The QA Specialist supports daily quality assurance tasks, reviews documentation, leads small projects, ensures compliance with GMP, and participates in audits and investigations.

As an Intern, you'll gain hands-on experience in pharmaceutical manufacturing, adhering to cGMP, and supporting daily operations while developing problem-solving skills.

Join the Cell and Gene Therapy Manufacturing team to perform cGMP manufacturing activities, operate equipment, and ensure compliance with quality standards.

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

The QA Specialist will support Quality Assurance activities, ensure compliance, oversee product status, conduct investigations, and support audits.

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

The Senior Analyst in QC tests environmental and product samples, documents results, ensures compliance with cGMP, and leads investigations.

The QA Intern will assist in various Quality Assurance activities, including reviewing documents, supporting batch records, and data entry in a GMP environment.

The Associate Manager will oversee QA operations, ensuring compliance with SOPs, coordinating between departments, driving continuous improvement, and managing team performance.

As an Operational Buyer, you will ensure the procurement and qualification of raw materials, manage vendor performance, and handle supplier qualification processes.

The Systems Specialist maintains lab computerized systems, supports software installations, prepares validation protocols, and ensures compliance with regulatory expectations.

As a CCP Trainee in MSAT, assist in executing process validation activities, develop and execute PV protocols, and support data compilation and investigations within a GMP biotech facility.

The Senior Accountant will oversee financial reporting, manage accounting records, and ensure compliance with regulations and policies. Responsibilities include preparing financial statements, coordinating audits, and mentoring junior staff.

As a CCP Trainee in the MSAT USP team, you'll assist with pre-campaign preparations, process monitoring, post-campaign reviews, and support commercialization efforts while collaborating with cross-functional teams.

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

The QA Specialist will oversee Quality Assurance activities, manage product status, investigate deviations, prepare release documentation, and ensure compliance in a GMP facility.

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

Lead the transfer of cell culture processes into production, support process monitoring, conduct investigations, and ensure robust manufacturing at Lonza Singapore.

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

The trainee will work in Development Services focusing on cell culture, purification processes, and analytical testing, adhering to cGMP standards.