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The Salesforce Data Integrity Specialist ensures data accuracy and consistency within the Salesforce platform, implements data quality standards, conducts audits, manages user permissions, provides training, and improves data management processes. They collaborate with teams to streamline operations and enhance data accuracy.

The CQV Engineer develops documentation to support Commissioning, Qualifications, and Validation in pharmaceutical facilities. Responsibilities include protocol writing, field verification, and summary report development. Requires 4-8 years of experience in commissioning and qualification activities in FDA regulated industries. Should have experience in facilities and equipment startup, utilities, building automation, and pharmaceutical manufacturing processes.

The Senior CSV Engineer is responsible for validating and qualifying computer systems in compliance with regulatory standards. This includes preparing and reviewing validation documentation, managing change controls, analyzing testing results, troubleshooting issues, coordinating between departments, and participating in regulatory audits.

We are looking for a Junior CSV Engineer with 1-3 years of experience, ideally with at least one year of experience in GMP (Good Manufacturing Practices).

The CSV Engineer will develop and execute protocols and test scripts, consult on resolutions, and write documentation related to GxP computer validation and 21 CFR Part 11. Requires collaboration with industry experts to ensure compliance in the biotech and pharmaceutical sectors.

As a CQV Engineer, you will develop documentation for Commissioning, Qualification, and Validation in pharmaceutical environments, manage protocol writing and execution, and perform field verifications. You'll also provide cGMP guidance for CQV services integration and manage the documentation lifecycle. Strong technical problem-solving skills are essential for troubleshooting and project management.

The CQV Engineer will develop documentation for Commissioning, Qualification, and Validation of pharmaceutical facilities and equipment. Key responsibilities include protocol writing and execution, field verification, and summarizing reports at client sites. The role requires strong problem-solving skills and experience in FDA regulated industries.