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The Quality Control Specialist III role involves executing Molecular Bioassay techniques, analyzing data for Biologic Products, troubleshooting instrumentation, leading investigations, and supporting quality control functions. The position requires technical leadership in analytical method validation and coordination of continuous improvement efforts in a laboratory setting.

The Senior Manager, Quality for Combination Products at Gilead is responsible for managing compliance and ensuring that the Quality Management System (QMS) meets global regulations for combination products. This role involves monitoring industry standards, participating in audits and inspections, engaging with various stakeholders, and leading improvements in QMS processes to support the development and market advancement of combination products.

The Senior Research Associate I will support small and large-molecule drug discovery by planning and conducting protein production experiments, performing protein expression and purification, troubleshooting challenges, and communicating results with project teams.

The Manager of Quality Systems is responsible for enhancing and integrating Quality Systems, documenting QA projects, managing stakeholder relationships, and ensuring project performance and risk management throughout the project lifecycle. The role includes guiding junior staff and staying updated on industry trends to improve QA processes.

The Senior Research Associate II will play a key role in drug discovery for Virology, Oncology, and Inflammation by engineering, expressing, purifying, and characterizing proteins. They will handle protein quality assessments using biophysical analytics and collaborate with cross-functional teams to present results.

The Quality Assurance Operations Specialist II interacts with contract manufacturers to resolve quality issues and ensures compliance with regulatory requirements. They participate in developing SOPs, maintain quality programs, review production documents, and lead investigations related to quality control. This role requires strong knowledge of quality systems and an ability to work independently and collaboratively within teams.

The Sr. Manager, Biostatistics will lead biostatistical analysis for clinical studies, provide statistical consultation, and support NDA submissions. Responsibilities include overseeing statistical activities, participating in clinical development planning, and contributing to trial design discussions.