Product development

Nutris; Madrid; Presencial; EUR 30.000 - 45.000; Jornada completa

Descripción de la vacante

A leading company in the Food and Pharmaceutical Industries seeks a Quality Assurance professional. The role involves managing technical documentation, ensuring regulatory compliance, and supporting customers. Ideal candidates will hold a Bachelor's in Health Science and have 3-5 years experience in the industry.

Formación

• 3-5 years experience in Quality Assurance or Regulatory Affairs in Food Supplements or Food Industry.
• Deep knowledge of European Food Regulation (EFSA).
• Fluent in English (C1 level) both written and spoken.

Responsabilidades

• Manage and follow-up on technical documentation needs of customers and suppliers.
• Support in developing the Quality Management System (BRC / IFS / GMP standards).
• Provide technical support to customers and manage customer claims.

Conocimientos

Analytical skills

Data management

Communication

Regulatory compliance

Educación

Bachelor's Degree in Health Science

Herramientas

Microsoft Office

Business management systems (ERP)

Descripción del empleo

Nutris is a highly motivated company, whose steps are based on a constant innovating activity and following the most exigent quality procedures in both Food and Pharmaceutical Industries. Nutris team works with the commitment to offer the most innovative and qualified products to our customers. Our clinically proven and patented products constitute the main proof of our innovation engagement.

Qualification and Experience Requirements :

A combination of education and work experience skills is preferred :

• Bachelor's Degree in Health Science (Food Science, Pharmacy, Biology, Biotechnology, Chemistry or related field).
• Demonstrate relevant working experience from three (3) to five (5) years in Quality Assurance and / or Regulatory Affairs in Food Supplement Industry (preferable) or Food Industry.
• Deep knowledge of European (EFSA) Food Regulation, preferably applied to Food Supplements. Knowledge of FDA regulations are also valuable.

Language :

• Fluent English (minimum C1), written and spoken, able to provide response to technical queries.
• French knowledge will be positively valued.

Informatics :

• Microsoft office (user level), including Outlook.
• Used to work with databases and business management systems (ERP).

Personal Skills and Abilities :

• Ability to assess compliance and deal with international regulations and organisms (EC, EFSA, etc.).
• Strong analytical and data management skills.
• Great communication skills, both spoken and written, inside the organization and with external companies. Communication with customers.
• Proactive, decided, organized, methodical and with strong teamworking abilities.

Job Expectations :

Joining the Technical Department, focused on finished products business line, you will be developing the following functions :

• Maintenance of documental database with the required information, as per the internal protocols.
• Customer technical support.
• Management and follow-up of technical documental needs of customers and suppliers.
• Management of customer claims, ensuring compliance with domestic and international regulations.
• Approvement of new and existing specifications in compliance with regulatory requirements for the intended use and targeted markets.
• Support at developing the Quality Management System (based on BRC / IFS / GMP standards).
• Coordination with QA Director to perform monitoring metrics for tracking the compliance and process effectiveness.