Quality and Regulatory Affairs Specialist

Quality and Regulatory Affairs Specialist

At Majeton,weare driven by our commitment to deliver “The Right Product for Health”. Our team of researchers and clinical experts utilize clinic feedback from practitioners, scientifically researched literature and top quality manufacturing as the foundation for all products.

We are seeking a meticulous and experienced Quality & Regulatory Affairs Specialist to join our team and ensure regulatory compliance, uphold product quality, and oversee vigilance reporting for all of our marketed products.

What you will do

Quality Assurance (QA)

• Handle and manage local annual GDPMDS and GDP inspection; support inspection readiness
• Maintain and manage all controls of documents and records
• Manage and maintain local GDPMDS and GDP SOP and system records, including but not limited to all product complaints, returns, disposal, internal inspection / audit, deviation, CAPA management, etc
• Manage new and existing supplier management activities
• Perform personnel training to ensure regulatory and quality compliance

Regulatory Affairs & Pharmacovigilance (RA & PV)

You are someone who

It’s a bonus if you also have

What we offer

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