Search the 5 jobs at PepGen

Senior Specialist, Quality Assurance responsible for quality review of production and testing of clinical trial materials at external manufacturing site. Tasks include review and approval of batch records, analytical testing protocols, coordination of disposition activities, ensuring compliance with regulations, and supporting regulatory filing activities.

The Associate Director of Analytical Development at PepGen will lead analytical projects, support regulatory filings, collaborate with internal and external teams, manage testing activities, and mentor junior scientists. This role requires a Ph.D. in Chemistry or related field with over 5 years of experience in analytical development and project leadership.

The HR coordinator at PepGen will be responsible for candidate experience, onboarding logistics, maintaining employee data, audit reports, L&D administration, and ad-hoc projects. Must have experience in fast-paced environments, proficiency in Microsoft Office, attention to detail, and excellent communication skills.

The Associate Director/Director of Data Management at PepGen is responsible for overseeing and directing clinical data management activities, managing external service providers, and leading data cleaning activities. The role requires a master's degree or extensive work experience in the pharmaceutical industry, project management skills, and proficiency in regulatory standards and therapeutic areas.

The Scientist, Analytical Development at PepGen will lead method development and provide analytical support for drug discovery activities, focusing on neuromuscular diseases. Responsibilities include method development, analytical support, protocol writing, and equipment maintenance. Requires a Ph.D. in Chemistry or related field with 1+ years of experience, strong HPLC and MS skills, and familiarity with cGMPs/GLP.