Top Tech Jobs & Startup Jobs

The Process Characterization and Technology Scientist will support the Downstream Investigations Team focusing on raw materials. Responsibilities include troubleshooting processes, leading lab studies on manufacturing processes, analyzing data, and preparing technical documents. The role involves working in a biotech lab environment to enhance process knowledge and support medicine production.

The Supervisor, Document Control position involves managing a team responsible for maintaining and revising documentation systems, preparing reports for management, ensuring compliance, training staff, and coordinating document requests during regulatory inspections. The role emphasizes quality, organization, and leadership.

The Senior Specialist, Global Procurement supports procurement initiatives in Regulatory Affairs & Health Economics by conducting data analysis, assisting in cost savings, and managing vendor sourcing activities. Responsibilities include the RFx process, contract negotiations, and overseeing supplier performance. This role also involves using tools for spend analysis and ensuring compliance with procurement policies.

The Principal Statistical Programmer will lead programming activities for clinical studies, ensuring timely and high-quality deliverables. Responsibilities include programming documentation, regulatory submission support, and collaboration with internal and external teams. Required skills include proficiency in SAS and knowledge of statistical concepts and clinical trial principles.

As a QA Specialist, you will ensure manufacturing documentation aligns with quality standards, participate in investigations and problem resolution, train junior employees, review controlled documents, and represent QA in cross-functional meetings. You'll focus on continuous evaluation of procedures and support technical transfer activities through documentation oversight.

The Senior Statistical Programmer supports study teams by implementing programming standards and maintaining documentation for clinical studies. This role includes providing programming deliverables for study reports, regulatory submissions, and ad hoc analyses while collaborating with cross-functional teams to ensure compliance and traceability in accordance with regulations.

The Administrative Coordinator provides administrative and project support to the Corporate Affairs department, including budget tracking, Purchase Order management, scheduling for the SVP, and event coordination. Key responsibilities also involve vendor onboarding, meeting logistics, and supporting team communication and inquiries.