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COMPLIANCE & QUALITY ASSURANCE MANAGER - MEDICAL CANNABIS

Descrição da oferta de emprego

9 months project with the possibility of joining permanently the company Vendas Novas & Lisboa Sobre o nosso cliente Medical Cannabis Company focused on the cultivation, processing, extraction and research and development.
Descrição Design, adapt and implement the company's QMS; Develop, write, maintain, administer, train, and manage quality systems documents that can be used effectively and meet Infarmed and ISO quality system requirements; Build an internal training program to ensure quality awareness and regulatory compliance knowledge across the company; Responsible for and lead in all aspects of the company's compliance, in particular risk management, SDLC and design control; Provide counsel, training, coaching and interpretation of quality assurance requirements and Infarmed and other regulatory guidelines or issues to company personnel; Act as a liaison between the company and regulatory authorities; Ensure the proper interface of the CQA function to cultivation, product development, commercialization, manufacturing, supply chain, and other areas as required; Plan and prepare document packages for submission to global regulatory agencies; Foster a strong relationship, partnership and advocacy with Infarmed and Global Health authorities, as it relates to innovation in cannabis.
Monitor proposed and current relevant EU regulations and guidance and advise; Provide Quality Assurance leadership for Good Manufacturing Practices (GMP) product quality systems and activities; Support and guide throughout the project, ensuring high quality expectations are met and technical readiness requirements are met in all phases of development.
Perfil ideal Master's degree with a focus in Life Sciences or equivalent; Experience in QA within the Pharmaceutical / Medical cannabis industry; Experience developing, improving and maintaining Infarmed and ISO compliant quality management systems; Knowledge and experience with external standards.
ISO , ISO , IEC , ISO and 21 CFR 820 (FDA cGMP/QSR), especially pertaining to product development, manufacturing, supplier management, quality control and customer complaints; Expert knowledge in advanced CQA systems, including the establishment of relevant CQA metrics; Entrepreneurial, innovative, energetic, hands-on, team oriented, and customer focused, with the ability to think strategically as well as execute project details.
Vantagens Opportunity to join a young, dynamic and forward-looking company set to disrupt the medical cannabis space in Europe.
Project of 9 months with the possibility of joining permanently the company.
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Detalhes da oferta

Empresa
  • Michael Page Portugal
Localidade
  • Em todo Portugal
Endereço
  • Indeterminado - Indeterminado
Tipo de Contrato
  • Indeterminado
Data de publicação
  • 01/11/2024
Data de expiração
  • 30/01/2025
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