Vaga de parceiro

Cqv 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

  • 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 validationQualifications:- 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 simultaneouslyWe 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 PharmEng Technology and make a difference in the lives of patients worldwide.
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Informações Adicionais

  • Quantidade de Vagas 1
  • Jornada Não Informado
 

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