As a Calibration Technician, you'll execute calibration and repair activities, troubleshoot instruments, and maintain compliance with GMP requirements, documenting all work accurately.

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

Lead the transfer and monitoring of purification processes in manufacturing, ensure compliance, and provide technical mentorship while handling investigations and audits.

As a Technical Expert, lead manufacturing projects in cell and gene therapy, ensure compliance with cGMP, and drive cross-functional improvements.

The QA Trainee will support Quality Assurance activities, manage GMP documents, provide compliance support, and uphold data integrity.

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

The role involves leading portfolio governance and PMO processes, ensuring project execution standards, managing resource allocations, and coordinating with other PMO teams.

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

The Procurement Change and Training Advisor will lead training initiatives, manage change processes, and enhance procurement practices through strategic collaboration and curriculum development.

The Senior QA Specialist oversees Quality Assurance activities for a GxP facility, ensuring compliance, managing customer interactions, and leading quality improvement projects.

The Biotechnologist Trainee will perform GMP manufacturing tasks, including equipment monitoring, basic laboratory procedures, and maintaining cleanroom standards while working under supervision.

The role involves providing QA oversight in a GMP facility, reviewing and approving documentation, leading deviations and CAPAs, troubleshooting quality issues, and ensuring process improvements and compliance.

The Biotechnologist will execute Cell Therapy production under cGMP conditions, performing tasks like culture preparation, harvesting, filling vials, and maintaining cleanroom standards.

The role involves providing QA oversight, reviewing protocols and reports, managing QA processes, and developing skills to support internal and external audits.

The QA Specialist supports Quality Assurance activities, ensuring compliance, reviewing batch records, guiding investigations, and overseeing product statuses.

The Analyst 2 will execute biochemical tests, document results, support lab operations, manage QC samples, and enhance operational efficiency.

The role involves liaising with vendors for equipment, creating qualification documents, and ensuring equipment's timely release while maintaining data integrity.

As a QC Analyst, you will perform various analyses, document results, troubleshoot methods and equipment, and ensure compliance with cGMP.

The Biotechnologist will manufacture therapeutic cell products under CGMP conditions, including cell culture, aseptic processing, and documentation, in a cleanroom environment.

As a Biotechnologist, you will perform GMP manufacturing operations, maintain facility standards, handle bioreactors, and utilize process control systems.