Intern, QC

Today, Lonza is a global leader in life sciences operating across five continents. While we work in science, there’s no magic formula to how we do it. Our greatest scientific solution is talented people working together, devising ideas that help businesses to help people. In exchange, we let our people own their careers. Their ideas, big and small, genuinely improve the world. And that’s the kind of work we want to be part of.

Did you know that we are the 1st biologics contract manufacturer in Singapore? We offer you exposure to upcoming biotech and established pharmaceutical companies and to the manufacturing technology needed to produce mammalian treatments and cell therapies of tomorrow. Our global manufacturing network is recognized for its reliable, high-quality services, regulatory track record, global footprint, innovative technology platforms and extensive experience – we, in Singapore are proud to be part of this global network.

Job Scope

• Environmental and/or Raw Material Sampling in accordance with cGMP and Lonza policies and procedures
• Autoclave Quality Control material (training will be provided)
• Assist in Laboratory Items Purchasing
• Complete documentation including logbooks, test request preparation and sample distribution
• Assist with Quarterly and Yearly Retain inspection (adhoc basis)
• Discard old samples and hazardous wastes from laboratory (safety training will be provided)
• Maintain inventory levels of consumables and media items
• Communicate all problems and/or observations to QC Supervisor
• Perform applicable Housekeeping tasks
• Maintain own training records for all responsibilities associated with this role
• Perform tasks with careful attention to detail
• Water sampling (complete technical training will be provided)
• Biosafety cabinet cleaning (complete technical training will be provided)

Job Requirements

• Diploma/ Degree in a relevant science discipline (Biotechnology, Pharmaceutical Sciences, Biomedical Engineering) preferred
• Strong interpersonal skills
• Effective verbal and written communication skills
• Systematic
• Analytical Skills
• Positive team player (demonstrate dependability, initiative and ability to work well within a team)
• Attendance and punctuality
• Quality of work
• Prepared to perform shift work when required
• Display a reasonable understanding of cGMPs and Compliance after the required training
• Display a solid understanding of the technical process and workflow of daily job activities as it pertains to equipment and processes after the required training
• Demonstrate eagerness to learn and perform additional tasks in the laboratory