Top Biotech Jobs in Chicago, IL

The Senior Quality Engineer II ensures quality assurance for IVD devices and LDT products, oversees compliance, manages risk, and participates in audits.

The Senior Integration Analyst will deploy and support Epic integrations, particularly focusing on Epic Aura, ensuring smooth data exchange and compliance with standards.

The role involves developing customer-facing reports, providing insights, managing analytics for health systems, and collaborating cross-functionally to enhance operational efficiency.

The Software Engineer will enhance developer experience by creating efficient tools for production releases and streamline workflows while collaborating with various teams.

The Senior Product Manager, Retention will enhance customer engagement and retention by leveraging data and cross-functional collaboration to optimize user experiences and lifecycle messaging.

The Chief Operating Officer will lead operational execution and manage delivery teams, drive company-wide operating rhythms, and partner closely with the CEO and leadership team to scale the organization and enhance operational effectiveness.

The Lead Clinical Research Associate oversees clinical trial sites, ensuring compliance with regulations and protocols while mentoring CRAs and collaborating with teams to execute trials effectively.

The Site Specialist II role involves supporting regulatory documentation, ensuring compliance for site activation, and collaborating with stakeholders for optimal study performance.

The Digital Media Buyer develops and implements digital advertising campaigns for patient recruitment, optimizing performance and collaborating on content creation.

The program accelerates professional development through training and business assignments in engineering, innovation, and technology.

The Sr. Buyer leads complex procurement projects, conducts cost analysis, negotiates contracts, manages supplier relationships, and ensures compliance with regulations while mentoring junior buyers.

As a Production Supervisor, lead resin processing operations, ensure safety and quality compliance, troubleshoot issues, and optimize workflows, while managing a team and maintaining production records.

Manage TMF documentation transitions within Novartis for M&A and licensing projects, ensuring compliance and process improvement in clinical document management.

The RLT Associate Director will drive strategic account engagement, manage relationships with healthcare systems, and execute business plans to optimize Radioligand Therapies adoption.

The Associate Director will manage strategic initiatives within neuroscience accounts, building partnerships and executing account business plans to optimize product access for patients.

As Senior Portfolio Manager, lead strategy and innovative programs for Hip Revision surgery, collaborating with surgeons, sales force, and stakeholders to enhance patient outcomes and drive product development.

As a Sales Representative for Craniomaxillofacial products, you will promote and sell in the field, conduct product evaluations, and maintain strong customer relationships.

The Program Manager will oversee Stryker's Global Trade Legal & Compliance governance framework, ensuring compliance with trade regulations through policies, training, and communication initiatives.

As a Senior Project Controls Engineer, you will manage project schedules, costs, and reporting for biomanufacturing projects, while collaborating with various stakeholders and ensuring high-quality deliverables.