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

Provide QA oversight for multi-product GMP biopharma manufacturing: review batch records, approve SOPs/protocols, lead small team and projects, manage deviations, change controls, CAPA, audits, and support regulatory inspections.

Manage key customer relationships and drive sales of endotoxin testing and media products across Singapore and SEA. Identify opportunities, create account action plans, provide field technical support, and report market trends. Requires territory call planning and 25 6% travel for sales, trainings, and meetings.

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

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

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

Lonza seeks fresh graduates in Life Sciences or related fields for various roles, emphasizing problem-solving, communication, and teamwork skills.

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

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

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

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 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.

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

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

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

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

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

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

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

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