Quality Regulatory Consultant

Mantell Associates is partnered with a global biopharmaceutical organisation based in León, specialising in the development, manufacturing, and commercialisation of biosimilars, alongside offering integrated CDMO services worldwide.

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With continued investment driving growth, they are looking to expand their Quality Control team with an experienced QC Consultant. This is a fully onsite role within a GMP-regulated laboratory environment.

QC Consultant - Responsibilities:

• Perform analytical testing in line with GMP requirements
• Support stability studies and routine QC testing
• Prepare and manage reagents, solutions, and laboratory materials
• Ensure accurate and compliant documentation of all laboratory activities

What's on offer:

• Opportunity to join a high-growth, investment-backed CDMO
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• Work on advanced biopharmaceutical products
• Collaborative and fast-paced environment
• Competitive daily rate

Mantell Associates is a specialist Pharmaceutical and Life Science headhunting firm. For more information on this opportunity, contact us at