The Senior Process Engineer will lead the transfer of cell culture processes, support operations, investigate trends, and ensure compliance with standards.

The QA Specialist will support Quality Assurance activities in a GMP biotech manufacturing facility, ensuring compliance, leading investigations, and coordinating with departments.

Lead multidisciplinary project teams to ensure smooth execution of contracted programs, focusing on customer satisfaction, quality, cost, and timelines.

The Biotechnologist Trainee is responsible for manufacturing therapeutic proteins under GMP conditions, performing laboratory tasks, troubleshooting, and maintaining equipment compliance.

Oversee harmonization projects across global network sites, provide technical support and coaching, and maintain compliance knowledge to improve operational execution.

The intern will support the Technical Writing Team and Planning team by managing documentation, ensuring compliance with GMP, and assisting in data management and project improvement.

Assist MSAT engineers in supporting manufacturing operations by monitoring processes, analyzing data, investigating issues, and managing sample logistics.

The Biotechnologist Intern supports therapeutic protein manufacturing under cGMP conditions, performing laboratory tasks and maintaining facility standards while gaining experience in a biotech environment.

Supports deviation investigation by managing GMP documentation, collaborating with SMEs, performing data mining, and assisting with CAPA implementation.

Provide operational support in the Development Services Department, assisting with laboratory tasks, equipment verification, and housekeeping activities.

The QC Analyst will perform various testing and analysis, ensure cGMP compliance, solve analytical problems, and support laboratory operations.

The Biotechnologist will perform GMP manufacturing operations, handling equipment and troubleshooting, operating bioreactors, and preparing solutions for production while adhering to cGMP standards.

The QC Analyst will perform microbiological tests, analyze samples, document results per cGMP guidelines, and assist with method transfers and validations.

The Communications Manager shapes the site's communication strategy, enhancing employee engagement and managing stakeholder relationships through effective internal and external communication.

The trainee will assist in quality control activities, including equipment verification, documentation, laboratory support, and troubleshooting under supervision.

The role involves microbiology testing, documentation, equipment maintenance, and lab support in compliance with cGMP regulations. Candidates should have a relevant science degree and lab experience.

The Analyst will conduct microbiological and biochemical testing, analyze product quality, document results, support OOS investigations, and assist in lab operations.

Lead complex protein characterization projects using mass spectrometry and other analytical methods, mentor junior staff, and enhance lab processes.

The Intern will support quality control efforts including sampling, documentation, data entry, and maintaining laboratory supplies while adhering to safety and regulatory protocols.

Oversee transfer of biochemistry analytical methods into QC, ensuring operational excellence, regulatory compliance, and supervising lab operations.