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The Cleanroom & HEPA Certification Specialist will manage preventive maintenance and certification activities for Cleanroom environments and equipment, coordinate with vendors for certifications, maintain documentation, analyze data, and ensure compliance with SOPs and quality standards.

The Supervisor of Quality Assurance is responsible for overseeing product and raw material disposition, ensuring compliance with quality assurance policies, and leading investigations and evaluations related to process deviations. This position requires supervising direct reports and engaging in continuous improvement efforts.

Design, implement, and support Data Acquisition and Analysis Systems. Troubleshoot manufacturing deviations and anomalies. Develop engineering design documents and test plans. Support manufacturing, engineering, and validation projects. Author system specifications and execute acceptance tests. Review cyber security vulnerabilities. Create and maintain automation system documentation.

The Senior Workplace Coordinator manages workplace strategy projects, providing support for planning, procurement, and installation of lab equipment and furniture. Responsibilities include coordinating day-to-day activities, maintaining budgets, facilitating communication between departments, and managing vendor relations to ensure efficient project execution with minimal disruption.

As a Senior Automation Engineer, you will design and implement software/hardware improvements, provide technical support for manufacturing and quality control, troubleshoot automation system deviations, and develop necessary documentation for equipment. You will work in a regulated environment to improve biopharmaceutical manufacturing processes.

The Principal Project Manager - Engineering designs and specifies biopharmaceutical process equipment, manages projects related to these systems, prepares engineering documentation, and supports QA/Validation departments. This role includes overseeing installation, supporting investigations, implementing corrective actions, and may require domestic and international travel.

The Innovation Protection Specialist is responsible for managing medical device development portfolios, focusing on innovation protection strategies, due diligence, and legal agreements. They collaborate with internal teams to support medical device R&D, provide metrics on intellectual property matters, and educate colleagues on compliance processes.