3 manufacturing jobs found

Repligen Overview Repligen is seeking a Process Engineering Intern to support the Waltham Process Engineering team during a summer internship. This role focuses on manufacturing process improvements on OPUS Chromatography products. The intern will work onsite in Waltham under the guidance of the Process Engineering Manager, contributing to experimental design, testing, and potential process implementation within an 8-12 week timeframe. Responsibilities Research and evaluate methods to achieve faster glue set and cure times. Design and execute experiments, including a Design of Experiments (DOE), to test and compare potential solutions. Analyze experimental results and document findings in a test summary report. Support qualification of an optimal solution and assist with implementing the updated process into manufacturing as a standard operating procedure. Other assigned duties as required. Qualifications Must be enrolled in an engineering, or...

Alkermes, Inc. The Sr. Manager position within Clinical Supply Chain leads end-to-end supply chain management on multiple clinical programs as part of a growing, dynamic Pharmaceutical Development organization. They work closely as the key point of contact with Clinical Operations, Regulatory Affairs, Quality, Internal & External Manufacturing, and other Clinical Supply Chain personnel leading supply activities for complex programs that may require multinational interactions. In addition, they coordinate and lead supply activities with both internal and external partners. The successful candidate will thrive in a highly collaborative team environment to ensure the successful development of new drugs. Responsibilities Prepare, update and monitor program budgets and ensure financial Key Performance Indicators (KPIs) and relevant cost saving targets Proactively lead clinical program supply strategy ensuring trial design, enrollment timeline, manufacturing availability and...

Alkermes, Inc. Position Summary: The Process Development Technician supports the execution of experimental studies to develop well-understood, robust oral solid dosage (OSD) manufacturing processes. Key responsibilities include equipment setup, cleaning, troubleshooting, execution of experiments, and data collection to identify and implement process and equipment improvements that reduce waste and increase process reliability. This role plays a key part in maintaining GMP standards within the pilot facility and supporting the manufacture of clinical supplies. Responsibilities: Support the set up and operation of a new GMP clinical manufacturing suite with a broad range of processing capability and technology approaches.Operate, maintain, and troubleshoot a variety of process equipment, rapidly assimilating and applying new technologies as introduced.Perform equipment and room cleaning in compliance with established housekeeping and GMP standards.Assist in...