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 Lead Engineer will oversee technology transfer for cell culture and purification processes at the Lonza Singapore production facility, manage ongoing process monitoring, investigate process issues, and provide technical mentorship.

The Senior Specialist is responsible for leading technical reviews, ensuring compliance, mentoring junior staff, and supporting quality investigations related to assays and technologies in a life sciences environment.

The Senior Analyst QC will execute and interpret analytical methods, ensure compliance with cGMP, support investigations, and mentor team members in a biochemistry QC lab setting.

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

As a Senior Engineer, you will manage CAPEX projects, develop plans, ensure safety and efficiency, and enhance site operations.

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

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

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

Lead technology transfer of manufacturing processes for cell & gene therapy while providing technical oversight during GMP runs and continuous improvements.

The AnT1 Trainee will undergo a 15-month training program involving analysis, documentation, lab support, and adherence to cGMP, aimed at building competencies in quality control within biopharmaceuticals.

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

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

The QA Specialist ensures compliance with quality standards in a biotech facility, manages quality assurance activities, leads investigations, and supports regulatory audits.

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

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 trainee will receive structured training in MSAT tech transfer support, including documentation management, communication with project teams, and understanding cGMP requirements in biopharmaceuticals.

The Biotechnologist supports the manufacturing of therapeutic cell products in a CGMP environment, involving production activities and compliance with clean room standards.

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