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.

The Associate Engineer will support validation and maintenance activities for temperature-sensitive equipment, ensure compliance with standards, and assist in new equipment setup.

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

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

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.

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

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.

Lead Engineering operations related to technology transfers and process campaigns, manage manufacturing deviations, and ensure compliance with regulatory standards.

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

The Head of CGT Operations leads therapeutic cell therapy production under cGMP, ensuring safety, compliance, efficiency, profitability, and team development.

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

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.

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

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

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

Lead the transfer of customer manufacturing processes, perform experiments, manage technical documentation, support investigations, and implement process improvements.

The Senior QA Specialist will ensure Quality Assurance compliance, manage deviation investigations, lead audits, and improve quality processes in a biopharmaceutical facility.

The QA Specialist will conduct Quality Assurance activities in a GMP biotech manufacturing facility, support audits, lead investigations, and ensure compliance with SOPs and policies.