP, working knowledge of safety and environmental regulations and guidelines.
• Good organizational skills.
• Proficiency in German & English (oral & written).

Apply now

If you are interested in learning more or applying to this exciting opportunity then please click "Apply" and upload a copy of your CV. Alternatively, for further details or to talk directly to a life sciences recruitment specialist directly, please select "Contact me" at the top of this page.

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

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