The Scientist II in Analytical Development analyzes drug substances and products using HPLC, GC, and other methodologies. Responsibilities include method development, data reporting, regulatory submissions support, and maintaining lab standards. They collaborate internally and externally to ensure compliance and scientific advancement.

The Key Account Manager position involves building and sustaining relationships with healthcare providers, driving sales and business strategies, addressing drug access issues, and providing training on pharmaceutical products. The role requires extensive travel within the assigned territory and collaboration with various stakeholders to optimize patient care and achieve sales targets.

The Senior Manager, Quality Assurance - GxP (GCP) manages QA functions focused on GCP compliance. Responsibilities include conducting audits, supporting inspection readiness, and collaborating with various teams to ensure adherence to regulations and SOPs. The role also involves mentoring direct reports and developing QA-related processes.

The Office Manager provides administrative support to the VP/GM and senior executives, managing calendars, coordinating meetings, arranging travel, processing expense reports, and maintaining office operations. The role requires collaboration with local and global teams on various administrative issues.

The Artwork Specialist/Senior Specialist is responsible for managing artwork updates, ensuring regulatory deadlines are met, and coordinating artwork changes with various internal and external stakeholders. The role includes monitoring project timelines, managing quality records, and facilitating communication across teams to ensure compliance and timely delivery of projects.

The Office Manager at PTC Therapeutics will provide high-level administrative support to senior management, coordinate meetings, manage travel arrangements, process expense reports, and maintain office operations. The role involves liaising with IT and local accounting while participating in event coordination and CRM management. Excellent organizational skills and proficiency in Microsoft Office are essential.

The Director of Contract Strategy and Operations oversees the operational aspects of contract strategies in the Market Access team, ensuring compliance, managing the contract lifecycle, and optimizing revenue through data-driven insights. This role requires collaboration with cross-functional teams and external stakeholders, focusing on contract negotiations, pricing policies, and process improvements in alignment with strategic goals.

The Machine Learning Engineer will design, implement, and maintain AI solutions to enhance drug development and business intelligence in the pharmaceutical industry. They will collaborate with various teams, ensure regulatory compliance, and participate in code reviews to maintain high code quality. Continuous learning about AI/ML techniques and translating technical concepts to non-technical stakeholders are key responsibilities.

The Brand Lead will oversee the launch and growth of a new product related to Phenylketonuria (PKU). Responsibilities include strategic brand leadership, operational execution, stakeholder engagement, and cross-functional collaboration with teams to ensure successful product management and marketing alignment.

The Paralegal will support the legal team by drafting and reviewing contracts, managing the contracts database, ensuring compliance with legal requirements, and performing administrative tasks. They will also assist with legal presentations and filings while maintaining high sensitivity to information.

The Associate Scientist I in Neuroscience conducts scientific experiments for research and drug discovery, focused on identifying New Chemical Entities (NCEs). Responsibilities include executing experiments, troubleshooting, maintaining lab notebooks, and participating in multi-disciplinary teams. The role involves cell-based screenings, data management, and communicating findings to project teams.

The BOG Coordinator supports the PTC Biostatistics and Data Management Department by managing administrative tasks, including contractual and financial documentation, invoicing, and collaboration with internal and external teams to ensure compliance with regulatory standards. Adapting to a fast-paced environment, the coordinator also oversees electronic resources and enhances operational processes.

The Pharmacovigilance Operations Manager oversees the monitoring and reporting of Adverse Event and Serious Adverse Event reports, ensuring compliance with global regulations. Responsibilities include quality control of safety reports, collaboration with vendors, and maintaining the safety database. The position requires working cross-functionally within the organization to ensure adherence to safety protocols and timely reporting.