Job Description


Position: CQV Analyst

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, ...

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