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The Oncology Medical Writer (Senior Manager/Associate Director) leads the development of regulatory documents related to clinical studies, ensuring compliance with internal and external standards. Responsibilities include managing document processes, collaborating with project teams, identifying information gaps, maintaining timelines, and proposing process improvements. The role requires effective communication and problem-solving skills to drive decision-making and document production.
The Senior Manager/Associate Director of Medical Writing creates and manages complex documents for clinical studies and regulatory interactions, leading project teams and collaborating with subject matter experts. Key responsibilities include document development, project timeline management, and strategic alignment with departmental goals. This role requires strong organizational skills and the ability to communicate effectively across teams.
In this role, the incumbent supports the Vendor, Reagent, and Sample Logistics operations within Pfizer's Vaccine Research and Development. Responsibilities include sample management, document handling, compliance with GxP regulations, equipment maintenance, and lab inventory management, all while working in a team setting to maintain operational efficiency.
As a Senior Associate I - Regulatory Change Manager, you will ensure compliance with regulatory standards, manage submissions to regulators, provide training, oversee systems coordination, and contribute to project completion. Your role is vital in meeting operational goals and facilitating communication between teams to resolve complex issues.
The Medical Quality Governance Manager is responsible for leading local medical quality initiatives, ensuring compliance, and enabling audit readiness. This role involves collaborating with stakeholders to manage quality events, implementing strategic initiatives, and analyzing performance to promote a culture of quality in assigned markets.
This role involves designing and developing digital solutions for cash management projects, managing timelines and resources, creating user-centric experiences, and overseeing project completion according to SDLC guidelines. The Associate will also document processes and train stakeholders.
Lead the technical support for manufacturing applications and core platforms while overseeing technology and vendor partnerships. Drive efficiencies in manufacturing operations using DevOps practices and adopt agile frameworks to ensure production aligns with company requirements. Foster a culture of automation and continuous improvement.
The Senior Director, Global Supply Engineering & Sustainment will lead technical support for manufacturing applications, oversee vendor partnerships, design DevOps practices, and ensure architecture governance to boost efficiency in Pfizer's manufacturing operations.
The Senior Director of Global Supply Engineering & Sustainment will lead the technical support for manufacturing applications, enhance operational efficiency through DevOps practices, implement agile methodologies, and ensure architecture governance while managing technology partnerships at Pfizer.
The Senior Director of Global Supply Engineering & Sustainment at Pfizer will lead the technical support for manufacturing applications, oversee technology and vendor partnerships, and ensure architecture governance. This role focuses on driving efficiencies and sustainability in manufacturing operations through DevOps practices and adherence to agile frameworks while fostering a collaborative work environment.
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