Vaga de parceiro

Quality Analyst - São Paulo / SP

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Detalhes da Vaga

  • Escolaridade Não Informado
  • Segmento Não Informado
  • Salário Não Informado
  • Área de AtuaçãoDiversos / Outros

O que você irá fazer

  • With a mission to empower healthcare professionals to deliver exceptional patient care, CONMED is dedicated to innovation, quality, and excellence in all aspects of our operations.
  • Role reports to: Quality Systems Manager Travel: 10% Job Description Responsible for ensuring, maintaining, and supporting the Conmed Brazil quality management system, complying with regulatory standards and meeting quality, health, and safety standards.
  • Constantly interacts with other areas such as Regulatory Affairs, Sales, Marketing, and Supply Chain, from Brazil and from other countries.
  • Responsible for ensuring the quality of existing products and processes, ensuring that changes are documented and do not negatively impact product performance and quality.
  • This is an excellent opportunity for growing in an international medical device company.
  • The responsibilities will include: Ensure compliance with ConMed Policy, Quality Standards, and regulatory requirements.
  • Contribute to the development and review of SOPs, work instructions, and other quality documentation as needed.
  • Maintain accurate and up-to-date records of all QMS activities in accordance with regulatory requirements (RDC 665/22) and ConMed procedures.
  • Support investigations of non-conformances and deviations and contribute to the implementation of corrective and preventive actions.
  • Document and analyze QA data, trends, and deviations to identify opportunities for process improvement and optimization.
  • Support training programs on quality issues to ConMed team members and suppliers.
  • Support training activities to customers related to product complaint process.
  • Support the daily operations of ConMed branches.
  • Communicate with suppliers and warehouses to address and implement quality-related processes and policies.
  • Position Requirements: Bachelors degree in pharmacy/biosciences or equivalent field.
  • Previous experience in quality assurance, preferably within the medical device industry.
  • Familiarity with relevant regulatory requirements and quality standards (e.
  • g.
  • , ISO 13485, ANVISA RDC 665/22).
  • Quick problem-solving and analytical skills with attention to detail.
  • Strong collaboration skills and the ability to work independently.
  • Strong knowledge of Brazilian regulatory standards (e.
  • g.
  • , Anvisa).
  • GMP Auditor RDC 665/22.

Informações Adicionais

  • Quantidade de Vagas 1
  • Jornada Não Informado
 

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