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The Process Engineer will design and specify cGMP process equipment, manage small-to-medium scale projects, participate in design reviews, and support QA Validation. Responsibilities also include revising diagrams, investigating control system issues, implementing process improvements, and ensuring compliance with relevant laws.

As an Inside Sales Specialist at CAI, you'll drive revenue growth in the life sciences by identifying and closing new business opportunities, collaborating with sales and marketing teams, and managing the sales process from lead generation to closing. Responsibilities include cold calling, utilizing Salesforce, managing sales activities, and developing a deep understanding of products and services to communicate value to customers.

The Quality Specialist at CAI will ensure compliance with quality systems and regulatory requirements, perform batch record reviews, and facilitate adherence to GMP standards. This role involves improving quality systems, supporting commercial manufacturing quality, and collaborating with clients to solve complex problems.

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).

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.

As a Project (CQV) Engineer, you will perform commissioning, qualification, and validation activities in a safety-focused environment. Your responsibilities include generating procedures, reviewing equipment design, preparing qualification reports, managing timelines, coordinating with contractors, and ensuring efficient project execution.

The CSV Engineer will develop and execute validation protocols/documents, manage change controls, participate in audits, troubleshoot issues, assess compliance of systems, and coordinate with departments or contractors to maintain regulatory adherence in computer validation processes.