Trainee, QA (CGT)

Singapore, Tuas Singapore

Lonza is the pioneer and world leader in the CDMO industry operating across 5 continents, setting the pace with cutting-edge science, smart technology and lean manufacturing. We turn our customers' break-through innovations into viable therapies and manufacture the medicines of tomorrow. At the heart of every scientific breakthrough are talented individuals collaborating to develop solutions that empower businesses to improve lives. 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.

Join our best-in-class high performance Integrated Biologics team at our Tuas site in Singapore to gain unparalleled exposure to cutting-edge biotechnology and innovation, and make a difference from day one. Learn new skills and capabilities, and grow your career with us in manufacturing therapeutic proteins under cGMP conditions. Find out more about what a life at Lonza in Singapore could look like for you by watching this short video.

The Career Conversion Program (CCP) training period lasts for 15 months. Structured on-the-job training (OJT) will be provided and conducted at the participating companies to facilitate the application of learning and to ensure that individuals acquire necessary competencies to perform at their job.

The QA Trainee will support day-to-day Quality Assurance activities in accordance to the respective Quality Areas.

Job Scopes

Support day-to-day Quality Assurance activities in accordance with approved SOPs / Policies for a multi-product, cGxP contract manufacturing facility

Management of GMP document lifecycle in Documentation Management System including archiving and inactive records

Issuance of controlled documents (e.g Batch records and Logbooks)

Display a good level of problem solving ability by analyzing and interpreting data and puts forward new ideas based on scientific knowledge or field experience

Detect non-compliance with cGxP and cGDP requirements and provide guidance on GDP corrections

Generally provide basic compliance support to staff in all departments

Demonstrate appropriate interpersonal skills that encourage collaboration of individuals or teams to meet objectives

Uphold data integrity principle in accordance to Lonza policies. Proactively evaluate, identify and improve data integrity process.

Any other tasks as and when assigned by Supervisor

Requirements

Diploma/ Degree in relevant science discipline (Biotechnology, Pharmaceutical Sciences, Biomedical Engineering etc.)

Strong interpersonal skills

Effective verbal and written communication skills

Meticulous eye for detail

Systematic

Positive team player

Every day, Lonza's products and services have a positive impact on millions of people. For us, this is not only a great privilege, but also a great responsibility. How we achieve our business results is just as important as the achievements themselves. At Lonza, we respect and protect our people and our environment. Any success we achieve is no success at all if not achieved ethically.

People come to Lonza for the challenge and creativity of solving complex problems and developing new ideas in life sciences. In return, we offer the satisfaction that comes with improving lives all around the world. The satisfaction that comes with making a meaningful difference.

Reference: R72795

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