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ÌìÑÄÉçÇø¹ÙÍø is seeking a dedicated QA Expert Senior to join the Quality Assurance team. This role focuses on ensuring compliance and quality oversight during the manufacturing and release process of bulk drug substances. You will play a key role in maintaining high standards of quality and regulatory compliance.

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 compliance and quality during the manufacturing and release process of bulk drug substances.
• Represent the QA department in routine GMP activities and improvement projects.
• Ensure accurate reporting within various systems and documentation in line with current guidelines and regulatory requirements.
• Participate in GMP zone audits and internal/external regulatory inspections.
• Promote continuous improvement initiatives.
• Understand and apply EHS guidelines, ensuring personal safety and reporting risks or improvement opportunities.
• Act as a backup for other QA Experts and QA Manager/Supervisor as needed.

Key Skills and Requirements:

• Strong understanding of GMP and regulatory compliance.
• Experience in quality assurance within a manufacturing environment.
• Ability to participate in audits and inspections.
• Commitment to continuous improvement and safety standards.
• Excellent communication and documentation skills.

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.

ÌìÑÄÉçÇø¹ÙÍø is a leading life sciences recruiter focused on finding exceptional people and matching them with the finest positions across the globe. ÌìÑÄÉçÇø¹ÙÍø is acting as an Employment Agency in relation to this vacancy.