Top Pharmaceutical Jobs

The Clinical Scientist will oversee clinical data monitoring and contribute to regulatory submissions for oncology and hematology programs, collaborating cross-functionally to ensure study execution and quality.

The Psychotherapist provides therapeutic and diagnostic services to patients, conducts intakes, collaborates with care teams, and documents progress accurately.

The Program Manager will manage relationships with major gift donors, optimize fundraising strategies, and oversee the Grateful Patient Program operations.

Join a fellowship-trained Hand and Upper Extremity Surgeon team in Fargo, ND, with call coverage and a collaborative environment.

Supports cross-functional teams in automating systems, analyzing business problems, and assisting in technology evaluations. Involves project participation and consultation for data management.

Senior regulatory leader responsible for global regulatory strategy for Endocrinology programs (rare disease and obesity), leading a team of three, partnering cross-functionally to optimize development, lifecycle management, compliance, and commercial value from early development through post-marketing.

Lead Toxicology/Safety Pharmacology projects, manage studies, advise on findings, prepare regulatory documents, and mentor junior scientists.

The Director of Global Quality GMP Processes leads the optimization of product quality systems, ensuring compliance with GMP and regulatory standards, and oversees global quality metrics and initiatives.

The Neuroscience Specialist will engage healthcare providers using various tools to enhance customer experience, manage outreach, and collaborate on business strategies.

The Associate Director, Biostatistics will provide statistical expertise in drug development, oversee statistical tasks, and collaborate with various teams to support clinical trials.

The QC Scientist will perform QC testing, ensure GMP compliance, collaborate on analytical protocols, conduct lab investigations, and maintain documentation and equipment.

Lead global MSAT technology transfer and process validation for late-stage and commercial biologics. Drive site-to-site transfers, develop global templates/protocols (PPQ, PQ, batch records), perform gap/risk analyses and mitigation, analyze process data and annual reviews, support regulatory CMC documentation and inspections, and mentor junior engineers.

The EHS Specialist will ensure compliance with environmental, health, and safety regulations, conduct training, investigate incidents, and maintain necessary records within the organization. Responsibilities include monitoring compliance, reporting, and facilitating a safe working environment for all employees.

The Associate Director of Enterprise Integration leads integration strategy, establishes governance, and oversees integration capabilities across the enterprise, focusing on architecture, API management, and continuous improvement.

The Director oversees customer data management, ensuring data integrity, governance, and collaboration across commercial systems. Responsibilities include leading data governance initiatives, managing MDM platform transitions, and mentoring data stewards.

The Associate Director provides legal counsel for Regeneron's manufacturing division, focusing on contracts, trade controls, and compliance with regulatory laws.

The AI Staff Engineer will design data flows and AI solutions, lead technical engagements, and deliver production-ready systems while ensuring scalable and maintainable designs. They will also translate business needs into effective technical solutions and build relationships with stakeholders.

The Senior Director of Manufacturing leads cGMP production, ensuring quality and cost-effectiveness while managing staff and compliance with regulations. This role oversees manufacturing operations and develops strategies aligned with site objectives.

The MS&T Engineer III leads project coordination, manages technical documentation, drives process improvements, and collaborates cross-functionally to ensure compliance and successful technology transfers.

The Sr Manager, Quality will oversee the Quality functions within Biologics Analytical Services, ensuring compliance, data integrity, and quality across various programs, while also leading teams and promoting continuous improvement.

The Lead Software Engineer will design, build, and maintain telecom software, focusing on network performance, security, and user experience. Responsibilities include coding, testing applications, performance optimization, protocol implementation, and collaboration with cross-functional teams.

The role involves leading federal business development strategies, managing opportunities, mentoring staff, and collaborating on proposals to achieve growth targets.

The Lead IT Product Manager will define the vision and strategy for product portfolios, manage demand, oversee vendor relationships, and ensure cross-functional coordination while mentoring junior team members and analyzing business value.