Jobs at Lonza

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

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

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

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

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.

As a QC Analyst, you will conduct testing and analysis of samples, ensure compliance with SOPs and cGMP, document results accurately, and support lab operations.

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 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 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.

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

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