GMP Quality Assurance Associate Consultant

Elevate your career in pharmaceutical consulting as a GMP Quality Assurance Associate Consultant. This position is designed for those passionate about ensuring client project success through compliance.

With a focus on managing quality and compliance projects, you'll engage in tasks ranging from deviation investigations to assisting with Health Canada audits. The role supports various critical projects that ensure the standards of pharmaceuticals, biologics, and medical devices are met. As you refine your skills in either Q&C Services or QCR, you'll significantly enhance client trust in the industry’s best practices.

Key Responsibilities:

• Manage and execute critical compliance projects

• Conduct assessments to close regulatory gaps

• Communicate key project milestones and updates

• Complete tasks involving product release and documentation

• Assist in preparing for audits and inspections

Requirements:

• Bachelor’s degree in Science is essential

• 1 to 3 years of related pharmaceutical experience

• Knowledge of CAPA and deviation processes

• Exposure to audit environments is a plus

• Familiar with product quality reviews and assessments

Bring your expertise in quality assurance and compliance to a role that fosters professional growth in the pharmaceutical industry.
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