Top Software Engineer Jobs

The Regional Coordinator for Material Master Data ensures the safe supply of medicines globally by reviewing material master data submissions, providing training and technical support, managing audit deliverables, developing key performance metrics, and enhancing processes for efficiency. This role requires collaboration with global stakeholders and a focus on continuous improvement initiatives.

As a Senior Quality Assurance Specialist, you will evaluate and review clinical and commercial batches, ensuring compliance with established specifications and processes. Responsibilities include conducting investigations, managing change controls, providing quality oversight, and maintaining compliance with Good Manufacturing Practices. You will contribute to quality review and assist in improving procedures, ensuring that products meet regulatory standards and support the delivery of safe and effective products to patients.

You will manage engineering verification for GMP systems to ensure compliance and quality at Pfizer. This role includes overseeing capital project schedules, documenting system life cycles, and facilitating cross-functional teamwork. Your expertise will support routine reviews and regulatory audits, enhancing project delivery and operational efficiency within a biopharmaceutical environment.

As a Senior Associate in Automation Engineering, you will manage manufacturing information systems to ensure operational efficiency and minimize downtime. Responsibilities include developing project plans, performing maintenance, analyzing process problems, authoring change control, and mentoring junior staff. You will also contribute to cybersecurity alignment and after-hours support for automation systems.

The Process Engineer will monitor and participate in production processes, optimize operations, prepare GMP documentation, and engage in problem-solving for predictive maintenance. Responsibilities include production planning, incident investigation, and cooperation with production support units.

The Senior Scientist will develop and optimize biotherapeutics by modeling protein structures and utilizing AI/ML to enhance property prediction. They will collaborate with project teams and improve computational workflows while analyzing data to enhance drug properties.

The Safety Data Management Specialist will monitor drug, biologics, and medical devices safety programs by evaluating adverse reports, supporting clinical trials, and preparing safety-related documents. Key responsibilities include project management, team mentoring, data analysis, compliance verification, and liaising with partners on safety data collection.