Jobs at Lonza

The Site HR Head leads HR activities aligning with business goals, manages talent development, employee relations, and team performance in Singapore.

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

The Head of CGT Operations leads CGT manufacturing under cGMP, ensuring compliance, operational performance, and financial execution, while guiding a management team and developing talent.

The QA Specialist ensures compliance with GMP standards in manufacturing, reviews quality documents, leads investigations, and manages relationships with teams and partners.

The trainee will receive structured on-the-job training in technology transfer, document management, and collaboration with project engineers in the biopharmaceutical industry.

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 Principal Expert leads the data science strategy for MSAT, establishes best practices, delivers high-impact initiatives, and mentors teams in a regulated environment.

The Biotechnologist Trainee will learn to perform procedures in a GMP setting, monitoring equipment, conducting basic lab tasks, ensuring facility standards, and developing process expertise.

The QC Analyst in Biochemistry will conduct analytical testing in compliance with quality regulations, support lab operations, troubleshoot methods, and assist in investigations while training others.

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

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.

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

The Associate Manager in Process Development leads a team in downstream purification activities, ensuring compliance, coaching members, and handling projects and lab work.

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

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.

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.

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 will perform QA activities including batch record review, product release documentation, deviation investigations, CAPA monitoring, and supporting regulatory inspections in a GMP facility.