CQV Analyst

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 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. 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, 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

Location: Região Geográfica Intermediária de São Paulo, São Paulo, BR

Posted Date: 11/3/2025