Top Biotech Jobs in Boston, MA

The role involves lab-based process development for guide-RNA drug substances, focusing on synthesis, purification, and collaboration with cross-functional teams.

The role involves developing LNP processes for manufacturing, conducting process characterization studies, and collaborating on Phase 3 readiness. Requires significant lab experience and strong communication skills.

The Principal Engineer will lead tech transfer and manufacturing processes for gene editing products, oversee manufacturing campaigns, and collaborate with various teams to ensure quality and regulatory compliance.

Lead quality operations, drive continuous improvement, oversee non-conformance evaluations, mentor teams, and influence quality culture in manufacturing.

The Reconstruction Sales Representative will drive sales of orthopedic products, build relationships with surgeons, and provide clinical case support in the operating room.

The Global Marketing Manager will grow the Shoulder Repair business through new product development and global strategy while collaborating with local marketing teams to achieve revenue targets.

The role involves delivering data-driven insights on market dynamics and competitive positioning through advanced analytics and market modeling. It supports strategic planning and partners with various teams to inform executive decisions.

The Okta Engineer will support the IAM program through Okta administration, configuration, and enhancement of security practices, collaborating with teams to manage integrations and automations.

The Senior Clinical Trial Manager oversees clinical budgets, develops monitoring plans, drives enrollment, optimizes CRA performance, and maintains study integrity. They also manage relationships with stakeholders and mentor team members.

The Senior Clinical Research Associate will oversee clinical trials, ensuring compliance, maintaining data integrity, and preparing study documentation while collaborating with investigators and site staff.

Oversee and manage clinical trial activities, ensuring adherence to protocols, regulatory requirements, data integrity, and participant safety. Conduct site visits, provide support, and maintain relationships with stakeholders.

The Director oversees real-world studies, providing biostatistical expertise, mentoring staff, ensuring methodological rigor, and engaging in strategic communications, while enhancing pharmaceutical development through innovative methodologies.

The role involves applying computational skills to analyze omics data, collaborate with scientists, and support clinical decisions through data integration.

The Senior Director will lead biologics manufacturing innovations, drive technology transfers, and manage a global team while enhancing product performance and complying with regulations.

The Manager of Chargeback Operations manages membership processes, collaborates across teams, ensures compliance, oversees contract operations, and drives process optimization.

The Principal Analyst will oversee technical operations for Vertex's revenue management platforms, ensuring system integrity, optimizing workflows, and supporting pricing strategies across the organization.

The Director of Order Management Operations is responsible for leading daily operations of the Care Manager team, ensuring effective support for customer needs and optimizing processes within the Heme Business Unit. Strong leadership and cross-functional collaboration are essential to enhance team performance and ensure compliance with operational objectives.

The Associate Director leads cross-domain data initiatives, ensuring high-quality data delivery, establishing data management standards, and mentoring team members.

The Associate Director, PV Scientist will lead safety surveillance, manage risk plans, oversee aggregate safety reporting, and ensure compliance with global regulations while mentoring a team.

The Scientific Director, Pathology will provide veterinary toxicologic pathology expertise, lead nonclinical safety studies, and contribute to drug development strategies at Biogen.

The Master Scheduler is responsible for managing integrated production schedules, balancing capacity and inventory levels, and ensuring on-time delivery. This role includes developing schedules, interfacing with supply chain and engineering, and providing metrics to program leadership.

Manage and control system-level integration and testing requirements, develop test procedures, and mitigate technical risks in a multidisciplinary environment.

Develop tailored cybersecurity solutions, assess vulnerabilities, and mentor engineers while collaborating in multidisciplinary teams.

The Automation Engineer III designs and implements automation systems for manufacturing, provides technical support, and ensures compliance with GMP and FDA regulations.

The HR Leader develops policies and programs related to staffing, employee relations, performance management, and compliance, ensuring alignment with business objectives.

The Director of Pricing will manage global pricing strategies, lead pricing reviews, advise on pricing strategies, and align pricing with business goals.