Top Operations Jobs in Boston, MA

As a Senior Staff Engineer, you will manage product development, lead projects in manufacturing, provide technical expertise, mentor junior staff, and support CMC strategy development.

Lead Regulatory Affairs operations, provide project management support, monitor KPIs, manage budget, and facilitate decision-making processes.

Lead global regulatory strategies and teams for complex pharmaceutical projects, ensuring compliance and effective communication with stakeholders. Oversee regulatory submissions and initiatives, managing risks and developing solutions to regulatory challenges.

The Cell Therapy Specialist will execute manufacturing operations for patient therapies, ensuring compliance with cGMP and performing cell culture techniques and supporting operations in a cleanroom environment.

The Senior Validation Engineer will manage validation documents, oversee equipment qualification protocols, ensure compliance with FDA regulations, and analyze validation data.

Lead regulatory CMC strategies for cell therapies, ensuring compliance with regulations, mentoring teams, and influencing project teams during drug development.

The Associate Engineering Fellow will lead complex programs in process engineering, focusing on developing robust manufacturing processes and collaborating closely with cross-functional teams to optimize pharmaceutical production.

The Associate Director leads global regulatory strategies for complex projects, ensures compliance, provides strategic advice, and oversees submissions to health authorities.

The Medical Director leads global safety for pharmaceutical products, manages safety assessments, and communicates with regulatory authorities while ensuring compliance with safety standards.

The Lab Asset Data Manager ensures accurate laboratory asset data across teams, supports system implementation, and enhances operational efficiency through data management and collaboration.