CQV Analyst

Há 18 horas


Região Geográfica Intermediária de São Paulo São Paulo Brazil PharmEng Technology Tempo inteiro

Join to apply for the CQV Analyst role at PharmEng Technology.

PharmEng Technology, 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
  1. Develop and execute commissioning, qualification, and validation protocols for new and existing equipment and processes.
  2. Conduct risk assessments and gap analyses to identify areas for improvement in compliance and quality.
  3. Perform equipment and process qualifications, including installation, operational, and performance qualifications.
  4. Review and approve validation documentation, including protocols, reports, and deviations.
  5. Collaborate with cross-functional teams, including engineering, manufacturing, and quality, to ensure compliance with regulatory requirements and company standards.
  6. Troubleshoot equipment and process issues and provide technical support to resolve them.
  7. Participate in audits and inspections, both internal and external, and assist with implementing corrective and preventative actions.
  8. Keep up-to-date with industry regulations and guidelines related to commissioning, qualification, and validation.
Qualifications
  1. Bachelor's degree in Engineering, Pharmacy, Chemistry, or a related field.
  2. Fluent in English and Portuguese.
  3. Minimum of 3 years experience in commissioning, qualification, and validation in the pharmaceutical industry.
  4. Strong knowledge of FDA and cGMP regulations.
  5. Experience with equipment and process validation, including IQ/OQ/PQ, cleaning validation, and process validation.
  6. Excellent problem-solving and analytical skills.
  7. Strong attention to detail and ability to work independently.
  8. Excellent communication and interpersonal skills.
  9. Ability to prioritize and manage multiple projects simultaneously.

We offer a competitive salary, along with opportunities for professional growth and development. If you are a self-motivated, detail-oriented individual passionate about ensuring quality and compliance in the pharmaceutical industry, we encourage you to apply for this exciting opportunity. Join PharmEng Technology and make a difference in the lives of patients worldwide.

Additional Information
  • Seniority level: Mid-Senior level
  • Employment type: Full-time
  • Job function: Business Development and Sales
  • Industries: Pharmaceutical Manufacturing
#J-18808-Ljbffr
  • CQV Analyst

    1 semana atrás


    Região Geográfica Intermediária de São Paulo, Brasil PharmEng Technology Tempo inteiro

    Join to apply for the CQV Analyst role at PharmEng Technology . PharmEng Technology, 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...

  • Cqv Analyst

    1 semana atrás


    São Paulo, São Paulo, Brasil PharmEng Nordic ApS Tempo inteiro

    Position: CQV AnalystPharmEng Technology an Efor Group of Companiesis 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...

  • CQV Analyst

    4 semanas atrás


    São Paulo, São Paulo, Brasil PharmEng Nordic ApS Tempo inteiro

    Position: CQV AnalystPharmEng Technology an Efor Group of Companiesis 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...

  • CQV Analyst

    Há 3 dias


    São Paulo, São Paulo, Brasil PharmEng Nordic ApS Tempo inteiro

    Position: CQV Analyst PharmEng Technology an Efor Group of Companiesis 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...


  • São Paulo, São Paulo, Brasil beBeeCqv Tempo inteiro R$60.000 - R$120.000

    CQV Analyst Job SummaryWe are 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.


  • São Paulo, São Paulo, Brasil beBeeCqvAnalyst Tempo inteiro R$60.000 - R$80.000

    CQV Analyst PositionPharmaceutical companies seek highly motivated CQV Analysts to develop and execute commissioning, qualification, and validation protocols for new and existing equipment and processes.Main Responsibilities:Develop and implement commissioning, qualification, and validation strategies to ensure compliance with regulatory requirements.Conduct...

  • Equipment Specialist

    Há 23 horas


    São Paulo, São Paulo, Brasil beBeeValidation Tempo inteiro R$100.000 - R$150.000

    Commissioning, Qualification, and Validation AnalystThe Commissioning, Qualification, and Validation (CQV) Analyst is responsible for ensuring the compliance of equipment and processes within a regulated environment.Develop and execute commissioning, qualification, and validation protocols for new and existing equipment and processes.Conduct risk assessments...