Quality Assurance Manufacturing Specialist

Are you passionate about quality and precision? Join our client with this QA Manufacturing role and help ensure top-tier standards every day.

R&D Partners is seeking a dedicated QA Manufacturing Specialist to ensure quality standards are upheld during the production of pharmaceutical products. In this role, you will be a key player on the manufacturing floor, ensuring compliance with Good Manufacturing Practices (GMP) and supporting the production of safe and effective medicines.

Responsibilities:

• Oversee manufacturing processes in real time to ensure they meet quality standards.
• Monitor and document production steps, including cleaning, material handling, and equipment setup.
• Identify and report any issues or deviations during production and assist in resolving them.
• Review and verify production records for accuracy and compliance.
• Support environmental monitoring and ensure proper cleanroom practices.
• Conduct routine checks and participate in audits to maintain GMP compliance.
• Provide training and guidance to production teams on quality and documentation practices.
• Assist in investigations and corrective actions related to quality findings.

Key Skills and Requirements:

• Strong understanding of quality assurance in a regulated manufacturing environment.
• Knowledge of GMP and aseptic processes.
• Effective communication and coaching skills to guide teams.
• Ability to handle deviations and make decisions in a fast-paced environment.
• Collaborative mindset with a focus on maintaining product integrity and compliance.

For more information, please contact Henry LeLacheur.

If you are interested in applying to this exciting opportunity, then please click ‘Apply’ or to speak to one of our specialists visit the ‘Contact Us’ page.

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

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