Caro usuário, habilite o javascript para que esse site funcione corretamente.

CQV Analyst

CLT (Efetivo)Presencial (Local)São Paulo-SPEmpresa Confidencial (Cadastre-se)

* Salário: R$ 2.000 a R$ 5.000 por mês (estimado)

* O valor exibido é uma estimativa calculada com base em dados públicos e referências do mercado. Não garantimos que este seja o salário oferecido para esta vaga específica.

Área: Outros

Nível: Junior

Position: CQV Analyst

Confidencial (Apenas para Cadastrados) an Efor Group of Companies is seeking a highly motivated and experienced CQV Analyst to join our team. This is a full time, permanent position with opportunities for growth and development within our company. As a CQV Analyst, you will be responsible for ensuring the quality and compliance of our pharmaceutical manufacturing processes and equipment.

Key Responsibilities:

  • Develop and execute commissioning, qualification, and validation protocols for new and existing equipment and processes
  • Conduct risk assessments and gap analyses to identify areas for improvement in compliance and quality
  • Perform equipment and process qualifications, including installation, operational, and performance qualifications
  • Review and approve validation documentation, including protocols, reports, and deviations
  • Collaborate with cross-functional teams, including engineering, manufacturing, and quality, to ensure compliance with regulatory requirements and company standards
  • Troubleshoot equipment and process issues and provide technical support to resolve them
  • Participate in audits and inspections, both internal and external, and assist with implementing corrective and preventative actions
  • Keep up-to-date with industry regulations and guidelines related to commissioning, qualification, and validation

Qualifications:

  • Bachelor's degree in Engineering, Pharmacy, Chemistry, or a related field
  • Fluent in English and Portuguese are a must
  • Minimum of 3 years experience in commissioning, qualification, and validation in the pharmaceutical industry
  • Strong knowledge of FDA and cGMP regulations
  • Experience with equipment and process validation, including IQ/OQ/PQ, cleaning validation, and process validation
  • Excellent problem-solving and analytical skills
  • Strong attention to detail and ability to work independently
  • Excellent communication and interpersonal skills
  • Ability to prioritize and manage multiple projects simultaneously

We offer a competitive salary, as well as opportunities for professional growth and development. If you are a self-motivated and detail-oriented individual with a passion for ensuring quality and compliance in the pharmaceutical industry, we encourage you to apply for this exciting opportunity. Join our team at Confidencial (Apenas para Cadastrados) and make a difference in the lives of patients worldwide.