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

Lead a technical team in bioprocessing, manage client relationships, support product integration into therapy development, and deliver presentations for industry engagement.

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

As a Process Validation Trainee, assist in executing process validation activities, develop protocols and reports, support data compilation and investigations.

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

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

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

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

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

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

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

The Technical Investigator leads investigations into production deviations, conducts root cause analysis, defines CAPAs, and collaborates with various stakeholders. Responsibilities include writing deviation reports and preparing for audits.

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

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

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

The Biotechnologist Trainee is responsible for manufacturing therapeutic proteins under cGMP conditions, performing lab tasks, equipment monitoring, and maintaining high facility standards while learning strict manufacturing protocols.

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

In this role, you will perform GMP manufacturing operations, handle equipment, maintain lab standards, and apply aseptic techniques in a team-oriented environment.