Regulatory & Compliance

•      Ensure all food supplement products comply with requirements 

•      Manage labelling review, health claim substantiation, and product notifications in line with UK and EU frameworks.

•     Manage and handle registration of products

 

2.  Medical Affairs & Pharmacovigilance
  

•      Serve as the internal scientific reference point for technical queries from distributors, customers, and regulatory bodies.

•      Prepare medico-scientific materials including training content, Product presentation and sientific/marketing contents.

 

3.  Product Development & Formulation
•      Evaluate new product concepts for scientific feasibility and regulatory viability prior to launch commitment.

•      Review and approve product specifications, certificates of analysis (CoAs), and stability data from manufacturing partners.

•      Coordinate with contract manufacturers and testing laboratories throughout the product lifecycle.

 

4.  Supplier Technical Liaison


•      Review supplier technical documentation (CoAs, stability reports, ingredient dossiers) and support qualification activities.

•      Provide technical input during partnership negotiations and distribution agreement evaluations.

 

5.  Quality Assurance & GMP/GDP Oversight

•      Maintain a quality management system (QMS) appropriate to the company's supplement operations and regulatory environment.

•      Ensure GMP and GDP principles are applied across sourcing, handling, and distribution of supplement products.

•      Prepare and control SOPs, quality agreements, and technical documentation; support any regulatory inspections or partner audits.