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Responsible for automation engineering in pharmaceuticals, focusing on DCS and PLC systems, ensuring quality and compliance in projects.

Verista seeks QA Specialists with 3+ years in pharmaceuticals to ensure compliance with regulatory standards and oversee various QA processes.

We are seeking skilled Project Managers with over 3 years of experience in pharmaceuticals or biotech to lead and deliver projects.

The Process Engineer will support design, scale-up, validation, and operational improvements in pharmaceutical manufacturing, focusing on problem-solving and data evaluation.

The CQV Engineer will author and execute validation documentation, run tests, document results, perform impact assessments, and ensure compliance with GMP in a team setting.

The Business System Specialist will manage LIMS master data, provide end-user support, ensure compliance, and assist in process development for lab data management.

The Controls Engineer will design and install control systems for automation, manage projects, create schematics, develop programs, and support troubleshooting in a life sciences environment.

The CQV Engineer will document, validate, and test equipment and systems, adhering to project schedules while maintaining compliance with regulations.

The Senior Automation Engineer leads automation projects, designs electrical panels, implements control systems, and ensures compliance with regulatory standards in a life sciences context.