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.

As a Biotechnologist, you'll support GMP manufacturing of therapeutic proteins by operating mammalian cell cultures, performing downstream purification, and maintaining cGMP standards.

Lead technology transfer of manufacturing processes, provide technical oversight during GMP runs, and drive continuous improvements. Collaborate across teams and support regulatory inspections.

The QA Expert will oversee Quality Assurance activities, support audits, lead projects, and mentor junior team members within a GxP manufacturing environment.

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.

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

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.

The QC Analyst will conduct analytical testing, document results, troubleshoot methods, support lab operations, and ensure compliance with quality systems.

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

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.

Lead and supervise electrical engineers and technicians to perform maintenance, troubleshooting, repairs, and preventive maintenance in a cGMP manufacturing environment. Manage electrical and fire alarm systems, supervise vendors, ensure GMP/EHS compliance, train staff, and lead root cause analyses to minimize production disruption.

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

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

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

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

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 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.