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The Senior Corporate Counsel will provide legal advice to clinical, medical, and regulatory teams in the pharmaceutical industry with a focus on Rare Disease or Diabetes. Responsibilities include developing legal strategies, ensuring compliance, communicating with colleagues, and presenting innovative legal solutions for complex issues.
The QMS Partner will ensure compliance with GMP standards by maintaining the Quality Management System, preparing for inspections, and leading quality improvement initiatives. Responsibilities include managing quality trends, training new employees, and collaborating across departments to enhance quality operations. The role requires excellent communication skills and the ability to manage multiple projects effectively.
The Director of Research Data Governance will develop and execute a cohesive data governance strategy, ensuring compliance with regulations such as GDPR and HIPAA. Responsibilities include managing the data lifecycle, overseeing data quality, building a governance team, and reporting on initiatives to senior management.
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The Senior/Principal Scientist will lead drug discovery initiatives in chronic kidney disease, working with a multidisciplinary team to identify new treatment options. Responsibilities include scientific leadership, managing projects using advanced translational tools, evaluating external opportunities, and representing the organization at conferences.
As a Trial Manager, you'll oversee and manage clinical trial activities to ensure timely delivery, maintaining quality and productivity. Responsibilities include project management, providing clinical input for trial design, coordinating team communications, and supporting the conduct and closure of trials while sharing best practices for process improvement.
As a Category Manager, you will develop and execute category strategies for sourcing Single Use Systems and Components while managing supplier relations, conducting negotiations, and aligning contracts with corporate guidelines. You'll collaborate with suppliers and stakeholders to optimize supply chain processes and contribute to continuous improvement efforts.
The Global SIMA Manager is responsible for overseeing global operations, ensuring operational excellence, managing a 24/7 shift schedule, and leading problem and change management processes. The role involves stakeholder engagement, agile collaboration with the Product Owner, and delivering quality communications within the team.
The Supply Chain Project Manager is responsible for managing high-complexity projects in supply chain coordination with Contract Manufacturing Organizations (CMOs). Key tasks include developing supply chain processes, establishing communication channels, and facilitating timely delivery of test materials while collaborating with various departments and stakeholders.
The Health & Safety Partner will lead EHS integration projects, ensuring procedures are onboarded across Novo Nordisk's factories. Responsibilities include coordinating the EHS Portal implementation, managing health and safety initiatives, and preparing sites for ISO45001 re-certification.
The Vice President & Head of Staffs P&O Business Partnering will lead the development and execution of HR strategies at Novo Nordisk, focusing on finance, legal, global solutions, and corporate development. This role involves acting as an advisor to the CFO, overseeing a team, and collaborating on diverse HR matters such as talent management and organizational effectiveness.
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