Oversee Quality Assurance activities, review documents, support inspections, manage compliance, and drive continuous improvement initiatives in a biopharmaceutical setting.

Join the Cell and Gene Therapy Manufacturing team to perform cGMP manufacturing activities, operate equipment, and ensure compliance with quality standards.

The Senior Accountant will oversee financial reporting, manage accounting records, and ensure compliance with regulations and policies. Responsibilities include preparing financial statements, coordinating audits, and mentoring junior staff.

The QA Specialist will support Quality Assurance activities, ensure compliance, oversee product status, conduct investigations, and support audits.

Oversee QC operations, ensuring compliance with cGMP, managing personnel development, and maintaining product release timelines and audit readiness.

As an Intern, you'll gain hands-on experience in pharmaceutical manufacturing, adhering to cGMP, and supporting daily operations while developing problem-solving skills.

As a Biotechnologist, you will perform GMP manufacturing operations, equipment handling, and apply aseptic techniques in a cleanroom environment while executing chromatography and maintaining lab standards.

The QA Specialist supports daily quality assurance tasks, reviews documentation, leads small projects, ensures compliance with GMP, and participates in audits and investigations.

The QA Specialist will oversee Quality Assurance activities, manage product status, investigate deviations, prepare release documentation, and ensure compliance in a GMP facility.

The trainee will conduct analytical testing for cell culture and purification teams, document results per GMP regulations, and perform general lab support duties.

Supervise day-to-day QA activities at a biotech facility, ensure compliance with cGMP, support audits, and lead special projects.

The Technical Specialist is responsible for managing manufacturing operations, including operational readiness, deviation investigations, and supporting continuous improvement initiatives.

The Associate Manager, QC oversees biochemistry method transfer to QC, ensuring compliance and operational excellence, while supervising lab activities and personnel development.

As a trainee in Quality Control, you'll perform testing and analysis of products, maintain documentation according to cGMP, and support lab operations.

As a Biotechnologist, you'll handle GMP manufacturing, operate bioreactors, execute chromatography, and maintain lab standards while working on therapeutic protein production.

As a Biotechnologist, you'll perform GMP manufacturing operations and maintain facility standards while applying aseptic techniques and operating bioreactors.

The trainee will work in Development Services focusing on cell culture, purification processes, and analytical testing, adhering to cGMP standards.

The Biotechnologist Trainee will manufacture therapeutic proteins under cGMP, perform basic lab tasks, equipment monitoring, and maintain facility standards in a clean room environment.

As a CCP Trainee in the MSAT USP team, you'll assist with pre-campaign preparations, process monitoring, post-campaign reviews, and support commercialization efforts while collaborating with cross-functional teams.

The Senior Process Engineer will oversee technology transfer, process optimization, compliance, and documentation in the CGT division, ensuring GMP standards and collaborating with teams and clients.